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Showing posts with label Advanced. Show all posts
Showing posts with label Advanced. Show all posts

Saturday, August 10, 2013

Symptoms of Advanced Stage Prostate Cancer

Prostate cancer is a kind of dangerous diseases to be afraid of by almost all of adult men. Well, since it is particularly affecting the system of reproduction and even digestion, therefore, you may imagine that it will simply damage the patients' life. Although it is known that this type of cancer is often producing certain symptoms, in fact, there are also many people that don't feel any signs at all just before being diagnosed. But if you notice well, there are several matters that can indicate that you are one of the next prostate cancer just by only seeing several signs and also noticing your lifestyle.

Here are several things that you should aware so much, since they can be several undetected symptoms of prostate cancer. Just check them out.

Frequent Urination

Well, the first thing that you should consider well is regarding the dying for a pee, particularly at night. It is actually something which is common to be experienced if your water consumption tends to be higher. But of course, if you think you are not drinking too much before sleeping, surely, it is something that you should pay attention. Besides, another symptom is that you find it rather difficult when starting to pee or even you feel it pain. Yes, if you have experienced such things, you should then better visit the doctor.

Blood in Your Urine

In a higher level, you will find that there is blood in your urine. Of course, there are actually several other diseases that have such symptoms like reproduction infection. Therefore, if you already have such experiences, it is much better also to go to the doctor to ask for any diagnose.

Erectile Difficulties

Another symptom that you swill find while being a patient of prostate cancer is about the disorder within your sexual organ. One of them is the erectile difficulty. Many adult men then assume and decide to consume such vitality medicine to solve this problem. It is surely no matter at all if you are normal, but if it is then a symptom of prostate cancer, it will be more dangerous. Again, going to the doctor firstly before consuming something is much better.

Feeling Pain While Ejaculating

Well, if you think your sexual activities with your wife has been disturbed for something unpleasant like pain while ejaculating, therefore, you should pay attention more. Almost all the disorders occurred within the prostate will produce such symptom, so that being careful is really important.

Backache, Sore Hip and Thighs

You should not underestimate the pain on several areas of your body, including the back, hip and thighs. Yes, although you may think that it is not so much different with the effects of tiredness or something, surely, it is better then to ask any diagnose from the doctor, since it can be one of the symptoms of prostate cancer.

Overall, the symptoms explained above are not so much different with any insignificant diseases. It is probably being the main reason why many people prefer ignoring them. Mainly for you the men above the 50 years old who are more susceptible for the prostate cancer, you should then regularly check your health, particularly if you have experienced such symptoms.

Wendy Hood Photo Wendy H. Hood is a blogger who interested on prostate cancer . More information about this topic can be found online on her website.

View the original article here

Symptoms of Advanced Stage Prostate Cancer

Prostate cancer is a kind of dangerous diseases to be afraid of by almost all of adult men. Well, since it is particularly affecting the system of reproduction and even digestion, therefore, you may imagine that it will simply damage the patients' life. Although it is known that this type of cancer is often producing certain symptoms, in fact, there are also many people that don't feel any signs at all just before being diagnosed. But if you notice well, there are several matters that can indicate that you are one of the next prostate cancer just by only seeing several signs and also noticing your lifestyle.

Here are several things that you should aware so much, since they can be several undetected symptoms of prostate cancer. Just check them out.

Frequent Urination

Well, the first thing that you should consider well is regarding the dying for a pee, particularly at night. It is actually something which is common to be experienced if your water consumption tends to be higher. But of course, if you think you are not drinking too much before sleeping, surely, it is something that you should pay attention. Besides, another symptom is that you find it rather difficult when starting to pee or even you feel it pain. Yes, if you have experienced such things, you should then better visit the doctor.

Blood in Your Urine

In a higher level, you will find that there is blood in your urine. Of course, there are actually several other diseases that have such symptoms like reproduction infection. Therefore, if you already have such experiences, it is much better also to go to the doctor to ask for any diagnose.

Erectile Difficulties

Another symptom that you swill find while being a patient of prostate cancer is about the disorder within your sexual organ. One of them is the erectile difficulty. Many adult men then assume and decide to consume such vitality medicine to solve this problem. It is surely no matter at all if you are normal, but if it is then a symptom of prostate cancer, it will be more dangerous. Again, going to the doctor firstly before consuming something is much better.

Feeling Pain While Ejaculating

Well, if you think your sexual activities with your wife has been disturbed for something unpleasant like pain while ejaculating, therefore, you should pay attention more. Almost all the disorders occurred within the prostate will produce such symptom, so that being careful is really important.

Backache, Sore Hip and Thighs

You should not underestimate the pain on several areas of your body, including the back, hip and thighs. Yes, although you may think that it is not so much different with the effects of tiredness or something, surely, it is better then to ask any diagnose from the doctor, since it can be one of the symptoms of prostate cancer.

Overall, the symptoms explained above are not so much different with any insignificant diseases. It is probably being the main reason why many people prefer ignoring them. Mainly for you the men above the 50 years old who are more susceptible for the prostate cancer, you should then regularly check your health, particularly if you have experienced such symptoms.

Wendy Hood Photo Wendy H. Hood is a blogger who interested on prostate cancer . More information about this topic can be found online on her website.

View the original article here

Wednesday, July 10, 2013

Study Examines Spiritual Support For Patients With Advanced Cancer

Main Category: Cancer / Oncology
Article Date: 08 May 2013 - 2:00 PDT Current ratings for:
Study Examines Spiritual Support For Patients With Advanced Cancer
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JAMA Internal Medicine Study Highlights

A study by Tracy A. Balboni, M.D., M.P.H., of the Dana-Farber Cancer Institute, Boston, and colleagues suggests that spiritual care and end-of-life (EoL) discussions by the medical team may be associated with reduced aggressive treatment.

The study included 343 patients with advanced cancer. EoL care in the final week included hospice, aggressive EoL measures (care in an intensive care unit, resuscitation or ventilation), and ICU death.

Patients reporting high spiritual support from religious communities were less likely to receive hospice (adjusted odds ratio [AOR], 0.37), more likely to receive aggressive EoL measures (AOR, 2.62), and more likely to die in an ICU (AOR, 5.22), according to the results. The results also indicate that among patients well-supported by religious communities, receiving spiritual support from the medical team was associated with higher rates of hospice use (AOR, 2.37), fewer aggressive treatments ((AOR, 0.23), fewer ICU deaths (AOR, 0.19) and EoL discussions were associated with fewer aggressive interventions (AOR, 0.12).

"In conclusion, terminally ill patients receiving high spiritual support from religious communities receive more-intensive EoL medical care, including less hospice, more aggressive interventions, and more ICU deaths, particularly among racial/ethnic minority and high religious coping patients," the study concludes. "The provision of spiritual care and EoL discussions by medical teams to patients highly supported by religious communities is associated with reduced medical care intensity near death."

Article adapted by Medical News Today from original press release. Click 'references' tab above for source.
Visit our cancer / oncology section for the latest news on this subject. JAMA Internal Med. Published online May 6, 2013. doi:10.1001/jamainternmed.2013.903. Please use one of the following formats to cite this article in your essay, paper or report:

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13 May. 2013. APA

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Monday, July 8, 2013

Study Confirms Adding Chemotherapy To Surgery Improves Survival In Advanced Gastric Cancer

Article adapted by Medical News Today from original press release. Click 'references' tab above for source.
Visit our cancer / oncology section for the latest news on this subject. Disclaimer
Information contained in this press release was provided by the abstract's author and reflects the content of the study. It does not necessarily express ESMO's point of view

References

1. Abstracts from the 15th ESMO World Congress on Gastrointestinal Cancer are published in Annals of Oncology, Volume 24 suppls 4 June 2013 (Ann Oncol 2013 Jun; 24(Suppl 4): 5-130) http://annonc.oxfordjournals.org/content/24/suppl_4.toc

2. Abstract presentation: Thursday, 4 July 2013, 17:25 hrs, Session VII: Gastric Cancer About the ESMO World Congress on Gastrointestinal Cancer The ESMO World Congress on Gastrointestinal Cancer is the premier global event in the field, encompassing malignancies affecting every component of the gastrointestinal tract and aspects related to the care of patients with gastrointestinal cancer, including screening, diagnosis and the latest management options for common and uncommon tumours. It has been endorsed by leading professional societies and organizations.
The ESMO 15th World Congress on Gastrointestinal Cancer has been organized in partnership with ESMO (European Society for Medical Oncology). The Congress is developed and managed by ImedexR, LLC.

ABSTRACT 0007

Adjuvant capecitabine and oxaliplatin (XELOX) for gastric cancer after D2 gastrectomy: final results from the CLASSIC trial
Sung Hoon Noh 1, Sook Ryun Park 2, Han-Kwang Yang 3, Hyun Cheol Chung 1, Ik-Joo Chung 4, Kyung Hee Lee 5, Hyung-Ho Kim 6, Jiafu Ji 7, Jen-Shi Chen 8, Yunni Lim 9, Stella Ha 9, Yung-Jue Bang 3

1 Yonsei University College of Medicine, Seodeamungyu Shinchon-dong 134, Seoul, 2 Research Institute and Hospital, National Cancer Center, Ilsandong-gu, Goyang-si Gyeonggi-do, 3 Seoul National University College of Medicine, Jongno-gu, Seoul, 4 Chonnam National University Hwasun Hospital, Hwasun-Eup, Hwasun-Gun, Jeonnam, 5 Yeungnam University College of Medicine, Nam-gu, Daegu, 6 Seoul National University Bundang Hospital, Seongnam-si, Gyeonggi-do, 7 Beijing Cancer Hospital, Haidian, Beijing, 8 Chang Gung Memorial Hospital, Kwei-Shan Shiang, Taoyuan, 9 Roche Korea Co.,Ltd, Seocho-Gu, Seoul

Background: D2 gastrectomy, which is widely used in East Asia as the preferred surgery for patients with operable gastric cancer, is now recommended in US and European treatment guidelines for gastric cancer. Two phase III trials (ACTS-GC and CLASSIC) have been performed to assess the possible benefits of adjuvant chemotherapy after D2 surgery. ACTS-GC showed a survival benefit with fluoropyrimidine monotherapy after D2 gastrectomy compared with surgery only [Sasako et al. J Clin Oncol 2011;29:4387–93]. The CLASSIC trial compared fluoropyrimidine-oxaliplatin combination therapy (XELOX) with surgery alone; interim results showed that XELOX improved 3-year disease-free survival after D2 gastrectomy compared with surgery only [Bang et al. Lancet 2012;379:315–21]. Improved overall survival was also evident after only 3 years, but the data were immature. We report here the final results from the CLASSIC trial after a median follow-up of 5 years.

Methods: CLASSIC was a multinational open-label randomised phase III trial performed in South Korea, China, and Taiwan. Randomisation was stratified by country and disease stage. Patients with stage II–IIIB gastric cancer who had undergone curative D2 gastrectomy were assigned to adjuvant XELOX (oxaliplatin 130 mg/m2 day 1 plus capecitabine 1000 mg/m2 twice daily days 1-14 q3w) for 8 cycles or surgery alone. The primary endpoint was 3-year disease-free survival. The clinical cut-off date for the prospectively planned final 5-year efficacy analysis was 22 November 2012.

Results: At data cut-off, 103 (20%) patients in the XELOX group and 141 (27%) patients in the surgery alone group had died. This represented a 34% reduction in the risk of death with XELOX versus surgery alone (hazard ratio 0.66, 95% CI 0.51–0.85; p=0.0015 by stratified Cox regression analysis). The 5-year overall survival rate was 78% in the XELOX group and 69% in the surgery alone group (p=0.0029, log-rank test unstratified). 76 (15%) patients in the XELOX group and 135 (26%) patients in the surgery alone group received subsequent, non-protocol-specified anticancer therapies after progression of disease. In the analysis of disease-free survival, 139 (26.7%) patients in the XELOX group and 203 (39.4%) patients in the surgery alone group had relapsed, developed a new gastric cancer or died. This represented a 42% reduction in the risk of an event with XELOX versus surgery alone (hazard ratio 0.58, 95% CI 0.47–0.72; p<0.0001 by stratified Cox regression analysis). The 5-year disease-free survival rate was 68% in the XELOX group and 53% in the surgery alone group (p<0.0001, log-rank test unstratified).

Conclusion: The final analysis of the CLASSIC trial, after a median follow-up of 5 years, supports the findings from the primary analysis performed 2 years earlier. Adjuvant XELOX after curative D2 gastrectomy improves overall survival compared with surgery alone and should be considered as a standard treatment option for patients with operable gastric cancer.

ESMO

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Thursday, June 20, 2013

Avastin Can Lengthen The Lives Of Advanced Cervical Cancer Patients

Editor's Choice
Main Category: Cervical Cancer / HPV Vaccine
Also Included In: Cancer / Oncology
Article Date: 03 Jun 2013 - 10:00 PDT Current ratings for:
Avastin Can Lengthen The Lives Of Advanced Cervical Cancer Patients
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The addition of targeted therapy Avastin (bevacizumab) with chemotherapy can significantly lengthen the lives of women with advanced cervical cancer by close to 30%, according to research presented at the 2013 American Society of Clinical Oncology Congress.

The finding is an important discovery in the fight against cervical cancer - the most common cancer in women under the age of 35.

More than 3,000 women in the UK are diagnosed with cervical cancer annually, while 1,000 will die from it. Cervical cancer is normally treated with surgery, radiotherapy, and chemotherapy. If the cancer is detected early and treated promptly, the prognosis is generally good.

Screening and vaccination against the human papilloma virus is crucial in preventing cervical cancer altogether, as well as keeping it from reaching an advanced stage if it does develop. For those patients who are diagnosed at an advanced stage, it becomes harder to treat the disease.

The research presented from this study is known as GOG 240. GOG 240 is an independent, National Cancer Institute (NCI) -sponsored phase III trail examining the effectiveness and safety of Avastin with chemotherapy (paclitaxel and topotecan or cisplatin) to treat women with recurrent, persistent, or advanced cervical cancer (stage IVb), that was not cured by standard treatment methods.

The study consisted of 452 women in the U.S. and Spain who were randomly assigned to one of four treatment schedules: paclitaxel and cisplatinpaclitaxel, cisplatin and Avastin (15 mg/kg every three weeks)paclitaxel and topocetan paclitaxel, topotecan and AvastinThe research revealed that the women who underwent combination treatment with chemotherapy and Avastin lived almost 30% longer, and when compared to those who were just treated with chemotherapy alone: the median overall survival was of 17 months compared to 13.3 months, respectively.

Also, the percentage of patients who responded positively to therapy increased by a third from 36% to 48%. The participants who received bevacizumab had more side effects than those who did not, however, these side effects were consistent with those previously known to be linked to bevacizumab.

Professor Stan Kaye, Head of Clinical Studies at The Institute of Cancer Research, London, and Consultant Medical Oncologist in the Gynaecology Unit at The Royal Marsden Hospital, said:

"The improvements in overall survival achieved for women with advanced cervical cancer treated with Avastin are extremely encouraging. Thousands of women are diagnosed with cervical cancer every year in the UK and for those with recurrent disease there is a desperate need for more treatment options."

Bevacizumab has a well-confirmed tolerability profile with the most frequently seen adverse effects in clinical trials listed as: hypertensionpainproteinuria (abnormal amount of protein in the bloodneutropeniaThese side effects are generally easy to take care of. The study did not find any new adverse effects. Bevacizumab was also associated with higher rates of grade 3 bleeding, thrombosis embolism, and gastrointestinal fistula.

Robert Music, Director of Jo's Cervical Cancer Trust, said:

"For women who receive a late stage diagnosis of cervical cancer the prognosis can often be poor. The results of this research look promising and if this work can go some way in improving outcomes and overall survival rates in women with advanced cervical cancer then that is a positive step."

Bevacizumab is not currently licensed for the treatment of advanced cervical cancer.

Avastin is approved for four different types of cancers in the United States: mCRC (metastatic Colorectal Cancer), NSCLC (Non-Small Cell Lung Cancer), rGBM (recurrent Glioblastoma Multiforme) and RCC (Renal Cell Cancer).

In 2011, the FDA removed the approval of Avastin for the treatment of breast cancer. The regulating body explained that Avastin is not effective or safe for that type of cancer.

Written by Kelly Fitzgerald


Copyright: Medical News Today
Not to be reproduced without permission of Medical News Today Visit our cervical cancer / hpv vaccine section for the latest news on this subject. Please use one of the following formats to cite this article in your essay, paper or report:

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5 Jun. 2013. APA

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'Avastin Can Lengthen The Lives Of Advanced Cervical Cancer Patients'

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Wednesday, June 19, 2013

A Wide Variety Of Advanced Cancers Harbor Abnormalities In HER2 Gene

Main Category: Cancer / Oncology
Also Included In: Genetics
Article Date: 04 Jun 2013 - 1:00 PDT Current ratings for:
A Wide Variety Of Advanced Cancers Harbor Abnormalities In HER2 Gene
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The HER2 growth-factor gene is known to be over-active in breast and gastro-esophageal cancers. But now, irregularities in the genes 's expression - among them mutations, amplifications, substitutions, and translocations - have been found in 14 different advanced solid tumors.

The results of the study of more than 2,000 tumors, presented at the annual meeting of the American Society of Clinical Oncology (ASCO), both surprised researchers and provided hope that some of these tumors might benefit from the three anti-HER2 therapies now in clinical use.

"No one ever thought that there would be such a variety of genomic alterations in HER2 in this many solid tumors," says Massimo Cristofanilli, MD, FACP, Professor of Medical Oncology and Director of the Jefferson Breast Center at the Kimmel Cancer Center and Thomas Jefferson University Hospital.

"But this may be good news, both clinically and scientifically," he says. "It tells us that these tumors might benefit from treatment that we already have on hand, and, from a research perspective, it builds on the idea that it is the genomic profile of a tumor that is relevant in providing biological information for planning of personalized treatments - not where the cancer is located or where it develops.'

Dr. Cristofanilli presented the results of the study in an oral presentation at the ASCO meeting. He is one of a group of co-authors from many institutions who donated tumor samples to Foundation Medicine, a cancer diagnostics company in Cambridge, Massachusetts. Foundation Medicine led and paid for the study.

Dr. Cristofanilli contributed about 50 metastatic breast tumor samples for the analysis, and found out that one of his patients with advanced triple negative breast cancer had a HER2 mutation. "My patient was treated with Herceptin as well as chemotherapy, and derived clinical benefit," he says. "No one looks for HER2 mutations in this form of breast cancer. To me, this makes the case for the value of genome-driven therapy."

In the study, Foundation Medicine conducted a genetic screen of more than 182 genes and 14 genetic rearrangements known to be linked to cancer in 2,223 tumor specimens. Twenty different advanced solid cancers were represented.

Researchers found HER2 alterations in 14 types of solid tumors, including 29 percent of esophageal, 20 percent of uterine, 14 percent of breast, 12 percent of stomach carcinomas, and 6 percent of all lung cancer samples.

They also found HER2 irregularities varied widely - 4.9 percent of specimens had 116 different HER2 alterations. That included 58 percent with amplifications, 25 percent with substitutions, 14 percent with indels (insertions/deletions of DNA), 2 percent with splice site variants, 2 percent with translocations, 5 percent with multiple alterations, and 2 tumors had both HER2 substitution and amplification.

Anti-HER2 therapies such as Herceptin can also treat HER2 mutations, and may also help block HER2 that is altered in the ways seen in the study, Dr. Cristofanilli says.

"This study highlights the need to study a broad range of genes at a high level of sensitivity and specificity when searching for novel targets of therapy," he says. "Widespread use of this approach could provide more treatment options and enable more rapid accrual to ongoing and planned trials of agents targeting pathways under study."

Article adapted by Medical News Today from original press release. Click 'references' tab above for source.
Visit our cancer / oncology section for the latest news on this subject. Dr. Cristofanilli declares no conflicts of interest related to this study.
Thomas Jefferson University Please use one of the following formats to cite this article in your essay, paper or report:

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University, Thomas Jefferson. "A Wide Variety Of Advanced Cancers Harbor Abnormalities In HER2 Gene." Medical News Today. MediLexicon, Intl., 4 Jun. 2013. Web.
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posted by John M. on 4 Jun 2013 at 11:37 am

I often think of cancer as a disease where the body doesn't attack its own tissue and autoimmune diseases as a disease where it attacks it too much. So it occurs to me that like cancer maybe some autoimmune diseases of different organs may be caused by the same underlying genetic mutation and therefore you could determine if drugs that treat one type of autoimmune disease might treat others . . .

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'A Wide Variety Of Advanced Cancers Harbor Abnormalities In HER2 Gene'

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Friday, June 14, 2013

HER2 Abnormalities Found In Many Advanced Cancers

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Main Category: Cancer / Oncology
Also Included In: Genetics
Article Date: 03 Jun 2013 - 3:00 PDT Current ratings for:
HER2 Abnormalities Found In Many Advanced Cancers
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We already know that an over-active HER2 growth factor gene features in breast and gastric cancers. Now a new study reports finding mutations and other abnormalities of the gene in 14 different advanced cancers.

Massimo Cristofanilli, Director of the Jefferson Breast Center at the Kimmel Cancer Center and Thomas Jefferson University Hospital, announced the study results at an oral presentation during the annual meeting of the American Society of Clinical Oncology (ASCO), which is taking place in Chicago until Tuesday.

The gene for human epidermal growth factor receptor 2 (HER2) codes for a protein that promotes the growth of cancer cells. In around 1 in 5 breast cancers, a mutation in the gene causes cancer cells to make too much HER2 protein. The same mutation and the higher protein levels that result, occur in many types of cancer.

But Cristofanilli's results suggest there may be several kinds of gene alteration that can have this effect: not just known mutations but also other irregularities such as amplifications, substitutions, and translocations.

Cancer is essentially a disease of failure to regulate tissue growth. It is when the genes that regulate normal cell growth become altered in some way that the cell becomes cancerous.

Every time a cell divides, the enormous amount of data contained in its genetic material is replicated. When this happens, the chances are that some errors (mutations) will occur. Cells have complex mechanisms to prevent and correct such errors. And even if the faulty cell survives, there is another process, cell suicide or apoptosis, that the body uses to deal with rogue cells.

But if all these error controls fail, then the mutations and alterations survive and are passed on to daughter cells, to sow the seeds of a tumor.

Large-scale mutations occur when a large portion of genetic material is deleted or an extra portion is added. Amplification is when a cell gains many copies of genetic material, usually containing genes known to be cancer-causing. Translocation is when two separate regions become fused.

Small-scale mutations such as point substitutions, deletions and insertions are alterations to the building block units of DNA. For instance, a substitution is a mutation that exchanges two letters of the DNA code, like changing the spelling of a word by swapping around two of its letters.

Small-scale mutations usually affect the expression of a gene and alter the function or stability of the protein it codes for.

There are also other ways genes can change to make cells cancerous, such as when viruses insert bits of their DNA into the genetic material of the host cell, causing, for example, switched off cancer genes to switch on.

In this new study, which examined more than 2,000 tumors, Cristofanilli, a professor of Medical Oncology, and colleagues, found HER2 gene irregularities in 14 different advanced solid tumors.

"No one ever thought that there would be such a variety of genomic alterations in HER2 in this many solid tumors," Cristofanilli says in a statement.

But he says the findings could be good news, "both clinically and scientifically".

It could mean Herceptin and other anti-HER2 cancer therapies that are already in clinical use might help patients with some of these tumors.

From a research point of view, the results add weight to the growing idea of "genome-driven therapy", where the genome profile of the tumor, rather than where it develops, is more important when considering how best to treat the individual patient's cancer.

A number of institutions donated tumor samples for analysis, and their researchers are co-authors of the study. Cristofanilli contributed about 50 breast cancer samples. He discovered that one sample showed one of his patients, who had been diagnosed with triple negative breast cancer, had an HER2 mutation.

"My patient was treated with Herceptin as well as chemotherapy, and derived clinical benefit," says Cristofanilli.

"No one looks for HER2 mutations in this form of breast cancer. To me, this makes the case for the value of genome-driven therapy," he explains.

Foundation Medicine, a cancer diagnostics company in Cambridge, Massachusetts led and paid for the study. They screened 2,223 solid tumor specimens from 20 different advanced cancers, for more than 182 genes alterations known to be linked to cancer.

The results showed HER2 alterations in 14 types of solid tumor. Of these, 29% were esophageal cancer samples, 20% were uterine, 14% were breast, 12% were stomach, and 6% were lung.

They also found large variations in HER2 abnormalities. They found nearly 5% of samples had 116 different abnormalities, including 58% with amplifications, 25% with substitutions, 14% with insertions or deletions, 2% with splice site variants, 2% with translocations, and 5% with more than one alteration. Plus, two of the tumors had both HER2 substitution and amplification.

Cristofanilli says the study "highlights the need to study a broad range of genes at a high level of sensitivity and specificity when searching for novel targets of therapy".

"Widespread use of this approach could provide more treatment options and enable more rapid accrual to ongoing and planned trials of agents targeting pathways under study," he adds.

Another study reported earlier this year found that while some gene alterations may actively drive tumor growth, there may also be some "passenger" alterations that do the opposite and slow cancer down, suggesting cancer may not be a sequence of inevitable accumulation of driver events, but a delicate balance between drivers and passengers.

Written by Catharine Paddock PhD


Copyright: Medical News Today
Not to be reproduced without permission of Medical News Today Visit our cancer / oncology section for the latest news on this subject. Please use one of the following formats to cite this article in your essay, paper or report:

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5 Jun. 2013. APA

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'HER2 Abnormalities Found In Many Advanced Cancers'

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Wednesday, May 29, 2013

Olaparib Active Against Advanced Ovarian Cancer and Breast Cancer with BRCA Mutations

Previously treated advanced breast and ovarian cancer patients with BRCA1 or BRCA2 gene mutation may benefit from treatment with the oral investigational drug olaparib. These findings were recently published in the journal The Lancet.[1],[2]

Although most ovarian cancer patients initially respond to platinum-based chemotherapy, most will eventually experience a return (relapse) of their cancer. Treatment of metastatic breast cancer often includes chemotherapy, but options can become limited when the cancer stops responding to conventional chemotherapy regimens. Outcomes remain poor after treatment of relapsed disease, and researchers continue to explore new approaches to treatment.

Targeted therapies are anticancer drugs that interfere with specific pathways involved in cancer cell growth or survival. Some targeted therapies block growth signals from reaching cancer cells; others reduce the blood supply to cancer cells; and still others stimulate the immune system to recognize and attack the cancer cell. Depending on the specific “target,” targeted therapies may slow cancer cell growth or increase cancer cell death.

Olaparib is an oral investigational drug called a PARP inhibitor. The PARP enzyme plays a role in DNA repair, including the repair of DNA damage from chemotherapy. Drugs that inhibit this enzyme may contribute to cancer cell death and increased sensitivity to chemotherapy.

Cancers that result from BRCA1 or BRCA2 gene mutations may be particularly responsive to PARP inhibitors. The BRCA genes provide another source of DNA repair. BRCA gene mutations result in a loss of this DNA repair capability and may make cells particularly vulnerable to the loss of other DNA repair mechanisms such as those provided by PARP.

The current Phase II studies evaluated low and high doses of olaparib in previously treated breast cancer and ovarian cancer patients with BRCA1 or BRCA2 gene mutations. Patients in both studies were treated with either 100 mg or 400 mg of oral olaparib twice a day. The studies was designed to determine overall response rate in 57 ovarian cancer patients and 54 breast cancer patients in order to validate the concept of targeting treatment for the BRCA1 or BRCA2 gene mutation, regardless of disease.

Overall response rate in the ovarian cancer study was 33% in the high-dose group and 13% in the low-dose group. Patients in the low-dose group were reported to have prognostic factors somewhat worse than the patients in the high-dose group in this study.Overall response rate in the breast cancer study was 41% in the high-dose group and 22% in the low-dose group.Side effects were tolerable in both groups.

The researchers concluded that olaparib was active in previously treated ovarian and breast cancer patients and that BRCA1 or BRCA2 mutations may play a role as a predictor for responsiveness to olaparib. Further studies are warranted to confirm these data and determine the role of BRCA mutation as a predictive biomarker that may help individualize treatment strategies for optimal results.

References:


[1] Audeh MW, Carmichael J, Penson RT, et al. Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer: a proof-of-concept trial. The Lancet [early online publication]. July 6, 2010.

[2] Tutt A, Robson M, Garber JE, et al. Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and advanced breast cancer: a proof-of-concept trial. The Lancet [early online publication]. July 6, 2010.


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Tuesday, May 28, 2013

T-DM1 Benefits Women With Advanced HER2-Positive Breast Cancer

Among women with advanced, previously treated, HER2-positive breast cancer, trastuzumab emtansine (T-DM1)-an investigational drug that combines Herceptin(r)?

(trastuzumab) and a chemotherapy drug-resulted in better progression-free survival than standard treatment. The results of this Phase III clinical trial were presented at the 2012 Annual Meeting of the American Society of Clinical Oncology.?

Approximately 20-25% of breast cancers overexpress (make too much of) the HER2 protein. HER2-targeted therapies such as Herceptin have dramatically improved outcomes for women with HER2-positive breast cancer, but researchers continue to explore new approaches to treatment.?

T-DM1 links Herceptin with a chemotherapy drug (DM1). T-DM1 delivers Herceptin and DM1 directly to HER2-positive cells, and limits exposure of the rest of the body to the chemotherapy.?

To evaluate T-DM1 for the treatment of advanced, HER2-positive breast cancer, researchers conducted a Phase III clinical trial known as EMILIA. The study enrolled close to 1000 women with locally advanced or metastatic HER2-positive breast cancer that had progressed (worsened) in spite of previous chemotherapy and Herceptin. Study participants were treated with either T-DM1 or a standard treatment. The standard treatment consisted of Xeloda(r) (capecitabine) plus?

Tykerb(r) (lapatinib). ?

*???? Survival without cancer progression was 9.6 months among women in the?

T-DM1 group and 6.4 months among women in the Xeloda and Tykerb group. ?

*???? Two-year overall survival was 65.4% among women in the T-DM1 group and?

47.5% among women in the Xeloda and Tykerb group. The survival analysis is still considered preliminary and another analysis is planned for later in the study, and will provide more definitive information about the effect of T-DM1 on overall survival.?

*???? Compared with women treated with Xeloda and Tykerb, women treated with?

T-DM1 were less likely to experience side effects such as diarrhea, hand-foot syndrome, and vomiting. The most common serious side effects of T-DM1 were low platelet counts and changes in liver function tests. ?

These results suggest that T-DM1 may be safe and effective for the treatment of advanced, previously treated, HER2-positive breast cancer. ?


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Friday, May 24, 2013

T-DM1 Produces Promising Results Against Advanced HER2-Positive Breast Cancer

Among women with metastatic, HER2-positive breast cancer, trastuzumab emtansine (T-DM1)—an investigational drug that combines HerceptinR (trastuzumab) and a chemotherapy drug—resulted in better progression-free survival than standard chemotherapy and Herceptin. The results of this Phase II clinical trial were presented at the 2011 European Multidisciplinary Cancer Congress.??

Approximately 20-25% of breast cancers overexpress (make too much of) the HER2 protein. HER2-targeted therapies such as Herceptin have dramatically improved outcomes for women with HER2-positive breast cancer, but researchers continue to explore new approaches to treatment.???

T-DM1 links Herceptin with a chemotherapy drug (DM1). T-DM1 delivers Herceptin and DM1 directly to HER2-positive cells, and limits exposure of the rest of the body to the chemotherapy.??

To evaluate T-DM1 for the initial treatment of metastatic, HER2-positive breast cancer, researchers conducted a Phase II clinical trial among 137 women. Study participants were treated with either T-DM1 or Herceptin plus TaxotereR (docetaxel).??

Survival without cancer progression was 14.2 months among women in the T-DM1 group and 9.2 months among women in the Herceptin plus Taxotere group.?In addition to delaying cancer progression, T-DM1 was also better tolerated by patients. Discontinuation of treatment due to side effects occurred in 7.2% of women in the T-DM1 group and 28.8% of women in the Herceptin plus Taxotere group.?

These results suggest that T-DM1 may be safe and effective for the treatment of advanced, HER2-positive breast cancer. Results from ongoing Phase III trials will provide additional information about this drug.?

Reference: Hurvitz S, Dirix L, Kocsis J et al. Trastuzumab emtansine (T-DM1) vs trastuzumab plus docetaxel (H+T) in previously untreated HER2-positive metastatic breast cancer (MBC): primary results of a randomized, multicenter, open-label phase II study (TDM4450g/BO21976). Presented at the 2011 European Multidisciplinary Cancer Conference. Stockholm, Sweden. September 23-27, 2011. Abstract 5001.?

Posted October 5, 2011?


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Higher Dose of Faslodex® More Effective for Advanced Breast Cancer

Among postmenopausal women with advanced, estrogen receptor-positive breast cancer that has progressed or recurred after prior hormonal therapy, a 500 mg dose of FaslodexR (fulvestrant) appears to be more effective than the originally approved 250 mg dose. These results were published in the Journal of Clinical Oncology. As a result of these findings, the 500 mg dose was recently approved by the U.S. Food and Drug Administration (FDA).

Each year roughly 200,000 U.S. women are diagnosed with breast cancer. Many of these breast cancers will be hormone receptor-positive, meaning that they are stimulated to grow by the circulating female hormones estrogen and/or progesterone. Treatment of hormone receptor-positive breast cancer often involves hormonal therapies that suppress or block the action of estrogen.

Faslodex—a type of hormonal therapy known as an estrogen receptor antagonist—blocks the actions of estrogen. It’s used for the treatment of metastatic, hormone receptor-positive breast cancer in postmenopausal women who experience cancer progression or recurrence after prior hormone therapy. Until recently, a standard dose of Faslodex was 250 mg.

In order to assess the effects of a higher dose of Faslodex, researchers conducted a Phase III clinical trial known as CONFIRM (Comparison of Faslodex in Recurrent or Metastatic breast cancer). The study compared the 250 mg dose of Faslodex to a 500 mg dose among 736 women in 17 countries.

Compared with the lower dose, the higher dose of Faslodex delayed cancer progression. Median time to cancer progression was 6.5 months among patients treated with the 500 mg dose and 5.5 months among patients treated with the 250 mg dose.After one year 34% of patients treated with the 500 mg dose were alive and free of cancer progression compared with 25% of patients treated with the 250 mg dose.No new safety concerns were identified with the 500 mg dose. The most common side effects included nausea, bone pain, back pain, and injection site pain.

The results of this study indicate that the 500 mg dose of Faslodex improves progression-free survival without increasing side effects. Based on these findings, the FDA approved the 500 mg dose for postmenopausal women with hormone receptor-positive, metastatic breast cancer that has progressed after antiestrogen therapy.

Reference: Di Leo A, Jerusalem G, Petruzelka L et al. Results of the CONFIRM Phase III trial compared fulvestrant 250 mg with fulvestrant 500 mg in postmenopausal women with estrogen receptor-positive advanced breast cancer. Journal of Clinical Oncology [early online publication]. September 20, 2010.


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Wednesday, May 22, 2013

Some Patients with Advanced Cancer Continue Screening

A significant proportion of patients with advanced cancers continue to undergo cancer screening, even though screening is unlikely to benefit these patients. These findings were recently reported in the Journal of the American Medical Association.

Cancer screening can detect disease in its early stages, before it causes symptoms. For many people, treatment at these early stages is more likely to be effective than treatment at more-advanced stages. In this way, cancer screening is credited with a substantial decline in deaths from cancer.

For people with advanced cancer, however, the benefit of screening is questionable. In such cases, screening without a known benefit may subject patients to risks of subsequent testing, biopsies, and psychological distress.

To evaluate the frequency of screening among patients with advanced cancer, researchers assessed 87,736 fee-for-service Medicare enrollees. Patients were aged 65 years or older and had been diagnosed with advanced lung, colorectal, pancreatic, grastroesophageal, or breast cancer between 1998 and 2003. These patients were matched by age, sex, and race with 87,307 Medicare enrollees who did not have cancer. Patients with cancer were followed until death or December 31, 2007, whichever came first. Screening tests evaluated included mammography, Pap test, PSA test, and lower gastrointestinal endoscopy.

Among women with an advanced cancer diagnosis, 8.9% received at least one screening mammogram compared with 22% of women without cancer.5.8% of women with advanced cancer received a Pap test compared with 12.5% of women without cancer.15% of men with an advanced cancer diagnosis received a PSA test compared with 27.2% of men without cancer.Among all patients, 1.7% with advanced diagnoses received lower gastrointestinal endoscopy compared with 4.7% of those without cancer.Patients with advanced cancer who had a recent history of screening were more likely to undergo screening following diagnosis. Other factors associated with a high probability of screening were higher socioeconomic status and being married.

The researchers conclude that even though patients with advanced cancer are unlikely to benefit from screening, many of these patients continue to undergo screening. They suggest that efforts to encourage cancer screening have resulted in such “deeply engrained habits” that patients and healthcare providers maintain screening schedules among patients with advanced cancer, for whom benefit is questionable.

Reference: Sima CS, Panageas KS, Schrag D. Cancer screening among patients with advanced cancer. JAMA.?2010;304(14):1584-1591. doi:10.1001/jama.2010.1449.


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Wednesday, May 15, 2013

Afinitor Delays Progression of Advanced Breast Cancer

Among postmenopausal women with advanced breast cancer that had become resistant to hormonal therapy, the combination of AfinitorR (everolimus) and AromasinR (exemestane) delayed cancer progression to a greater extent than Aromasin alone. The results of this Phase III clinical trial were presented at the 2011 European Multidisciplinary Cancer Congress.???

Each year roughly 200,000 U.S. women are diagnosed with breast cancer. Many of these breast cancers are hormone receptor-positive, meaning that exposure to estrogen and/or progesterone can cause them to grow.?

Treatment of hormone receptor-positive breast cancer often includes hormonal therapies such as tamoxifen or an aromatase inhibitor. Tamoxifen acts by blocking estrogen receptors, and aromatase inhibitors suppress the production of estrogen in postmenopausal women. Aromatase inhibitors include FemaraR (letrozole), ArimidexR (anastrozole), and AromasinR (exemestane). Many women with advanced breast cancer become resistant to hormonal therapy, and treatment options for these women remain limited.???

Afinitor is an oral medication that works by inhibiting a protein known as mTOR. The mTOR protein plays an important role in regulating cancer cell division and blood vessel growth.?Currently, Afinitor is used for the treatment of selected patients with kidney cancer, pancreatic neuroendocrine tumors, and subependymal giant cell astrocytoma (SEGA).??

To explore the use of Afinitor among women with advanced, estrogen receptor-positive, HER2-negative breast cancer, researchers conducted a Phase III clinical trial (BOLERO-2) among 724 women. All of the women had experienced cancer recurrence or progression in spite of treatment with Femara or Arimidex. Study participants were treated with Aromasin alone or in combination with Afinitor.???

Survival without cancer progression was 6.9 months among women treated with both Afinitor and Aromasin, compared with 2.8 months among women treated with Aromasin alone.?The most common serious side effects in the Afinitor group were stomatitis (inflammation of the lining of the mouth; 7.7%), anemia (5.8%), shortness of breath (3.9%), hyperglycemia (4.3%), fatigue (3.7%) and pneumonitis (lung inflammation; 3.1%), and elevated liver enzymes (3.1%). ?

These results suggest that the addition of Afinitor to Aromasin improved outcomes among women with advanced breast cancer that had previously been treated with hormonal therapy. Afinitor has not yet been approved for use in breast cancer.???

Reference: Baselga J, Campone M, Sahmoud T et al. Everolimus in combination with exemestane for postmenopausal women with advanced breast cancer who are refractory to letrozole or anastrozole: results of the BOLERO-2 phase III trial. Presented at the 2011 European Multidisciplinary Cancer Conference. Stockholm, Sweden. September 23-27, 2011. Abstract LBA9. ?

Posted September 30, 2011


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Tuesday, May 14, 2013

Combined HER2 Treatment Improves Outcome of Advanced Breast Cancer

Among women with metastatic, HER2-positive breast cancer, treatment with a combination of HER2-targeted therapies may produce better outcomes than treatment with only a single HER2-targeted therapy. These results were published in the New England Journal of Medicine and were also presented at the 2011 CTRC-AACR San Antonio Breast Cancer Symposium.????

Approximately 20-25% of breast cancers overexpress (make too much of) a protein known as HER2. Fortunately, the development of drugs that specifically target HER2-positive breast cancer has improved outcomes. These drugs include HerceptinR (trastuzumab), TykerbR (lapatinib), and the investigational drug pertuzumab.????

To explore whether treatment with both Herceptin and pertuzumab can improve outcomes among women with metastatic, HER2-positive breast cancer, researchers conducted a study among 808 patients. All patients received Herceptin and chemotherapy, and some patients also received pertuzumab.????

The addition of pertuzumab delayed cancer progression. Survival without cancer progression was 12.4 months among patients treated with only Herceptin and chemotherapy, and 18.5 months among patients treated with Herceptin, chemotherapy, and pertuzumab.?The addition of pertuzumab was generally well tolerated by patients, although patients in the pertuzumab group were more likely to experience febrile neutropenia (low-white blood cell count accompanied by fever) and diarrhea.?

These results suggest adding pertuzumab to Herceptin and chemotherapy may improve outcomes among women with metastatic, HER2-positive breast cancer.?

Studies are also exploring the use of pertuzumab in early-stage breast cancer.?

Reference: Baselga J, Cortes J, Kim S-B. Pertuzumab plus trastuzumab plus doxetaxel for metastatic breast cancer. New England Journal of Medicine. Early online publication December 7, 2011.?

Posted December 13, 2011?


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