Thursday, January 26, 2012

Gene Mutations May Boost Ovarian Cancer Survival

It’s known that if you are a carrier of the BRCA1 or BRCA2 genes you have an increased chance of getting Ovarian or Breast Cancer. New research from the  Journal of the American Medical Association suggests that these genetic mutations could also have a better survival rate than those patients without the BRCA1 or BRCA2 genes.

Women with invasive epithelial ovarian cancer who carry the mutations have a better prognosis than women without the genetic variations, according to an analysis of 26 previous studies. The BRCA2 carriers, in particular, had a better five-year survival rate.

“Our paper provides definitive evidence that BRCA1 and BRCA2 carriers have improvement in survival [compared to ovarian cancer patients without the mutations],” said Kelly L. Bolton, lead author of the new analysis and a medical student at the University of California, Los Angeles, David Geffen School of Medicine.

The study, which confirms previous findings, is published Jan. 25 in the Journal of the American Medical Association. Nearly 23,000 women will get a diagnosis of ovarian cancer this year in the United States, and about 15,500 will die of it, according to the American Cancer Society. Epithelial ovarian cancer, the type Bolton focused on, occurs in the cells on the surface of the ovary. Germline BRCA1 and BRCA2 mutations are found in up to 15 percent of women with this type of cancer. A germline mutation is a gene change in a reproductive cell that can be passed on to offspring. Data from more than 1,213 ovarian cancer patients was included in the studies reviewed. Of these, 909 had BRCA1 mutations; 304 had BRCA2 variations. The studies also included 2,666 women who did not have the genetic mutations. At the five-year mark, 44 percent of the BRCA1 carriers and 52 percent of the BRCA2 carriers were alive, compared to 36 percent of those without the mutation.

Bolton said the survival differences remained after the researchers took into account such factors as the stage of the cancer and age, although it was less significant among women with a family history of ovarian and/or breast cancer. Exactly how the mutations may improve survival is not known. However, Bolton and others speculate the BRCA1 or BRCA2 status may modify the response to platinum-based chemotherapy, a common treatment. The new analysis will have important implications for future research and treatment of ovarian cancer, the authors said. Routine genetic screening of women with high-grade cancer might be warranted, they added.

Dr. Elizabeth Poynor, a gynecologic oncologist and pelvic surgeon at Lenox Hill Hospital in New York City, suggested the findings can help health care providers tailor treatment and more accurately counsel them regarding expected survival. While not new, the information is valuable, Poynor said. “For a long time, we’ve known that individuals with BRCA1 or 2 actually have a better prognosis,” she said. “This is not new information, it’s expanded information. It’s reinforcing what we already know.”

Read more: http://news.health.com/2012/01/24/gene-mutations-may-boost-ovarian-cancer-survival-study/

Wednesday, January 18, 2012

“BEAT” Ovarian Cancer by Recognizing the Signs

“BEAT” this disease by recognizing the signs:
Bloating that is persistent
Eating less and feeling fuller
Abdominal pain
Trouble with your bladder

If any symptoms continue for 2-3 weeks, it's very important to tell your doctor! Please remember that Ovarian Cancer is the deadliest gynecologic cancer and the earlier that it’s caught, the better off you’ll be.

Monday, January 9, 2012

Texas Hold 'Em Poker Tournament will be Hosted by Pittsburgh Penguins Alumni on Thursday to benefit Breast Cancer Research

Time: 5:00 pm - 1:00 am

Cost: $220 entry fee

Location: The Rivers Casino, Pittsburgh, PA

The Pittsburgh Penguins Alumni Association will host its first-ever Texas Hold 'Em Poker Tournament at The Rivers Casino in Pittsburgh on Thursday, January 12 to benefit breast cancer research and awareness at Magee-Women’s Research Institute & Foundation, the Mario Lemieux Foundation, and the Alumni’s Scholarship Fund.

The tournament will begin at 5:00 pm and the championship game is expected to conclude by 1:00 am.

Reservations are now available for a $220 entry fee. A Penguins alumnus will host each table for the first round of play.

To make a reservation, click here. All participants must be 21 years or older to be on The Rivers Casino property. In addition, a valid driver’s license is required for all participants.

Wednesday, January 4, 2012

New Hybrid Imaging Device Shows Promise in Spotting Hard-To-Detect Ovarian Cancer

Promising new technology from the University of Connecticut and the University of Southern California.

By combining three previously unrelated imaging tools into one new device, a team of researchers from the University of Connecticut and the University of Southern California has proposed a new way to diagnose early-stage ovarian cancer in high-risk women through minimally invasive surgery. The new technique may be better than the current standard procedure of preemptively removing the ovaries.

Ovarian cancer has a low survival rate because a lack of reliable screening techniques usually means the disease remains hidden until the later stages. Now researchers have drawn on the unique advantages of multiple imaging tools to test a new way of spotting early-on the tissue irregularities that signal cancer.

For their diagnostic device, the researchers combined the contrast provided by photoacoustic imaging, the high-resolution subsurface imaging provided by optical coherence tomography, and the deeper tissue imaging provided by pulse-echo ultrasound. They tested their device, described by the team in the September issue of the Optical Society's (OSA) open-access journal Biomedical Optics Express, by imaging both pig and human ovarian tissue, and correctly identified malignant tumors that were later confirmed by staining the tissue and examining it under a microscope. These initial tests were performed on tissue that had been surgically removed, but the diameter of the device -- at only 5 mm -- is small enough that it could potentially be inserted through a small slit to image tissue in live patients.

Read more: http://www.sciencedaily.com/releases/2011/09/110913103115.htm

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