We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
INTEGRA BIOSCIENCES AG

Download Mobile App




Cell-Based Assay Determines Ideal Treatment for Ovarian Cancer

By Labmedica staff writers
Posted on 27 May 2008
A cell-based assay examines the response of a specific patient's tumor to various chemotherapies, and correlates with significantly longer overall survival (OS) in patients with primary ovarian cancer.

The assay, called ChemoFx, is a decision support tool that measures a patient's tumor response to various types, combinations, and doses of chemotherapy selected by the patient's physician. More...
The laboratory test examines how many cancer cells are killed after exposure to treatment, using the patient's living cancer cells that have been removed during a biopsy, aspiration, or surgical procedure. ChemoFx can be used in primary, recurrent, and metastatic tumors.

Other solid tumors most commonly tested include endometrial, colorectal, genitourinary, head and neck, lung, brain, pancreas, and hepatobiliary. Patients who received a treatment determined by ChemoFx to lead to the best tumor response had an overall survival 1.4 times longer than those receiving a treatment shown by ChemoFx to be non-responsive.

In a study lead by Thomas J. Herzog, M.D., director of gynecologic oncology at the Columbia University Medical Center (New York, NY, USA), it was found that although patients had the same type of tumor, 88% exhibited varying degrees of response to different agents when evaluated by the cell-based test. The analysis also found that nearly two-thirds of patients' tumors were more responsive to a treatment identified by ChemoFx, than to the treatment they actually received. Based on these results, a mathematical model was created to estimate survival, had patients been treated with a drug that ChemoFx identified as more likely to result in a greater tumor response. The analysis found that median OS could be extended as much as 23 to 38 months.

"These overall survival data demonstrate that the responsiveness to treatment established by this sensitivity assay in the laboratory setting, may in fact translate into meaningful clinical outcomes for patients,” said Dr. Herzog. "If these results are confirmed in current ongoing trials, this will be a significant step towards establishing individualized treatment strategies for patients who will require chemotherapy.”

ChemoFx is a product of Precision Therapeutics (Pittsburg, PA, USA), an oncology services company dedicated to the individualization of cancer therapy.

This retrospective, multi-center analysis was a published abstract at the American Society of Clinical Oncology (ASCO) annual meeting in (Chicago; IL, USA), which took place from May 30-June 3, 2008.


Related Links:
Columbia University Medical Center
Precision Therapeutics

New
Gold Member
Automatic Hematology Analyzer
CF9600
POC Helicobacter Pylori Test Kit
Hepy Urease Test
New
Japanese Encephalitis Test
Japanese Encephalitis Virus Real Time PCR Kit
New
Steam Sterilizer
Hi Vac II Line
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Immunology

view channel
Image: Accurate immunotherapy selection for esophageal and GEJ carcinomas depends on consistent PD-L1 assessment (credit: Adobe Stock)

FDA Approval Expands Use of PD-L1 Companion Diagnostic in Esophageal and GEJ Carcinomas

Esophageal and gastroesophageal junction carcinomas (GEJ) have a poor prognosis, with approximately 16,250 deaths in the United States in 2025 and a five-year relative survival of 21.9%.... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.