Clinical Trials for Ovarian Cancer Patients: Why Now?

February 1, 2013 7:44 pm

The following article is provided by The Clearity Foundation to support women with ovarian cancer and their families. Learn more about The Clearity Foundation and the services we provide directly to women as they make treatment decisions and navigate emotional impacts of their diagnosis.

Clinical Trials for Ovarian Cancer Patients: Why Now?

By: Cory Bentley, PhD & Teresa Gallagher, PhD

Ovarian cancer is a very diverse disease on the molecular level. Different tumors have different key molecular players and potentially different Achilles’ heels. Researchers are making real progress in pinpointing key players involved in this disease, spurring the movement of new drugs into the clinic that target these newly identified players.  For example, a 2011 study by The Cancer Genome Atlas (TCGA) research consortium found that ~35% of ovarian cancers have alterations in a molecular pathway known as PI3K/AKT. This pathway is important in cancer cell growth. New drugs targeting this pathway have entered clinic trials for ovarian cancer patients (e.g. MK-2206, which targets AKT and BYL719, which targets PI3K).

“This is cutting edge science,” says Dr. Evan Friend, who volunteers with Clearity to evaluate clinical trial data. Dr. Friend points out that if an ovarian cancer patient’s tumor suggests that her cancer may be responsive to a clinical trial drug, it gives her more treatment options that may lead to remission. “Although these drugs are new, there is a foundation of research supporting their clinical evaluation.” Drugs that progress into clinical trials have already been thoroughly evaluated and tested in the laboratory and in animal models. By considering clinical trial drugs in addition to already approved drugs, more opportunities open for ovarian cancer patients to tailor their treatments to match their molecular profiles. This approach of matching treatment options to the patient’s molecular profile defines personalized medicine.

Continuing progress in understanding molecular drivers in cancer, combined with significant technological advances in evaluating the associated molecular profiles, provide new opportunities for ovarian cancer patients to personalize their treatments. Foundation Medicine is leveraging these cutting edge advancements, so-called next-generation sequencing, to perform genomic analysis to detect alterations in relevant cancer genes. While Clearity’s standard profile is focused on markers relevant to approved drugs, the genomic information that is obtained by sequencing a more expansive set of genes may have implications for drugs in clinical trials. Ovarian cancer molecular profiling from both panels provides the most comprehensive molecular profile available for ovarian cancer patients to date. The  best-tailored fit may be from already approved drugs or may be from drugs just now making their way through clinical trials or from a combination chemotherapy-clinical trial drug based on the individual tumor profile.

There are currently 235 ongoing clinical trials for ovarian cancer in the United States. Approximately 25% of these are testing drugs that target specific proteins and pathways that have been shown to be active in pre-clinical ovarian cancer models.  More drugs will continue to enter clinical trials, increasing the opportunities and options for ovarian cancer patients.

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