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Olaparib tablet safe in pretreated ovarian cancer patients

Date:
September 10, 2014
Source:
American Association for Cancer Research
Summary:
An oral tablet form of a PARP inhibitor, olaparib, given in combination with chemotherapy, was safe in heavily pretreated ovarian cancer patients, and patients with BRCA mutations may have a better response compared with those without a BRCA mutation, according to phase Ib clinical trial data.
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An oral tablet form of a PARP inhibitor, olaparib, given in combination with chemotherapy, was safe in heavily pretreated ovarian cancer patients, and patients with BRCA mutations may have a better response compared with those without a BRCA mutation, according to phase Ib clinical trial data presented at the Marsha Rivkin Center for Ovarian Cancer Research-AACR 10th Biennial Ovarian Cancer Research Symposium, held Sept. 8-9.

"This study is one of the first studies to use olaparib tablets instead of olaparib capsules," said Saul Rivkin, MD, founder and chairman of the Marsha Rivkin Center for Ovarian Cancer Research, and a research scientist at the Swedish Cancer Institute, both in Seattle, Washington. "The goal was to find the maximum tolerated dose of olaparib tablets plus weekly metronomic carboplatin and paclitaxel in patients with relapsed ovarian cancer.

"This treatment regimen provided a response rate of 66 percent in heavily pretreated ovarian cancer patients. It was surprisingly tolerable with no grade 4 toxicities," said Rivkin.

"The outlook for ovarian cancer patients with advanced disease is not equivalent to that of breast cancer, and a lot of work needs to be done to improve the cure rate," Rivkin added. "Medical researchers are discovering and investigating new and innovative therapies for the treatment of ovarian cancer. We are constantly working toward improving the quality of life and survival for all ovarian cancer patients."

Rivkin and colleagues enrolled 14 heavily pretreated ovarian cancer patients (from three to eight prior therapies), ages 42 to 77. Patients received paclitaxel and carboplatin weekly, three weeks out of four, with increasing doses of olaparib. The maximum tolerated dose of olaparib was found to be 150 mg twice daily for three consecutive days of each week of each cycle.

Of the 12 evaluable patients, four had a complete response (33 percent), four had a partial response (33 percent), two had stable disease (16 percent), and two had disease progression (16 percent).

Three patients with a complete response, three with a partial response, one with stable disease, and one with disease progression had BRCA mutations detected in their tumors.

The most common grade 3 toxicities included neutropenia, leukopenia, lymphopenia, and anemia. There was no evidence of gastrointestinal, renal, cardiac, hepatic, pulmonary, or dermatologic toxicities in any of the patients with a toxicity grade greater than 2.

The investigators plan to recruit up to 40 additional patients in the phase II extension of this protocol.


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American Association for Cancer Research. "Olaparib tablet safe in pretreated ovarian cancer patients." ScienceDaily. ScienceDaily, 10 September 2014. <www.sciencedaily.com/releases/2014/09/140910083844.htm>.
American Association for Cancer Research. (2014, September 10). Olaparib tablet safe in pretreated ovarian cancer patients. ScienceDaily. Retrieved March 28, 2024 from www.sciencedaily.com/releases/2014/09/140910083844.htm
American Association for Cancer Research. "Olaparib tablet safe in pretreated ovarian cancer patients." ScienceDaily. www.sciencedaily.com/releases/2014/09/140910083844.htm (accessed March 28, 2024).

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