Tarceva-Avastin Combination Doesn’t Prolong Lung Cancer Survival

By Alice Carver
14:00, October 7th 2008
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Tarceva-Avastin Combination Doesn’t Prolong Lung Cancer Survival

According to the results of a late-stage clinical trial into the benefits of combining Genentech’s cancer drug Avastin (bevacizumab) to the drug Tarceva (erlotinib), the combined treatment didn’t prolong the lives of patients with advanced lung cancer. The results of the study were recently published in a press release by Genentech.

Roche Holding, the world’s larger maker of cancer drugs, and Genentech Inc said on Monday a Phase III study investigated the addition of Avastin to Tarceva compared with Tarceva alone for the treatment of patients with advanced non-small cell lung cancer, the most prevalent form of the disease. Genentech, based in South San Francisco, Calif. Co-markets Tarceva with OSI Pharmaceuticals, Melville, N.Y., which developed Tarceva; Roche Holding AG sells both drugs in Europe. Roche wants to buy Genentech, which is already majority-owned by Roche. The company offered $89 a share this summer to buy the Genentech outright. But the company’s board rejected the offer as too low.  

Tarceva and Avastin are on the market for treating lung cancer. Tarceva is used to treat pancreatic cancer and Avastin is approved to treat colorectal and breast cancers.  

The study did not show an improvement in overall survival with the Avastin-Tarceva combination compared with Tarceva alone. However, the combination treatment showed clear evidence of clinical activity, with improvements in progression-free survival (PFS) and response rate. Adverse events were consistent with those observed in previous NSCLC clinical trials evaluating the agents.

“We are disappointed this study didn’t show an improvement in survival for patients with advanced lung cancer who have a poor prognosis and a disease that is extremely difficult to treat,” Hal Barron, Genentech’s chief medical officer, said in a prepared statement Monday.

“We are, however, encouraged to see the combination of Avastin and Tarceva had clear evidence of biological activity, and will fully analyse the data so that we can apply the insights to our ongoing lung cancer research.”

The companies are further analyzing the study results and will submit the data for presentation at the 2008 Chicago Multidisciplinary Symposium in Thoracic Oncology in Chicago, Ill., November 13-15.

Lung cancer is the leading cause of cancer-related deaths in the United States and Europe and is responsible for nearly 30 percent of cancer deaths among men and women in the United States. Advanced non–small cell lung cancer (NSCLC) is the most common type of lung cancer. Current treatments are aimed to destroy tumor cells or prevent further tumor growth.

Avastin is based on anti-angiogenesis mechanism, designed to combat cancer by preventing the formation of blood vessels that supply tumours. The drug simply inteferes with the blood supply of a tumor, cutting its ability to grow and spread in the body. Studies show the drug slows tumor growth, without increasing lifespan. The drug is being tested for more widespread use in cancer during a debate focusing on the balance between its benefits and its price. The medication can cost up to $100,000 per year and, although that expensive, the drug may only help people live longer by just a few months.

Despite the fact that Avastin proved efficient in slowing the development of breast cancer, patients taking Avastin did not live for too long. Studies showed that Avastin combined with chemotherapy was successful in treating breast cancer, lengthening the time before the cancer worsened. Avastin also has serious side effects, such as bleeding, heart attack or stroke.

A second study (ATLAS) is evaluating the combination of Avastin and Tarceva as a potential first-line maintenance therapy for advanced non-small cell lung cancer patients whose disease has not progressed following initial treatment with Avastin in combination with chemotherapy. Results are expected in the first half of 2009.



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