Cancer Drug Used in Combination with Other Therapies Associated With Increased Risk of Death
CHICAGO, Feb. 1, 2011—An analysis of previous studies indicates that compared with chemotherapy alone, use of the cancer drug bevacizumab in combination with chemotherapy or biological therapy is associated with an increased risk of treatment-related death, according to an article in the February 2 issue of JAMA.
A fatal adverse event (FAE) is defined as a death caused in all likelihood by a drug and is a major cause of fatality in the United States. Bevacizumab was approved in combination with chemotherapy for treating many types of advanced cancer, including colorectal cancer, non-small cell lung cancer, breast cancer, and renal cell carcinoma. "Even though a number of FAEs have been reported in patients treated with bevacizumab, its role in the development of these fatal events has not been definitively established. Data across bevacizumab trials reveal conflicting results regarding its associations with FAEs," according to background information in the article.
Vishal Ranpura, M.D., of Stony Brook University Medical Center, Stony Brook, N.Y., and colleagues conducted a review and meta-analysis of published randomized controlled trials (RCTs) to determine whether bevacizumab is associated with increased rates of FAEs in patients with cancer. The researchers identified and included 16 RCTs in the analysis. These RCTs included a total of 10,217 patients with a variety of advanced solid tumors. Eligible studies included RCTs in which bevacizumab in combination with chemotherapy or biological therapy was compared with chemotherapy or biological therapy alone.
The overall incidence of FAEs with bevacizumab was 2.5 percent. Compared with chemotherapy alone, the addition of bevacizumab was associated with a 1.5 times increased risk of FAEs. This association varied significantly with chemotherapeutic agents but not with tumor types or bevacizumab doses. Bevacizumab was associated with a 3.5 times increased risk of FAEs in patients receiving taxanes or platinum agents (3.3 percent vs. 1.0 percent), but was not associated with increased risk of FAEs when used in conjunction with other agents.
Common specific causes of FAEs included hemorrhage (23.5 percent), neutropenia (a blood disorder; 12.2 percent), gastrointestinal tract perforation (7.1 percent), pulmonary embolism (5.1 percent), and cerebrovascular accident (5.1 percent). Pulmonary (14/23) and gastrointestinal hemorrhage (6/23) accounted for most fatal bleeding events.
The authors write that given the absolute risk of
treatment-related mortality appears low, the use of bevacizumab
should be considered in the context of overall survival benefits.
They add that because bevacizumab is increasingly used in cancer
patients, it is particularly important for all health care
practitioners and patients to understand and recognize the risk of
treatment-related mortality and to monitor closely to identify and
treat serious adverse effects.
(JAMA 2011;305:487-494. Available pre-embargo to the media at www.jamamedia.org)
Editor's Note: Please see the article for additional information, including other authors, author contributions and affiliations, financial disclosures, funding and support, etc.
Editorial: Bevacizumab Treatment for Solid Tumors
In an accompanying editorial, Daniel F. Hayes, M.D., of the University of Michigan Comprehensive Cancer Center, Ann Arbor, Mich., writes that careful review of response rates to bevacizumab suggest that bevacizumab works well, but only in selected patients.
"Is bevacizumab a boon or a bust? The jury is still out.
Although bevacizumab has benefit, it is currently not possible to
determine in whom or for how long. Thus, oncologists are forced to
dilute the potential effects of bevacizumab by exposing all treated
patients, and society, to enormous costs and occasional
life-threatening toxic effects. These unfortunate circumstances are
sad for those who pay the bills—and sadder for patients with
(JAMA 2011;305:506-508. Available pre-embargo to the media at www.jamamedia.org)
Editor's Note: Please see the article for additional information, including financial disclosures, funding and support, etc.
For more information, contact JAMA/Archives media relations at 312/464-JAMA (5262) or e-mail firstname.lastname@example.org.
Media Advisory: To contact corresponding author Shenhong Wu, M.D., Ph.D., call Greg Filiano at 631-444-9343 or email email@example.com. To contact editorial author Daniel F. Hayes, M.D., call Nicole Fawcett at 734-764-2220 or email firstname.lastname@example.org.
Posted: February 2011
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