Early Use of Bevacizumab for Colorectal Cancer
Author Information
Author(s): Zafar S Yousuf, Malin Jennifer L, Grambow Steven C, Abbott David H, Schrag Deborah, Kolimaga Jane T, Zullig Leah L, Weeks Jane C, Fouad Mona N, Ayanian John Z, Wallace Robert, Kahn Katherine L, Ganz Patricia A, Catalano Paul, West Dee W, Provenzale Dawn
Primary Institution: Duke University Medical Center
Hypothesis
What is the initial dissemination pattern of bevacizumab for metastatic colorectal cancer treatment?
Conclusion
One-third of eligible metastatic colorectal cancer patients received first-line bevacizumab shortly after FDA approval.
Supporting Evidence
- 31% of patients received first-line bevacizumab in the two years after FDA approval.
- Use rose sharply within 6 months after FDA approval, then plateaued.
- Men were less likely than women to receive bevacizumab.
- Patients ≥ 75 years were less likely to receive bevacizumab than patients < 55 years.
Takeaway
This study looked at how many people with advanced colorectal cancer got a new medicine called bevacizumab after it was approved. It found that only about one in three people who could have used it actually did.
Methodology
Patient surveys and medical records were analyzed for a cohort with metastatic colorectal cancer treated in multiple regions and health systems in the US.
Potential Biases
Clinicians may have restricted their use of bevacizumab to a sub-segment of potentially eligible patients.
Limitations
The cohort is a small sub-sample drawn from a larger cohort, and longitudinal follow-up was short.
Participant Demographics
66% male, 18% aged ≥ 75 years, 62% white.
Statistical Information
P-Value
0.026
Confidence Interval
95% CI 0.32-0.93
Statistical Significance
p<0.05
Digital Object Identifier (DOI)
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