Phase III Study Comparing Gemcitabine Plus Cetuximab Versus Gemcitabine in Patients With Advanced Pancreatic Adenocarcinoma: Southwest Oncology Group–Directed Intergroup Trial S0205
Southeast Clinical Oncology Research Consortium
Abstract
A total of 745 eligible patients were accrued. No significant difference was seen between the two arms of the study with respect to the median survival time (6.3 months for the gemcitabine plus cetuximab arm v 5.9 months for the gemcitabine alone arm; hazard ratio = 1.06; 95% CI, 0.91 to 1.23; P = .23, one-sided). Objective responses and progression-free survival were similar in both arms of the study. Although time to treatment failure was longer in patients on gemcitabine plus cetuximab (P = .006), the difference in length of treatment was only 2 weeks longer in the combination arm. Among patients who were studied for tumoral EGFR expression, 90% were positive, with no treatment benefit detected in this patient subset.
In patients with advanced pancreas cancer, the anti-EGFR monoclonal antibody cetuximab did not improve the outcome compared with patients treated with gemcitabine alone. Alternate targets other than EGFR should be evaluated for new drug development.
Citation impact
- FWCI
- 28.50
- Percentile
- 100%
- References
- 16
Authors
15- PAPhilip A. PhilipCorresponding
Southeast Clinical Oncology Research Consortium
- JBJacqueline Benedetti
Southeast Clinical Oncology Research Consortium
- CLChristopher L. Corless
Southeast Clinical Oncology Research Consortium
- RWRalph Wong
Southeast Clinical Oncology Research Consortium
- EMEileen M. O’Reilly
Southeast Clinical Oncology Research Consortium
Topics & keywords
- Cetuximab
- Gemcitabine
- Medicine
- Oncology
- Internal medicine
- Pancreatic cancer
- Clinical endpoint
- Hazard ratio
- Good health and well-being