Impact of Subsequent Therapies on Outcome of the FIRE-3/AIO KRK0306 Trial: First-Line Therapy With FOLFIRI Plus Cetuximab or Bevacizumab in Patients With KRAS Wild-Type Tumors in Metastatic Colorectal Cancer
- PMID: 26261259
- DOI: 10.1200/JCO.2015.61.2887
Impact of Subsequent Therapies on Outcome of the FIRE-3/AIO KRK0306 Trial: First-Line Therapy With FOLFIRI Plus Cetuximab or Bevacizumab in Patients With KRAS Wild-Type Tumors in Metastatic Colorectal Cancer
Abstract
Purpose: We investigated choice and efficacy of subsequent treatment, with special focus on second-line therapy, in the FIRE-3 trial (FOLFIRI plus cetuximab [arm A] or bevacizumab [arm B]) for patients with KRAS wild-type metastatic colorectal cancer.
Patients and methods: Start of subsequent-line (second or third) therapy was defined as use of an antitumor drug that was not part of the previous regimen. We evaluated choice, duration, and efficacy of subsequent therapy and determined the impact of subsequent-line treatment on outcome of patients in FIRE-3.
Results: Of 592 patients in the intent-to-treat population, 414 (69.9%) received second-line and 256 (43.2%) received third-line therapy. In subsequent treatment lines, 47.1% of patients originally assigned to arm A received bevacizumab, and 52.2% originally assigned to arm B received either cetuximab or panitumumab. Oxaliplatin was subsequently used in 55.9% (arm A) and 53.2% (arm B) of patients. Second-line therapy was administered for a median duration of 5.0 versus 3.2 months (P < .001) in study arm A versus B. Progression-free (6.5 v 4.7 months; hazard ratio, 0.68; 95% CI, 0.54 to 0.85; P < .001) and overall survival (16.3 v 13.2 months; hazard ratio, 0.70; 95% CI, 0.55 to 0.88; P = .0021) from start of second-line therapy were longer in patients in arm A compared with arm B.
Conclusion: Our data suggest that the sequence of drug application might be more important than exposure to single agents. In patients with RAS wild-type tumors, first-line application of anti-epidermal growth factor receptor-directed therapy may represent a favorable condition for promoting effective subsequent therapy including antiangiogenic agents.
Trial registration: ClinicalTrials.gov NCT00433927.
© 2015 by American Society of Clinical Oncology.
Comment in
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Trying to Understand Differing Results of FIRE-3 and 80405: Does the First Treatment Matter More Than Others?J Clin Oncol. 2015 Nov 10;33(32):3686-8. doi: 10.1200/JCO.2015.62.8495. Epub 2015 Aug 31. J Clin Oncol. 2015. PMID: 26324365 No abstract available.
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Reply to G. Nasti and A. Ottaiano and to A. Avallone and A. Budillon.J Clin Oncol. 2016 May 1;34(13):1565-6. doi: 10.1200/JCO.2015.66.3799. Epub 2016 Mar 7. J Clin Oncol. 2016. PMID: 26951313 No abstract available.
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Best Sequence Therapy in RAS Wild-Type Metastatic Colorectal Cancer: Waiting for Randomized Crossover Clinical Trials.J Clin Oncol. 2016 May 1;34(13):1563-4. doi: 10.1200/JCO.2015.65.9086. Epub 2016 Mar 7. J Clin Oncol. 2016. PMID: 26951319 No abstract available.
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Impact of Subsequent Therapies on Outcome of the FIRE-3/AIO KRK0306 Trial.J Clin Oncol. 2016 May 1;34(13):1564. doi: 10.1200/JCO.2015.66.1512. Epub 2016 Mar 7. J Clin Oncol. 2016. PMID: 26951321 No abstract available.
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