Treatment Patterns and Clinical Outcomes in Patients With Metastatic Colorectal Cancer Initially Treated with FOLFOX–Bevacizumab or FOLFIRI–Bevacizumab: Results From ARIES, a Bevacizumab Observational Cohort Study

Author:

Bendell Johanna C.1,Bekaii-Saab Tanios S.2,Cohn Allen L.3,Hurwitz Herbert I.4,Kozloff Mark5,Tezcan Haluk6,Roach Nancy7,Mun Yong8,Fish Susan8,Flick E. Dawn8,Dalal Darshan8,Grothey Axel9

Affiliation:

1. a Sarah Cannon Research Institute, Nashville, Tennessee, USA;

2. b The Ohio State University Medical Center, Columbus, Ohio, USA;

3. c Rocky Mountain Cancer Center, Denver, Colorado, USA;

4. d Duke University Medical Center, Durham, North Carolina, USA;

5. e Ingalls Hospital and University of Chicago, Harvey, Illinois, USA;

6. f Kootenai Cancer Center, Coeur d'Alene, Idaho, USA;

7. g FightColorectalCancer.org, Patient Advocacy, Alexandria, Virginia, USA;

8. h Genentech, Inc., South San Francisco, California, USA;

9. i Mayo Clinic College of Medicine, Rochester, Minnesota, USA

Abstract

Abstract Background. The Avastin® Registry: Investigation of Effectiveness and Safety (ARIES) study is a prospective, community-based observational cohort study that evaluated the effectiveness and safety of first-line treatment patterns, assessing the impact of chemotherapy choice and treatment duration. Methods. The ARIES study enrolled patients with metastatic colorectal cancer (mCRC) receiving first-line chemotherapy with bevacizumab and followed them longitudinally. The protocol did not specify treatment regimens or assessments. Analyses included all patients who initiated bevacizumab in combination with either first-line oxaliplatin with infusional 5-fluorouracil and leucovorin (FOLFOX) or irinotecan with infusional 5-fluorouracil and leucovorin (FOLFIRI). Progression-free survival (PFS) and overall survival (OS) times were estimated using Kaplan–Meier methods. Hazard ratios (HRs) were estimated with multivariate Cox regression analysis, adjusting for potential confounding factors. Results. In total, 1,550 patients with first-line mCRC were enrolled (median follow-up, 21 months) and most received FOLFOX–bevacizumab (n = 968) or FOLFIRI–bevacizumab (n = 243) as first-line therapy. The baseline characteristics and median treatment duration were generally similar between subgroups. There were no significant differences in the median PFS (10.3 months vs. 10.2 months) or OS (23.7 months vs. 25.5 months) time between the FOLFOX–bevacizumab and FOLFIRI–bevacizumab subgroups, respectively, by unadjusted analyses. Multivariate analyses showed FOLFIRI–bevacizumab resulted in a similar PFS (HR, 1.03; 95% confidence interval [CI], 0.88–1.21) and OS (HR, 0.95; 95% CI, 0.78–1.16) outcome as with FOLFOX–bevacizumab. The incidence proportions of bevacizumab-associated adverse events were similar for FOLFOX- and FOLFIRI-based therapies. Conclusions. In first-line mCRC patients, the FOLFOX–bevacizumab and FOLFIRI–bevacizumab regimens were associated with similar treatment patterns and clinical outcomes.

Funder

Genentech, Inc.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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