Bevacizumab beyond first progression is associated with prolonged overall survival in metastatic colorectal cancer: results from a large observational cohort study (BRiTE) - PubMed (original) (raw)
Multicenter Study
. 2008 Nov 20;26(33):5326-34.
doi: 10.1200/JCO.2008.16.3212. Epub 2008 Oct 14.
Affiliations
- PMID: 18854571
- DOI: 10.1200/JCO.2008.16.3212
Multicenter Study
Bevacizumab beyond first progression is associated with prolonged overall survival in metastatic colorectal cancer: results from a large observational cohort study (BRiTE)
Axel Grothey et al. J Clin Oncol. 2008.
Abstract
Purpose: Bevacizumab provides a survival benefit in first- and second-line metastatic colorectal cancer (mCRC). In a large, observational, bevacizumab treatment study (Bevacizumab Regimens: Investigation of Treatment Effects and Safety [BRiTE]) in patients who had mCRC, a longer-than-expected overall survival (OS) of 25.1 months was reported. The association between various pre- and post-treatment factors (including the use of bevacizumab beyond first progression [BBP]) and survival was examined.
Patients and methods: The 1,445 of 1,953 previously untreated patients with mCRC who were enrolled in BRiTE and who experienced disease progression (PD) were classified into three groups: no post-PD treatment (n = 253), post-PD treatment without bevacizumab (no BBP; n = 531), and BBP (n = 642). Relevant baseline and on-study variables, including BBP, were analyzed with a Cox model with respect to their independent effect on survival beyond first PD.
Results: Median OS was 25.1 months (95% CI, 23.4 to 27.5 months), and median progression-free survival was 10.0 months in the overall BRiTE population. Baseline and postbaseline factors were well balanced between the BBP and no-BBP groups. Median OS rates were 12.6, 19.9, and 31.8 months in the no post-PD treatment, no-BBP, and BBP groups, respectively. In multivariate analyses, compared with no BBP, BBP was strongly and independently associated with improved survival (HR, 0.48; P < .001). Hypertension that required medication was the only bevacizumab-related safety event that occurred more frequently in the BBP group (24.6% v 19.2%).
Conclusion: These results from a large, prospective, observational study suggest that continued vascular endothelial growth factor inhibition with bevacizumab beyond initial PD could play an important role improving the overall success of therapy for patients who have mCRC.
Comment in
- Bevacizumab beyond progression: does this make sense?
Ellis LM, Haller DG. Ellis LM, et al. J Clin Oncol. 2008 Nov 20;26(33):5313-5. doi: 10.1200/JCO.2008.17.4540. Epub 2008 Oct 14. J Clin Oncol. 2008. PMID: 18854567 No abstract available. - Hidden biases in an observational study of bevacizumab beyond progression.
Kopetz S, Abbruzzese JL. Kopetz S, et al. J Clin Oncol. 2009 Apr 1;27(10):1732-3; author reply 1733. doi: 10.1200/JCO.2009.21.2084. Epub 2009 Mar 2. J Clin Oncol. 2009. PMID: 19255299 No abstract available. - Targeted therapies: Goldie-Coldman and bevacizumab beyond disease progression.
Giantonio BJ. Giantonio BJ. Nat Rev Clin Oncol. 2009 Jun;6(6):311-2. doi: 10.1038/nrclinonc.2009.66. Nat Rev Clin Oncol. 2009. PMID: 19483736
Similar articles
- Clinical outcomes associated with bevacizumab-containing treatment of metastatic colorectal cancer: the BRiTE observational cohort study.
Kozloff M, Yood MU, Berlin J, Flynn PJ, Kabbinavar FF, Purdie DM, Ashby MA, Dong W, Sugrue MM, Grothey A; Investigators of the BRiTE study. Kozloff M, et al. Oncologist. 2009 Sep;14(9):862-70. doi: 10.1634/theoncologist.2009-0071. Epub 2009 Sep 2. Oncologist. 2009. PMID: 19726453 - Bevacizumab exposure beyond first disease progression in patients with metastatic colorectal cancer: analyses of the ARIES observational cohort study.
Grothey A, Flick ED, Cohn AL, Bekaii-Saab TS, Bendell JC, Kozloff M, Roach N, Mun Y, Fish S, Hurwitz HI. Grothey A, et al. Pharmacoepidemiol Drug Saf. 2014 Jul;23(7):726-34. doi: 10.1002/pds.3633. Epub 2014 May 16. Pharmacoepidemiol Drug Saf. 2014. PMID: 24830357 - Phase II trial of chemotherapy plus bevacizumab as second-line therapy for patients with metastatic colorectal cancer that progressed on bevacizumab with chemotherapy: the Gunma Clinical Oncology Group (GCOG) trial 001 SILK study.
Tsutsumi S, Ishibashi K, Uchida N, Ojima H, Hosouchi Y, Yashuda N, Kigure W, Yamauchi S, Asao T, Ishida H, Kuwano H. Tsutsumi S, et al. Oncology. 2012;83(3):151-7. doi: 10.1159/000337992. Epub 2012 Aug 7. Oncology. 2012. PMID: 22889925 Clinical Trial. - Bevacizumab in the treatment of metastatic colorectal cancer (mCRC) in second- and third-line settings.
Giantonio BJ. Giantonio BJ. Semin Oncol. 2006 Oct;33(5 Suppl 10):S15-8. doi: 10.1053/j.seminoncol.2006.08.003. Semin Oncol. 2006. PMID: 17145520 Review. - Bevacizumab: an angiogenesis inhibitor for the treatment of solid malignancies.
Shih T, Lindley C. Shih T, et al. Clin Ther. 2006 Nov;28(11):1779-802. doi: 10.1016/j.clinthera.2006.11.015. Clin Ther. 2006. PMID: 17212999 Review.
Cited by
- Efficacy and safety of PD-1/L1 inhibitors as first-line therapy for metastatic colorectal cancer: a meta-analysis.
Huang Z, Li C, Huang Y, Liang W, Tao H. Huang Z, et al. Front Immunol. 2024 Jul 19;15:1425596. doi: 10.3389/fimmu.2024.1425596. eCollection 2024. Front Immunol. 2024. PMID: 39100666 Free PMC article. - Impact of bevacizumab on clinical outcomes and its comparison with standard chemotherapy in metastatic colorectal cancer patients: a systematic review and meta-analysis.
Naz T, Rehman AU, Shahzad A, Rasool MF, Saleem Z, Hussain R. Naz T, et al. J Pharm Policy Pract. 2024 Jun 5;17(1):2354300. doi: 10.1080/20523211.2024.2354300. eCollection 2024. J Pharm Policy Pract. 2024. PMID: 38845624 Free PMC article. - Cetuximab Treatment beyond Progression in Patients with Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma: A Nationwide Population-Based Study (THNS-2021-08).
Wang HM, Lou PJ, Yang MH, Chen TH, Lien MY, Lin JC, Chen JP, Lu WC, Lu HJ, Huang TL, Yen CJ, Wu SY, Wang HC, Hsieh MC. Wang HM, et al. Target Oncol. 2024 Jan;19(1):51-58. doi: 10.1007/s11523-023-01028-7. Epub 2024 Jan 29. Target Oncol. 2024. PMID: 38285067 Free PMC article. - Overall survival of patients with hepatocellular carcinoma treated with sintilimab and disease outcome after treatment discontinuation.
Wang K, Xiang YJ, Yu HM, Cheng YQ, Feng JK, Liu ZH, Shan YF, Zheng YT, Ni QZ, Cheng SQ. Wang K, et al. BMC Cancer. 2023 Oct 23;23(1):1017. doi: 10.1186/s12885-023-11485-y. BMC Cancer. 2023. PMID: 37867191 Free PMC article. - Current Status of Angiogenesis Inhibitors as Second-Line Treatment for Unresectable Colorectal Cancer.
Otsu S, Hironaka S. Otsu S, et al. Cancers (Basel). 2023 Sep 14;15(18):4564. doi: 10.3390/cancers15184564. Cancers (Basel). 2023. PMID: 37760533 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical