Adverse Events Associated With Bevacizumab and Chemotherapy in Older Patients With Metastatic Colorectal Cancer

被引:9
作者
Shankaran, Veena [1 ,2 ,3 ]
Mummy, David [1 ]
Koepl, Lisel [1 ]
Blough, David [2 ,3 ]
Yim, Yeun Mi [4 ]
Yu, Elaine [4 ]
Ramsey, Scott [1 ,2 ,3 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA
[2] Univ Washington, Sch Med, Seattle, WA 98109 USA
[3] Univ Washington, Sch Pharm, Pharmaceut Outcomes Res & Policy Program, Seattle, WA 98109 USA
[4] Genentech Inc, San Francisco, CA 94080 USA
关键词
First-line; Incidence of adverse events; Preexisting conditions; Safety; SEER-Medicare; SEER-MEDICARE DATA; RECEIVING BEVACIZUMAB; ELDERLY-PATIENTS; CLAIMS DATA; OXALIPLATIN; FLUOROURACIL; COMBINATION; POPULATION; REGIMENS; EFFICACY;
D O I
10.1016/j.clcc.2012.11.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The safety of bevacizumab in older metastatic colorectal cancer (mCRC) patients is not well characterized. A total of 6821 mCRC patients age >= 65 were identified from Surveillance, Epidemiology and End Results Program (SEER)-Medicare and were categorized by first-line treatment (none, chemotherapy alone, chemotherapy and bevacizumab). First-line bevacizumab was not associated with increased adverse event (AE) incidence or first AE risk compared with chemotherapy alone, when controlling for potential confounders. Background: The safety of bevacizumab in older mCRC patients is poorly understood. The purpose of this analysis was to determine the prevalence, incidence, and risk factors for treatment-related AEs in older bevacizumab recipients. Patients and Methods: Patients age >= 65 were identified from SEER-Medicare and categorized by mCRC diagnosis pre and post bevacizumab approval (2001-2003 vs. 2005-2007). Preexisting conditions known to increase bevacizumab-related AE risk were identified in the year before diagnosis. Factors associated with bevacizumab receipt were identified using logistic regression. Incidence rates for all AEs and specific serious AEs were determined. Risk factors for first AE were determined by competing risks regression. Results: Of 6821 patients, 3282 (48%) were diagnosed in 2005-2007 of whom 19% received first-line bevacizumab. Likelihood of bevacizumab receipt was lower in patients age >= 75 (odds ratio [OR], 0.41; 95% confidence interval [CI], 0.36-0.47), nonwhite patients (OR, 0.67; 95% CI, 0.55-0.81), patients with higher comorbidity index (OR, 0.52; 95% CI, 0.43-0.62), and patients with preexisting cerebrovascular disease (OR, 0.49; 95% CI, 0.33-0.73). AE incidence rate was not increased among first-line bevacizumab recipients relative to first-line chemotherapy recipients. In a competing risk regression adjusting for potential confounders, bevacizumab receipt (2005-2007) was not associated with an increased risk of first AE compared with chemotherapy alone (2001-2007) (hazard ratio, 0.97; 95% CI, 0.87-1.08). Conclusion: In an older mCRC population, bevacizumab receipt was less likely in older (age >= 75) nonwhite patients with preexisting cerebrovascular comorbidities. First-line bevacizumab was not associated with increased AE incidence or risk of first AE compared with chemotherapy alone. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:204 / +
页数:11
相关论文
共 22 条
  • [1] Ambs A, 2008, HEALTH CARE FINANC R, V29, P5
  • [2] [Anonymous], AV PACK INS
  • [3] [Anonymous], surveillance epidemiology and end results
  • [4] Comparison of toxicity profiles of fluorouracil versus oxaliplatin regimens in a large population-based cohort of elderly patients with colorectal cancer
    Cen, P.
    Liu, C.
    Du, X. L.
    [J]. ANNALS OF ONCOLOGY, 2012, 23 (06) : 1503 - 1511
  • [5] Chemotherapy and Survival Benefit in Elderly Patients With Advanced Non-Small-Cell Lung Cancer
    Davidoff, Amy J.
    Tang, Mei
    Seal, Brian
    Edelman, Martin J.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (13) : 2191 - 2197
  • [6] Bevacizumab Beyond First Progression Is Associated With Prolonged Overall Survival in Metastatic Colorectal Cancer: Results From a Large Observational Cohort Study (BRiTE)
    Grothey, Axel
    Sugrue, Mary M.
    Purdie, David M.
    Dong, Wei
    Sargent, Daniel
    Hedrick, Eric
    Kozloff, Mark
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (33) : 5326 - 5334
  • [7] Safety and efficacy of oxaliplatin and fluoropyrimidine regimens with or without bevacizumab as first-line treatment of metastatic colorectal cancer: Results of the TREE study
    Hochster, Howard S.
    Hart, Lowell L.
    Ramanathan, Ramesh K.
    Childs, Barrett H.
    Hainsworth, John D.
    Cohn, Allen L.
    Wong, Lucas
    Fehrenbacher, Louis
    Abubakr, Yousif
    Saif, M. Wasif
    Schwartzberg, Lee
    Hedrick, Eric
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (21) : 3523 - 3529
  • [8] Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer
    Hurwitz, H
    Fehrenbacher, L
    Novotny, W
    Cartwright, T
    Hainsworth, J
    Heim, W
    Berlin, J
    Baron, A
    Griffing, S
    Holmgren, E
    Ferrara, N
    Fyfe, G
    Rogers, B
    Ross, R
    Kabbinavar, F
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (23) : 2335 - 2342
  • [9] Registries and Randomized Trials in Assessing the Effects of Bevacizumab in Colorectal Cancer: Is There a Common Theme?
    Hurwitz, Herbert I.
    Lyman, Gary H.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (06) : 580 - 581
  • [10] A refined comorbidity measurement algorithm for claims-based studies of breast, prostate, colorectal, and lung cancer patients
    Klabunde, Carrie N.
    Legler, Julie M.
    Warren, Joan L.
    Baldwin, Laura-Mae
    Schrag, Deborah
    [J]. ANNALS OF EPIDEMIOLOGY, 2007, 17 (08) : 584 - 590