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Bevacizumab plus irinotecan-based therapy in metastatic colorectal cancer patients previously treated with oxaliplatin-based regimens.

Authors :
Yildiz R
Buyukberber S
Uner A
Yamac D
Coskun U
Kaya AO
Ozturk B
Yaman E
Benekli M
Yildiz, Ramazan
Buyukberber, Suleyman
Uner, Aytug
Yamac, Deniz
Coskun, Ugur
Kaya, Ali Osman
Ozturk, Banu
Yaman, Emel
Benekli, Mustafa
Source :
Cancer Investigation; Feb2010, Vol. 28 Issue 1, p33-37, 5p
Publication Year :
2010

Abstract

<bold>Background: </bold>Treatment of patients with metastatic colorectal cancer (MCRC) previously exposed to oxaliplatin-based regimen is challenging. Efficacy and toxicity of bevacizumab plus irinotecan-based regimens were assessed in the second-line treatment of MCRC patients.<bold>Patients and Methods: </bold>Forty patients with a median age of 53 years (range, 31-75) were retrospectively evaluated. Patients progressing or relapsing after treatment with oxaliplatin-based regimens were given bevacizumab 5 mg/kg every 2 weeks in combination with irinotecan-based regimens. All patients had previously received oxaliplatin either in the adjuvant setting (n = 8) or for metastatic disease (n = 32).<bold>Results: </bold>Three patients achieved a complete response (7.5%), 5 partial responses (12.5%) and 14 (35%) stable disease resulting in an overall response rate of 20%. Median progression-free survival was 6 months (95% CI, 4.0-8.0) with a median overall survival of 14 months (95% CI, 10.2-17.8). One-year survival rate was 55.9%. Grade 3-4 toxicities were as follows: neutropenia (n = 15, 37.5%), febrile neutropenia (n = 2, 5%), diarrhea (n = 11, 27.5%), nausea and vomiting (n = 3, 7.5%), gastrointestinal perforation (n = 2, 5%), and thromboembolism (n = 2, 5%).<bold>Conclusion: </bold>Bevacizumab plus irinotecan-based combination chemotherapy is an active and safe treatment option in patients failing oxaliplatin-based therapy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07357907
Volume :
28
Issue :
1
Database :
Complementary Index
Journal :
Cancer Investigation
Publication Type :
Academic Journal
Accession number :
105284952
Full Text :
https://doi.org/10.3109/07357900802562996