Literature DB >> 23864097

Primary tumor location and bevacizumab effectiveness in patients with metastatic colorectal cancer.

M K Boisen1, J S Johansen, C Dehlendorff, J S Larsen, K Osterlind, J Hansen, S E Nielsen, P Pfeiffer, L S Tarpgaard, N H Holländer, N Keldsen, T F Hansen, B B Jensen, B V Jensen.   

Abstract

BACKGROUND: There is an unmet need for predictive markers for the antiangiogenic agent bevacizumab in metastatic colorectal cancer (mCRC). We aimed to assess whether the location of the primary tumor is associated with bevacizumab effectiveness when combined with capecitabine and oxaliplatin (CAPEOX) in the first-line treatment of patients with mCRC. PATIENTS AND METHODS: A cohort of 667 consecutive patients with mCRC from the general community treated from 2006 to 2011 with CAPEOX and bevacizumab as standard first-line therapy was compared with a cohort of 213 patients treated with CAPEOX from 2003 to 2006, before bevacizumab was approved. Main outcome measures were progression-free survival (PFS) and overall survival (OS). Differences in outcome were tested using Kaplan-Meier curves and log-rank tests, and multivariate analyses were carried out using Cox Proportional Hazards models.
RESULTS: Patients treated with CAPEOX and bevacizumab with primary tumors originating in the sigmoid colon and rectum had a significantly better outcome than patients with primary tumors originating from the cecum to the descending colon, both for PFS (median PFS 9.3 versus 7.2 months; hazard ratio (HR) 0.68, 95% confidence interval (CI) 0.56-0.82) and for OS (median OS 23.5 versus 13.0 months; HR 0.47, 95% CI 0.38-0.57). This difference was confirmed in multivariate analyses after adjustment for other potentially prognostic factors. For patients treated with CAPEOX, there was no association between primary tumor location and outcome, neither in unadjusted nor adjusted analyses.
CONCLUSIONS: The addition of bevacizumab to CAPEOX in first-line treatment of patients with mCRC may primarily benefit patients with primary tumors originating in the rectum and sigmoid colon. This hypothesis needs to be validated in data from completed randomized trials. CLINICALTRIALSGOV IDENTIFICATION NUMBER: NCT00212615.

Entities:  

Keywords:  bevacizumab; biomarker; chemotherapy; metastatic colorectal cancer; primary tumor

Mesh:

Substances:

Year:  2013        PMID: 23864097     DOI: 10.1093/annonc/mdt253

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


  34 in total

Review 1.  Colorectal Cancer: Why Does Side Matter?

Authors:  Claire Gallois; Simon Pernot; Aziz Zaanan; Julien Taieb
Journal:  Drugs       Date:  2018-06       Impact factor: 9.546

2.  Genes involved in pericyte-driven tumor maturation predict treatment benefit of first-line FOLFIRI plus bevacizumab in patients with metastatic colorectal cancer.

Authors:  N B Volz; S Stintzing; W Zhang; D Yang; Y Ning; T Wakatsuki; R E El-Khoueiry; J E Li; A Kardosh; F Loupakis; C Cremolini; A Falcone; S J Scherer; H-J Lenz
Journal:  Pharmacogenomics J       Date:  2014-07-29       Impact factor: 3.550

3.  Racial Differences in Stage IV Colorectal Cancer Survival in Younger and Older Patients.

Authors:  Kristin Wallace; Allan DeToma; David N Lewin; Shaoli Sun; Don Rockey; Carolyn D Britten; Jennifer D Wu; Aissatou Ba; Anthony J Alberg; Elizabeth G Hill
Journal:  Clin Colorectal Cancer       Date:  2016-12-07       Impact factor: 4.481

4.  Embryonic Origin of Primary Colon Cancer Predicts Pathologic Response and Survival in Patients Undergoing Resection for Colon Cancer Liver Metastases.

Authors:  Suguru Yamashita; Kristoffer Watten Brudvik; Scott E Kopetz; Dipen Maru; Callisia N Clarke; Guillaume Passot; Claudius Conrad; Yun Shin Chun; Thomas A Aloia; Jean-Nicolas Vauthey
Journal:  Ann Surg       Date:  2018-03       Impact factor: 12.969

Review 5.  Different treatment strategies and molecular features between right-sided and left-sided colon cancers.

Authors:  Hong Shen; Jiao Yang; Qing Huang; Meng-Jie Jiang; Yi-Nuo Tan; Jian-Fei Fu; Li-Zhen Zhu; Xue-Feng Fang; Ying Yuan
Journal:  World J Gastroenterol       Date:  2015-06-07       Impact factor: 5.742

6.  Primary tumor location as a prognostic factor in metastatic colorectal cancer.

Authors:  Fotios Loupakis; Dongyun Yang; Linda Yau; Shibao Feng; Chiara Cremolini; Wu Zhang; Martin K H Maus; Carlotta Antoniotti; Christiane Langer; Stefan J Scherer; Thomas Müller; Herbert I Hurwitz; Leonard Saltz; Alfredo Falcone; Heinz-Josef Lenz
Journal:  J Natl Cancer Inst       Date:  2015-02-24       Impact factor: 13.506

7.  Patients with distal intestinal gastric cancer have superior outcome with addition of taxanes to combination chemotherapy, while proximal intestinal and diffuse gastric cancers do not: does biology and location predict chemotherapy benefit?

Authors:  Ali Murat Sedef; Fatih Köse; Ahmet Taner Sümbül; Özlem Doğan; Ali Ayberk Beşen; Ali Murat Tatlı; Hüseyin Mertsoylu; Ahmet Sezer; Sadık Muallaoğlu; Özgür Özyılkan; Hüseyin Abalı
Journal:  Med Oncol       Date:  2015-01-09       Impact factor: 3.064

Review 8.  Prognostic factors for survival with bevacizumab-based therapy in colorectal cancer patients: a systematic review and pooled analysis of 11,585 patients.

Authors:  Fausto Petrelli; Andrea Coinu; Mary Cabiddu; Karen Borgonovo; Veronica Lonati; Mara Ghilardi; Sandro Barni
Journal:  Med Oncol       Date:  2015-01-09       Impact factor: 3.064

9.  Association of Primary Tumor Site With Mortality in Patients Receiving Bevacizumab and Cetuximab for Metastatic Colorectal Cancer.

Authors:  Mayada A Aljehani; John W Morgan; Laurel A Guthrie; Brice Jabo; Majed Ramadan; Khaled Bahjri; Sharon S Lum; Matthew Selleck; Mark E Reeves; Carlos Garberoglio; Maheswari Senthil
Journal:  JAMA Surg       Date:  2018-01-01       Impact factor: 14.766

10.  Prognostic and predictive value of primary tumour side in patients with RAS wild-type metastatic colorectal cancer treated with chemotherapy and EGFR directed antibodies in six randomized trials.

Authors:  D Arnold; B Lueza; J-Y Douillard; M Peeters; H-J Lenz; A Venook; V Heinemann; E Van Cutsem; J-P Pignon; J Tabernero; A Cervantes; F Ciardiello
Journal:  Ann Oncol       Date:  2017-08-01       Impact factor: 32.976

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