We retrospectively analysed 153 patients with metastatic colorectal cancer who received FOLFOX with or without bevacizumab as first-line chemotherapy. Several background characteristics and chemotherapy features (grade of neutropaenia, use of bevacizumab or irinotecan, re-introduction of FOLFOX, and tumour progression) as time-varying covariates were analysed as potential prognostic factors. Of the 153 patients, mild neutropaenia (grade 1-2) occurred in 60 patients (39%) and severe neutropaenia (grade 3-4) occurred in 46 patients (30%). The other 47 patients (31%) did not experience neutropaenia. According to a multivariate Cox model with time-varying covariates, hazard ratios (HRs) of death were 0.55 (95% confidence interval (CI), 0.31-0.98; P = 0.044) for patients with mild neutropaenia and 0.35 (95% Cl, 0.18-0.66; P = 0.002) for those with severe neutropaenia. Both mild and severe neutropaenia during chemotherapy are associated with improved survival in patients with MCRC. Prospective trials are required to assess whether dosing adjustments based on neutropaenia may improve chemotherapy efficacy. Crown Copyright (C) 2009 Published by Elsevier Ltd. All rights reserved.
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St Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Natl Canc Ctr, Div Canc Immunotherapy, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Tada, K.
Shoji, H.
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Natl Canc Ctr, Gastrointestinal Med Oncol Div, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Shoji, H.
Kitano, S.
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Natl Canc Ctr, Dept Expt Therapeut, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Kitano, S.
Nishimura, T.
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Tokyo Jikei Med Univ, Gastrointestinal Med Div, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Nishimura, T.
Shimada, Y.
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Natl Canc Ctr, Gastrointestinal Med Oncol Div, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Shimada, Y.
Nagashima, K.
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Chiba Univ, Dept Global Clin Res, Chiba, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Nagashima, K.
Ito, A.
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Natl Canc Ctr, Hematopoietci Stem Cell Transplant Div, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Ito, A.
Honma, Y.
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Natl Canc Ctr, Gastrointestinal Med Oncol Div, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Honma, Y.
Iwasa, S.
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Natl Canc Ctr, Gastrointestinal Med Oncol Div, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Iwasa, S.
Okita, N.
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Natl Canc Ctr, Gastrointestinal Med Oncol Div, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Okita, N.
Takashima, A.
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Natl Canc Ctr, Gastrointestinal Med Oncol Div, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Takashima, A.
Kato, K.
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Natl Canc Ctr, Gastrointestinal Med Oncol Div, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Kato, K.
Yamada, Y.
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Natl Canc Ctr, Gastrointestinal Med Oncol Div, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Yamada, Y.
Katayama, N.
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Mie Univ, Dept Hematol & Oncol, Tsu, Mie 514, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Katayama, N.
Boku, N.
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Natl Canc Ctr, Gastrointestinal Med Oncol Div, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Boku, N.
Heike, Y.
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St Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan
Heike, Y.
Hamaguchi, T.
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Natl Canc Ctr, Gastrointestinal Med Oncol Div, Tokyo, JapanSt Lukes Int Hosp, Immunotherapy & Cell Therapy Serv, Tokyo, Japan