医学
慢性粒细胞白血病
伊马替尼
甲磺酸伊马替尼
内科学
中性粒细胞减少症
胃肠病学
白细胞减少症
白血病
肿瘤科
化疗
髓系白血病
作者
Thomas B. Sneed,Hagop M. Kantarjian,Moshe Talpaz,Susan O’Brien,Mary Beth Rios,B. Nebiyou Bekele,Xian Zhou,Debra Resta,William Wierda,Stefan Faderl,Francis J. Giles,Jorge E. Cortés
出处
期刊:Cancer
[Wiley]
日期:2003-11-18
卷期号:100 (1): 116-121
被引量:123
摘要
Abstract BACKGROUND Imatinib mesylate induces high rates of hematologic and cytogenetic response in patients with chronic myelogenous leukemia (CML). During therapy with imatinib, up to 45% of patients with CML reportedly experience myelosuppression ≥ Grade 3, requiring interruption of therapy and/or dose reductions. The significance of myelosuppression for response to imatinib is unknown. METHODS The authors analyzed 143 patients with late chronic‐phase CML who were treated with imatinib after failing interferon. Univariate and multivariate analyses were performed to determine patient characteristics that were correlated with myelosuppression response and the association between myelosuppression and cytogenetic response. RESULTS Neutropenia ≥ Grade 3 (according to National Cancer Institute Common Toxicity Criteria) occurred in 64 patients (45%), and thrombocytopenia ≥ Grade 3 occurred in 31 patients (22%). Any myelosuppression ≥ Grade 3 was associated with a lower rate of major ( P = 0.04) or complete ( P = 0.01) cytogenetic responses. This was more pronounced with myelosuppression that lasted > 2 weeks. The major cytogenetic response rate was 58% with Grade ≥ 3 myelosuppression compared with a rate of 75% without Grade ≥3 myelosuppression ( P = 0.03); the complete cytogenetic response rates were 36% and 63%, respectively ( P = 0.001). In a multivariate analysis, pretreatment platelet count, imatinib dose reductions, and duration of myelosuppression were associated significantly with response. CONCLUSIONS Myelosuppression is an independent adverse factor for achieving cytogenetic response with imatinib in patients with CML. Intervention with hematopoietic growth factors in patients with CML who are treated with imatinib should be investigated. Cancer 2004;100:116–21. © 2003 American Cancer Society.
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