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酪氨酸激酶抑制剂治疗慢性髓性白血病患者的二次恶性肿瘤的发生率和结局。

Incidence and outcome of second malignancies in patients with chronic myeloid leukemia during treatment with tyrosine kinase inhibitors.

机构信息

Department of Hematology, Yokohama Municipal Citizen's Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, 240-8555, Japan.

Division of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

出版信息

Med Oncol. 2018 May 30;35(7):99. doi: 10.1007/s12032-018-1159-7.

DOI:10.1007/s12032-018-1159-7
PMID:29846829
Abstract

We performed a retrospective study to evaluate the incidence of second malignancies (SMs) in chronic myeloid leukemia (CML) patients treated with tyrosine kinase inhibitors (TKIs). We analyzed data from 339 patients with CML who were extracted from the CML Cooperative Study Group database. The standardized incidence ratio (SIR) was calculated to assess the risk of SMs using data from the Cancer Registries in Japan. The median follow-up was 65 months. SMs developed in 14 patients (4.1%, 10 men, 4 women) after the start of TKIs. The median age was 69 years at the time of the CML diagnosis and 72.5 years at the time of the SM diagnosis. Ten patients were treated with imatinib, three with dasatinib, and one with nilotinib as the initial treatment. The SIR for all malignancies was 1.05 (95% CI 0.50-1.93) for men and 1.08 (95% CI 0.29-2.76) for women. The difference in the overall survival (OS) of patients with or without SMs was not statistically significant (5-year OS: 82.5% vs. 92.9%; p = 0.343). A subgroup analysis of 166 patients treated with second-generation TKIs (92 dasatinib, 74 nilotinib) showed that the SIRs for all malignancies were 1.33 (95% CI 0.36-3.41) for men and 0 for women. In conclusion, the incidence of SMs in CML patients during TKI treatment was the same as that in the general Japanese population. There was no evidence of an increase in the incidence of SMs during second-generation TKI treatment. Furthermore, the occurrence of SMs during TKI treatment did not affect the survival or mortality in our cohort.

摘要

我们进行了一项回顾性研究,以评估接受酪氨酸激酶抑制剂 (TKI) 治疗的慢性髓性白血病 (CML) 患者的第二恶性肿瘤 (SM) 发生率。我们分析了从 CML 合作研究组数据库中提取的 339 名 CML 患者的数据。使用日本癌症登记处的数据计算标准化发病比 (SIR),以评估 SM 的风险。中位随访时间为 65 个月。在开始 TKI 治疗后,14 名患者(4.1%,10 名男性,4 名女性)发生 SM。CML 诊断时的中位年龄为 69 岁,SM 诊断时的中位年龄为 72.5 岁。10 名患者初始治疗使用伊马替尼,3 名患者使用达沙替尼,1 名患者使用尼洛替尼。男性所有恶性肿瘤的 SIR 为 1.05(95%CI 0.50-1.93),女性为 1.08(95%CI 0.29-2.76)。有或没有 SM 的患者的总生存(OS)差异无统计学意义(5 年 OS:82.5% vs. 92.9%;p=0.343)。对 166 名接受第二代 TKI 治疗的患者(92 名达沙替尼,74 名尼洛替尼)进行的亚组分析显示,男性所有恶性肿瘤的 SIR 为 1.33(95%CI 0.36-3.41),女性为 0。总之,TKI 治疗期间 CML 患者的 SM 发生率与日本普通人群相同。第二代 TKI 治疗期间没有证据表明 SM 发生率增加。此外,TKI 治疗期间发生 SM 并未影响我们队列的生存或死亡率。

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