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酪氨酸激酶抑制剂治疗慢性髓性白血病期间第二原发性恶性肿瘤的发生率

Incidence of Second Malignancies of Chronic Myeloid Leukemia During Treatment With Tyrosine Kinase Inhibitors.

作者信息

Yin Xiu-Feng, Wang Jing-Han, Li Xia, Yu Meng-Xia, Ma Zhi-Xin, Jin Jie

机构信息

Institute of Hematology, Zhejiang University School of Medicine, Hangzhou, P.R. China.

Department of Hematology, the First Affiliated Hospital of Zhejiang University, School of Medicine, Hangzhou, P.R. China.

出版信息

Clin Lymphoma Myeloma Leuk. 2016 Oct;16(10):577-581. doi: 10.1016/j.clml.2016.06.010. Epub 2016 Jun 8.

Abstract

BACKGROUND

Tyrosine kinase inhibitors (TKIs) have revolutionized the treatment of chronic myeloid leukemia (CML) by providing patients with long-term survival. Although most patients who receive TKI treatment have shown satisfactory tolerance, second malignancies (SMs) should not be ignored because of lifetime treatment. We designed a retrospective study to evaluate the incidence and possible risk factors of SMs in CML patients treated with TKIs.

PATIENTS AND METHODS

Records of 223 patients with Philadelphia chromosome-positive CML treated with imatinib were reviewed to investigate frequencies and characteristics of SMs. The data of SMs were compared with the number expected from the National Central Cancer Registry. The possible risk factors of SM in CML patients treated with TKIs were also evaluated using Poisson regression in this study.

RESULTS

After a median follow-up of 64 months (range, 4-253 months) from CML diagnosis, 7 patients (3.14%) developed 6 different SMs including colon, stomach, breast, kidney, cervical, and lymphonodus tissue. The risk of second cancer was higher than expected (observed-to-expected ratio, 2.45; 95% confidence interval, 1.17-5.14; P = .018). No associated elements were found in terms of influencing the incidence of SM in CML patients treated with TKIs.

CONCLUSION

We found patients with CML treated with TKIs had a higher relative incidence of SM compared with the expected incidence among the general Chinese population. However, the correlations between second cancer and the potential risk factors including the length of exposure and cumulative dose of TKIs were not found in this study.

摘要

背景

酪氨酸激酶抑制剂(TKIs)通过为患者提供长期生存,彻底改变了慢性髓性白血病(CML)的治疗方式。尽管大多数接受TKI治疗的患者耐受性良好,但由于需要终身治疗,第二原发性恶性肿瘤(SMs)不容忽视。我们设计了一项回顾性研究,以评估接受TKIs治疗的CML患者中SMs的发生率及可能的危险因素。

患者与方法

回顾了223例接受伊马替尼治疗的费城染色体阳性CML患者的记录,以调查SMs的发生频率和特征。将SMs的数据与国家中央癌症登记处预期的数量进行比较。本研究还使用泊松回归评估了接受TKIs治疗的CML患者发生SM的可能危险因素。

结果

自CML诊断起,中位随访64个月(范围4 - 253个月)后,7例患者(3.14%)发生了6种不同的SM,包括结肠癌、胃癌、乳腺癌、肾癌、宫颈癌和淋巴结组织癌。第二原发性癌症的风险高于预期(观察值与预期值之比为2.45;95%置信区间为1.17 - 5.14;P = 0.018)。在接受TKIs治疗的CML患者中,未发现影响SM发生率的相关因素。

结论

我们发现,与中国普通人群的预期发生率相比,接受TKIs治疗的CML患者发生SM的相对发生率更高。然而,本研究未发现第二原发性癌症与包括TKI暴露时间和累积剂量在内的潜在危险因素之间的相关性。

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