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利用美国食品和药物管理局不良事件报告系统(FAERS)分析实体器官肿瘤化疗后继发性白血病和骨髓增生异常综合征。

Analysis of Secondary Leukemia and Myelodysplastic Syndrome After Chemotherapy for Solid Organ Tumors Using the Food and Drug Administration Adverse Event Reporting System (FAERS).

机构信息

Department of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University.

Education and Research Center for Clinical Pharmacy, Osaka University of Pharmaceutical Sciences, Osaka, Japan.

出版信息

J Pharm Pharm Sci. 2021;24:499-508. doi: 10.18433/jpps31862.

Abstract

PURPOSE

As the prognosis of cancer patients deteriorates, secondary carcinogenesis after chemotherapy, especially secondary hematological malignancies, becomes a serious problem. However, information on the frequency and time of onset of secondary hematological malignancies and the risk of hematological malignancy with different drugs is scarce. This study aimed to evaluate the incidence of leukemia and myelodysplastic syndrome in patients with solid tumors, including breast, colon, gastric, pancreatic, small cell lung, non-small cell lung, esophageal, ovarian, cervical, and endometrial cancers.

METHODS

Using the United States Food and Drug Administration Adverse Event Reporting System, we analyzed the reporting rates, reporting odds ratios, and the reporting onset times of secondary leukemia and myelodysplastic syndrome for each drug used.

RESULTS

The leukemia reporting rates were higher in breast, small cell lung, ovarian, and endometrial cancers than in other cancers, and the myelodysplastic syndrome reporting rates were higher in ovarian and endometrial cancers than in other cancers. For each cancer type, the reporting odds ratios of cytocidal anticancer agents, such as taxanes, anthracyclines, alkylating agents, platinum, and topoisomerase inhibitors, were higher than those of other drugs. Alternatively, the reporting odds ratios of molecular targeted drugs and immune checkpoint inhibitors were not higher than those of other drugs. Approximately half of the cases of leukemia and myelodysplastic syndrome were reported within 1 to 4 years after chemotherapy.

CONCLUSIONS

Our study clarified the risks of leukemia and myelodysplastic syndrome for several anticancer drugs in patients with solid tumors. Our data may aid in the assessment of the risks of secondary leukemia and myelodysplastic syndrome when medical oncologists, clinical pharmacists, and patients select chemotherapy regimens.

摘要

目的

随着癌症患者预后的恶化,化疗后继发癌发生,尤其是继发血液系统恶性肿瘤,成为一个严重的问题。然而,关于继发血液系统恶性肿瘤的发生频率和时间以及不同药物发生血液系统恶性肿瘤的风险的信息却很少。本研究旨在评估包括乳腺癌、结肠癌、胃癌、胰腺癌、小细胞肺癌、非小细胞肺癌、食管癌、卵巢癌、宫颈癌和子宫内膜癌在内的实体瘤患者发生白血病和骨髓增生异常综合征的情况。

方法

我们使用美国食品和药物管理局不良事件报告系统,分析了每种药物继发白血病和骨髓增生异常综合征的报告率、报告比值比和报告发病时间。

结果

乳腺癌、小细胞肺癌、卵巢癌和子宫内膜癌的白血病报告率高于其他癌症,而卵巢癌和子宫内膜癌的骨髓增生异常综合征报告率高于其他癌症。对于每种癌症类型,细胞毒性抗癌药物(如紫杉烷类、蒽环类药物、烷化剂、铂类和拓扑异构酶抑制剂)的报告比值比高于其他药物。相反,分子靶向药物和免疫检查点抑制剂的报告比值比并不高于其他药物。大约一半的白血病和骨髓增生异常综合征病例是在化疗后 1 至 4 年内报告的。

结论

本研究阐明了几种用于实体瘤患者的抗癌药物发生白血病和骨髓增生异常综合征的风险。当肿瘤内科医生、临床药师和患者选择化疗方案时,我们的数据可能有助于评估继发白血病和骨髓增生异常综合征的风险。

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