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病例报告:在奥希替尼耐药期间确诊急性早幼粒细胞白血病,随后使用粒细胞集落刺激因子和帕博利珠单抗治疗。

Case report: Identification of acute promyelocytic leukemia during osimertinib resistance followed by granulocyte colony-stimulating factor and pembrolizumab.

作者信息

Tian Huohuan, Yang Linhui, Hou Wang, Wu Yu, Dai Yang, Yu Jiang, Liu Dan

机构信息

Department of Respiratory and Critical Care Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan,  China.

Department of Hematology, West China Hospital, Sichuan University, Chengdu, Sichuan,  China.

出版信息

Front Oncol. 2023 Jan 13;12:1032225. doi: 10.3389/fonc.2022.1032225. eCollection 2022.

Abstract

BACKGROUND

The occurrence of acute promyelocytic leukemia (APL) during the management of lung cancer is rare and life-threatening. It was mainly reported to be secondary to chemoradiotherapy. A few studies reported an increased incidence of therapy-related acute promyelocytic leukemia (t-APL) after gefitinib became available.

CASE PRESENTATION

We reported a patient who developed thrombocytopenia after receiving oral osimertinib in combination with intensity-modulated radiotherapy (IMRT). For half a year, she had an unrecoverable low platelet count, which progressed to concomitant leukopenia and the transient appearance of orthochromatic normoblasts in the peripheral blood test, indicating a dormant myeloid disorder. Due to simultaneous resistance to epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKI), pembrolizumab and granulocyte colony-stimulating factor (G-CSF) were administered, revealing prominent signs of hematological malignancy in a peripheral blood test that was later identified as t-APL.

CONCLUSION

In general, patients undergoing EGFR-TKI combined with local radiotherapy should be concerned about their hematological assessment. If patients exhibit unrecoverable abnormalities in routine blood tests, a secondary nonsolid malignancy other than myelosuppression should be considered, and further lung cancer treatment should be discontinued.

摘要

背景

肺癌治疗期间发生急性早幼粒细胞白血病(APL)较为罕见且危及生命。主要报道其继发于放化疗。有少数研究报道吉非替尼上市后治疗相关急性早幼粒细胞白血病(t-APL)的发病率有所增加。

病例介绍

我们报告了一名患者,在接受口服奥希替尼联合调强放疗(IMRT)后出现血小板减少。半年来,她的血小板计数持续处于无法恢复的低水平,进而发展为同时伴有白细胞减少,外周血检查出现正染早幼粒细胞短暂出现,提示存在潜在的骨髓疾病。由于对表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKI)同时耐药,给予了帕博利珠单抗和粒细胞集落刺激因子(G-CSF),外周血检查显示出明显的血液系统恶性肿瘤迹象,后来确诊为t-APL。

结论

一般来说,接受EGFR-TKI联合局部放疗的患者应关注其血液学评估。如果患者在常规血液检查中出现无法恢复的异常,应考虑除骨髓抑制之外的继发性非实体恶性肿瘤,并应停止进一步的肺癌治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d99/9880289/718014515852/fonc-12-1032225-g001.jpg

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