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CDK 4/6抑制剂与姑息性放疗联合使用时毒性增强:非连续性病例系列及文献综述

Enhanced toxicity with CDK 4/6 inhibitors and palliative radiotherapy: Non-consecutive case series and review of the literature.

作者信息

David Steven, Ho Gwo, Day Daphne, Harris Marion, Tan Jennifer, Goel Shom, Hanna Gerard G, Srivastava Ranjana, Kruss Gill, McDowell Lachlan, White Michelle

机构信息

Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia; Monash Cancer Centre, East Bentleigh, VIC, Australia.

Monash Cancer Centre, East Bentleigh, VIC, Australia; School of Clinical Sciences, Monash University, Clayton, VIC, Australia.

出版信息

Transl Oncol. 2021 Jan;14(1):100939. doi: 10.1016/j.tranon.2020.100939. Epub 2020 Nov 20.

Abstract

Current first-line systemic treatment in most patients with metastatic hormone receptor-positive, HER-2 negative breast cancer is an aromatase inhibitor in combination with a cyclin dependant kinase (CDK) 4/6 inhibitor. Frequently, these patients require palliative radiotherapy (RT) for symptomatic disease management. There is a paucity of data on the safety of combining a CDK 4/6 inhibitor with palliative RT, with conflicting case reports in the literature. We report on 5 cases at our institution where enhanced radiotherapy toxicity was observed when palliative doses of RT was delivered during or prior to treatment with a CDK 4/6 inhibitor. After review of pre-clinical and mechanistic data, we hypothesise that the effects of CDK4/6 inhibition on normal tissue and the tumour microenvironment may impede tissue recovery and exacerbate acute radiation and radiation recall toxicities. Further studies are required to clarify the potential toxicities of this combination. Clinicians should consider the potential risks when combining CDK 4/6 inhibitors with palliative RT and individualise patient management accordingly.

摘要

目前,大多数转移性激素受体阳性、HER-2阴性乳腺癌患者的一线全身治疗方案是芳香化酶抑制剂联合细胞周期蛋白依赖性激酶(CDK)4/6抑制剂。这些患者通常需要姑息性放疗(RT)来控制症状性疾病。关于CDK 4/6抑制剂与姑息性放疗联合应用的安全性数据较少,文献中的病例报告相互矛盾。我们报告了我院的5例病例,这些病例在接受CDK 4/6抑制剂治疗期间或之前给予姑息性放疗剂量时,观察到放疗毒性增强。在回顾临床前和机制数据后,我们推测CDK4/6抑制对正常组织和肿瘤微环境的影响可能会阻碍组织恢复,并加重急性放射和放射回忆毒性。需要进一步研究来阐明这种联合治疗的潜在毒性。临床医生在将CDK 4/6抑制剂与姑息性放疗联合应用时应考虑潜在风险,并据此对患者进行个体化管理。

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