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免疫检查点抑制剂纳武单抗与放疗联合用于经治肺癌患者:联合治疗的疗效与安全性

Immune Checkpoint Inhibitor Nivolumab and Radiotherapy in Pretreated Lung Cancer Patients: Efficacy and Safety of Combination.

作者信息

Fiorica Francesco, Belluomini Lorenzo, Stefanelli Antonio, Santini Alessandra, Urbini Benedetta, Giorgi Carlotta, Frassoldati Antonio

机构信息

Departments of *Radiation Oncology †Medical Oncology, University Hospital ‡Department of Oncology and Experimental Biology, Laboratory for Technologies of Advanced Therapies (LTTA), University of Ferrara, Ferrara, Italy.

出版信息

Am J Clin Oncol. 2018 Nov;41(11):1101-1105. doi: 10.1097/COC.0000000000000428.

Abstract

BACKGROUND

In the last decade, the discovery of immune checkpoint inhibitors such as the PD-1 inhibitor, nivolumab, has revolutionized the treatment of advanced non-small cell lung cancer (NSCLC). Concurrent radiotherapy (RT) is of particular interest in showing the potential role of the combination.

OBJECTIVE

The purpose of this study was to retrospectively evaluate the addition of RT to an immune checkpoint inhibitor, nivolumab, with regard to activity and feasibility in pretreated, advanced, or metastatic lung cancer patients at our center.

PATIENTS AND METHODS

We retrospectively identified 35 consecutive patients (30 men and 5 women), who received nivolumab for pretreated NSCLC, between March 2015 to December 2016. Fifteen received hypofractionated RT as a palliative measure, and, in these patients, nivolumab was administered at an interval of at least 1 week from the end of RT.

RESULTS

The median age was 69 years, and 23 patients (65.7%) had an Eastern Cooperative Oncology Group (ECOG) score of 0 to 1. All patients had previously received at least 1 systemic regimen, and, for only 3 (8.6%), nivolumab was a third-line treatment. The 2 treatment arms, RT-nivolumab and only-nivolumab, were well matched for baseline characteristics. At a median follow-up of 7.4 months, the 1-year overall survival rates were 57.8% for patients treated with RT-nivolumab and 27.4% for patients treated with only-nivolumab (P=0.043). The 1-year progression-free survival in the RT-nivolumab group was 57.8% and 20.6% in the only-nivolumab group (P=0.040). No difference in adverse events was detected.

CONCLUSIONS

In conclusion, RT and nivolumab can be combined, obtaining a benefit in overall survival and progression-free survival, without an increase in acute toxicities in pretreated advanced NSCLC patients. Prospective studies are needed to confirm these results.

摘要

背景

在过去十年中,诸如程序性死亡受体1(PD-1)抑制剂纳武单抗等免疫检查点抑制剂的发现,彻底改变了晚期非小细胞肺癌(NSCLC)的治疗方式。同步放疗(RT)在显示联合治疗的潜在作用方面尤其令人关注。

目的

本研究的目的是回顾性评估在我们中心,对经治的晚期或转移性肺癌患者,在免疫检查点抑制剂纳武单抗治疗基础上加用放疗的活性和可行性。

患者与方法

我们回顾性纳入了2015年3月至2016年12月期间连续接受纳武单抗治疗的35例经治NSCLC患者(30例男性和5例女性)。15例接受了短程分割放疗作为姑息治疗措施,在这些患者中,纳武单抗在放疗结束后至少间隔1周给药。

结果

中位年龄为69岁,23例患者(65.7%)东部肿瘤协作组(ECOG)评分为0至1分。所有患者此前均至少接受过1种全身治疗方案,仅3例(8.6%)患者将纳武单抗作为三线治疗。放疗联合纳武单抗组和单纯纳武单抗组在基线特征方面匹配良好。中位随访7.4个月时,放疗联合纳武单抗组患者的1年总生存率为57.8%,单纯纳武单抗组为27.4%(P = 0.043)。放疗联合纳武单抗组的1年无进展生存率为57.8%(单纯纳武单抗组为20.6%,P = 0.040)。未检测到不良事件有差异。

结论

总之,放疗和纳武单抗可以联合使用,在经治的晚期NSCLC患者中可提高总生存率和无进展生存率,且不增加急性毒性。需要进行前瞻性研究来证实这些结果。

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