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广泛期小细胞肺癌化疗免疫治疗后药物性间质性肺疾病

Drug-induced interstitial lung disease after chemoimmunotherapy for extensive-stage small cell lung cancer.

作者信息

Fukuda Kiyoko, Katsurada Naoko, Kawa Yoshitaka, Satouchi Miyako, Kaneshiro Kazumi, Matsumoto Masataka, Takamiya Rei, Hatakeyama Yukihisa, Dokuni Ryota, Matsumura Kanoko, Katsurada Masahiro, Nakata Kyosuke, Yoshimura Sho, Tachihara Motoko

机构信息

Division of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Japan.

Department of Thoracic Oncology, Hyogo Cancer Center, Japan.

出版信息

Heliyon. 2023 Sep 26;9(10):e20463. doi: 10.1016/j.heliyon.2023.e20463. eCollection 2023 Oct.

Abstract

OBJECTIVES

The combination of chemotherapy and immune checkpoint inhibitors (chemo-ICI) has become the new standard of treatment for extensive-stage small cell lung cancer (ES-SCLC). Recently, slight changes in interstitial shadows, defined as interstitial lung abnormalities (ILA), have been identified. In patients with ES-SCLC who received chemo-ICI, there are limited data on the incidence of drug-induced interstitial lung disease (D-ILD) in daily practice and the association between the development of D-ILD and ILA in the baseline computed tomography (CT).

MATERIALS AND METHODS

A multicenter, retrospective study was conducted to investigate the incidence of D-ILD, the risk factors for developing D-ILD, progression-free survival (PFS), and overall survival (OS) in patients with ES-SCLC who received chemo-ICI between August 2019 and November 2021.

RESULTS

This study enrolled 70 patients (median age, 71 years; including 58 men) from nine institutions in Japan. There were 62 patients (89%) treated with carboplatin/etoposide/atezolizumab and 8 patients treated with carboplatin or cisplatin/etoposide/durvalumab. Twenty-nine patients (41.4%) were found to have ILA at baseline CT. Eleven patients (15.7%) developed D-ILD. The proportion of patients with ILA was significantly higher in the group who developed D-ILD than in the group who did not (9/11 (81.8%) vs. 20/59 (33.9%), respectively, P = 0.0057). In addition, the frequency of ground glass attenuation (GGA) and reticulation was higher in patients who developed D-ILD. There was no significant difference in PFS and OS between patients who developed D-ILD and those who did not (median PFS, 8.0 (95% confidence interval (CI), 5.5-9.5) months vs. 5.0 (95% CI, 4.5-5.6) months, respectively, P = 0.11 and median OS, not reached (NR) (95% CI, 8.7-NR) vs. 18.2 (95% CI, 13.2-NR) months, respectively, P = 0.20).

CONCLUSION

The incidence of D-ILD in patients with ES-SCLC who received chemo-ICI in clinical practice was higher than that in clinical trials. Patients with pre-existing ILA were more likely to develop D-ILD.

摘要

目的

化疗与免疫检查点抑制剂联合治疗(化疗-免疫检查点抑制剂联合治疗)已成为广泛期小细胞肺癌(ES-SCLC)的新治疗标准。最近,已发现间质阴影出现轻微变化,定义为间质性肺异常(ILA)。在接受化疗-免疫检查点抑制剂联合治疗的ES-SCLC患者中,关于日常实践中药物性间质性肺病(D-ILD)的发生率以及基线计算机断层扫描(CT)中D-ILD的发生与ILA之间的关联的数据有限。

材料与方法

进行了一项多中心回顾性研究,以调查2019年8月至2021年11月期间接受化疗-免疫检查点抑制剂联合治疗的ES-SCLC患者中D-ILD的发生率、发生D-ILD的危险因素、无进展生存期(PFS)和总生存期(OS)。

结果

本研究纳入了来自日本9家机构的70例患者(中位年龄71岁;包括58名男性)。62例患者(89%)接受了卡铂/依托泊苷/阿特珠单抗治疗,8例患者接受了卡铂或顺铂/依托泊苷/度伐利尤单抗治疗。29例患者(41.4%)在基线CT检查时发现有ILA。11例患者(15.7%)发生了D-ILD。发生D-ILD的患者组中ILA患者的比例显著高于未发生D-ILD的患者组(分别为9/11(81.8%)对20/59(33.9%),P = 0.0057)。此外,发生D-ILD的患者中磨玻璃影(GGA)和网状影的出现频率更高。发生D-ILD的患者与未发生D-ILD的患者在PFS和OS方面无显著差异(中位PFS分别为8.0(95%置信区间(CI),5.5 - 9.5)个月对5.0(95%CI,4.5 - 5.6)个月,P = 0.11;中位OS分别为未达到(NR)(95%CI,8.7 - NR)对18.2(95%CI,13.2 - NR)个月,P = 0.20)。

结论

在临床实践中接受化疗-免疫检查点抑制剂联合治疗的ES-SCLC患者中,D-ILD的发生率高于临床试验中的发生率。既往有ILA的患者更易发生D-ILD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1559/10562781/e3ca89157500/gr1.jpg

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