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在澳大利亚三级肿瘤中心接受免疫检查点抑制剂治疗的晚期非小细胞肺癌、黑色素瘤和肾细胞癌患者的 5 年生存率和临床相关性。

Five-year survival and clinical correlates among patients with advanced non-small cell lung cancer, melanoma and renal cell carcinoma treated with immune check-point inhibitors in Australian tertiary oncology centres.

机构信息

Crown Princess Mary Cancer Centre, Westmead Hospital, Westmead, New South Wales, Australia.

Blacktown Cancer and Haematology Centre, Blacktown Hospital, Blacktown, New South Wales, Australia.

出版信息

Cancer Med. 2023 Mar;12(6):6788-6801. doi: 10.1002/cam4.5468. Epub 2022 Nov 20.

Abstract

AIMS

There is robust trial evidence for improved overall survival (OS) with immunotherapy in advanced solid organ malignancies. The real-world long-term survival data and the predictive variables are not yet known. Our aim was to evaluate factors associated with 3-year and 5-year OS for patients treated with immune checkpoint inhibitors (ICIs).

METHODS

We performed a retrospective study of patients who received ICIs as management of advanced solid organ malignancies in two tertiary Australian oncology centres from 2012-2017. Data pertaining to clinical characteristics, metastatic disease burden, immune-related adverse events (IRAEs) and tumour responses were collected and their relationship to survival examined.

RESULTS

In this analysis of 264 patients, 202 (76.5%) had melanoma, 46 (17.4%) had non-small cell lung cancer (NSCLC), 12 (4.5%) had renal cell carcinoma (RCC) and 4 (1.5%) had mesothelioma. The 5-year OS rates were 42.1% in patients with melanoma, 19.6% with NSCLC, 75% with RCC, and none of the mesothelioma patients were alive at 5 years. In multivariate analysis, an ECOG score of 0 (Hazard ratio [HR] 0.39; 95% confidence interval [CI] 0.23-0.66; p < 0.001) and the occurrence of IRAE's of any grade (HR 0.61; 95% CI 0.37-0.95; p = 0.05) were associated with better 5-year survival. The presence of bone metastases (HR 1.62; 95% CI 1.03-2.82; p = 0.05) and liver metastases (HR 1.76; 95% CI 1.07-2.89; p = 0.03) were associated with worse 5-year survival.

CONCLUSIONS

These results support the long-term benefits of immunotherapy that in some patients, extend to at least 5 years. ECOG performance status of 0 and the occurrence of irAEs are associated with better long-term survival. Survival is significantly influenced by metastatic site and cancer type. These predictive clinical correlates aid discussions and planning in the delivery of ICIs to patients.

摘要

目的

免疫疗法在晚期实体恶性肿瘤中具有显著的总生存期(OS)改善作用,这一结论已经在大量临床试验中得到验证。目前,我们对真实世界中的长期生存数据和预测因素还知之甚少。本研究旨在评估接受免疫检查点抑制剂(ICI)治疗的患者 3 年和 5 年 OS 的相关因素。

方法

我们对 2012 年至 2017 年期间在澳大利亚两家三级肿瘤中心接受 ICI 治疗的晚期实体恶性肿瘤患者进行了回顾性研究。收集了与临床特征、转移性疾病负担、免疫相关不良事件(irAE)和肿瘤反应相关的数据,并对其与生存的关系进行了评估。

结果

本分析共纳入 264 例患者,其中 202 例(76.5%)为黑色素瘤患者,46 例(17.4%)为非小细胞肺癌(NSCLC)患者,12 例(4.5%)为肾细胞癌(RCC)患者,4 例(1.5%)为间皮瘤患者。黑色素瘤患者的 5 年 OS 率为 42.1%,NSCLC 患者为 19.6%,RCC 患者为 75%,间皮瘤患者无一例存活 5 年。多变量分析显示,ECOG 评分为 0(风险比 [HR] 0.39;95%置信区间 [CI] 0.23-0.66;p<0.001)和发生任何级别的 irAE(HR 0.61;95%CI 0.37-0.95;p=0.05)与更好的 5 年生存率相关。骨转移(HR 1.62;95%CI 1.03-2.82;p=0.05)和肝转移(HR 1.76;95%CI 1.07-2.89;p=0.03)与更差的 5 年生存率相关。

结论

这些结果支持免疫治疗的长期获益,在某些患者中,这种获益至少可以持续 5 年。ECOG 表现状态为 0 和发生 irAE 与更好的长期生存相关。生存受转移部位和癌症类型的显著影响。这些预测性临床相关性有助于在向患者提供 ICI 时进行讨论和计划。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b7a/10067054/ee96f5ec6cfb/CAM4-12-6788-g002.jpg

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