Crown Princess Mary Cancer Centre, Westmead Hospital, Westmead, New South Wales, Australia.
Blacktown Cancer and Haematology Centre, Blacktown Hospital, Blacktown, New South Wales, Australia.
Cancer Med. 2023 Mar;12(6):6788-6801. doi: 10.1002/cam4.5468. Epub 2022 Nov 20.
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).
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.
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.
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.
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。
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。
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。
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。