Dawe David E, Rittberg Rebekah, Syed Iqra, Shanahan Mary Kate, Moldaver Daniel, Bucher Oliver, Galloway Katie, Reynolds Kayla, Paul James T, Harlos Craig, Kim Julian O, Banerji Shantanu
Department of Internal Medicine, University of Manitoba, Winnipeg, MB, Canada.
Department of Hematology and Medical Oncology, CancerCare Manitoba, Winnipeg, MB, Canada.
Front Oncol. 2023 Sep 18;13:1191855. doi: 10.3389/fonc.2023.1191855. eCollection 2023.
Extensive-stage small-cell lung cancer (ES-SCLC) is an incurable cancer with poor prognosis in which characteristics predictive of long-term survival are debated. The utility of agents such as immune checkpoint inhibitors highlights the importance of identifying key characteristics and treatment strategies that contribute to long-term survival and could help guide therapeutic decisions.
This real-world analysis examines the characteristics, treatment patterns, and clinical outcomes of patients receiving chemotherapy without immunotherapy for ES-SCLC in Manitoba, Canada.
A retrospective cohort study assessed patient characteristics, treatment, and survival duration (short: <6 months; medium: 6-24 months; long: >24 months) using the Manitoba Cancer Registry and CancerCare Manitoba records. Eligible patients were aged >18 years with cytologically confirmed ES-SCLC diagnosed between January 1, 2004, and December 31, 2018, and received cytotoxic chemotherapy (CT). The one-, two-, and five-year probabilities of overall survival (OS) were assessed relative to patient, disease, and treatment characteristics using Kaplan-Meier methods and Cox proportional hazards models.
This analysis included 537 patients. Cisplatin was used in 56.1% of patients, 45.6% received thoracic radiotherapy (RT), and few received prophylactic cranial irradiation (PCI). In the overall cohort, one-, two- and five-year OS rates were 26%, 8%, and 3%, respectively. For patients with Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0, OS rates at one, two, and five years were 43%, 17%, and 10%, respectively, vs. 27%, 8%, and 2% for those with ECOG PS 1-2, and 16%, 3%, and 3% for those with ECOG PS 3-4. In long-term survivors, ECOG PS scores were lower and abnormal laboratory test results were less frequent. Overall, 74.4% of long-term survivors received thoracic RT and 53.5% received PCI. Known poor prognostic factors - including brain/liver metastases, high lactate dehydrogenase (LDH), abnormal sodium, and low hemoglobin levels - were less common but still seen in long-term survivors.
Although rare, patients with ES-SCLC may experience long-term survival with CT ± thoracic RT ± PCI. Factors predicting long-term survival include traditional prognostic factors such as ECOG PS, LDH level, and receipt of thoracic RT or PCI. These findings support current treatment algorithms for ES-SCLC and provide baseline survival estimates to assess the real-world impact of adding immune checkpoint inhibitors in the future.
广泛期小细胞肺癌(ES-SCLC)是一种无法治愈、预后较差的癌症,关于其长期生存预测特征存在争议。免疫检查点抑制剂等药物的应用凸显了识别有助于长期生存并能指导治疗决策的关键特征和治疗策略的重要性。
本真实世界分析考察了加拿大曼尼托巴省接受不含免疫疗法的化疗的ES-SCLC患者的特征、治疗模式和临床结局。
一项回顾性队列研究使用曼尼托巴癌症登记处和曼尼托巴癌症护理记录评估患者特征、治疗和生存时长(短:<6个月;中:6 - 24个月;长:>24个月)。符合条件的患者年龄>18岁,2004年1月1日至2018年12月31日期间经细胞学确诊为ES-SCLC,并接受了细胞毒性化疗(CT)。使用Kaplan-Meier方法和Cox比例风险模型评估相对于患者、疾病和治疗特征的1年、2年和5年总生存(OS)概率。
该分析纳入了537例患者。56.1%的患者使用了顺铂,45.6%接受了胸部放疗(RT),很少有人接受预防性脑照射(PCI)。在整个队列中,1年、2年和5年的OS率分别为26%、8%和3%。东部肿瘤协作组体能状态(ECOG PS)为0的患者,1年、2年和5年的OS率分别为43%、17%和10%,而ECOG PS为1 - 2的患者分别为27%、8%和2%,ECOG PS为3 - 4的患者分别为16%、3%和3%。长期生存者的ECOG PS评分较低,实验室检查结果异常的频率较低。总体而言,74.4%的长期生存者接受了胸部放疗,53.5%接受了PCI。已知的不良预后因素——包括脑/肝转移、高乳酸脱氢酶(LDH)、血钠异常和血红蛋白水平低——较少见,但在长期生存者中仍可见到。
尽管罕见,但ES-SCLC患者通过CT±胸部放疗±PCI可能实现长期生存。预测长期生存的因素包括传统预后因素,如ECOG PS、LDH水平以及是否接受胸部放疗或PCI。这些发现支持当前ES-SCLC的治疗算法,并提供基线生存估计,以评估未来添加免疫检查点抑制剂的真实世界影响。