Small Cell Lung Cancer

JAMA Pub Date : 2025-03-31 DOI:10.1001/jama.2025.0560
So Yeon Kim, Henry S. Park, Anne C. Chiang
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Abstract

ImportanceSmall cell lung cancer (SCLC) is a high-grade neuroendocrine carcinoma with an incidence of 4.7 cases per 100 000 individuals in 2021 in the US and a 5-year overall survival of 12% to 30%.ObservationsCigarette smoking is the primary risk factor for development of SCLC, as 95% of patients diagnosed with SCLC have a history of tobacco use. Patients with SCLC may present with respiratory symptoms such as cough (40%), shortness of breath (34%), hemoptysis (10%), or metastases with corresponding local symptoms (30%) such as pleuritis or bone pain; approximately 60% of patients with SCLC may be asymptomatic at diagnosis. Chest imaging may demonstrate central hilar (85%) or mediastinal lymphadenopathy (75%). At diagnosis, approximately 15% of patients have brain metastases, which may present as headache or focal weakness. Diagnosis is confirmed by biopsy of a primary lung mass, thoracic lymph node, or metastatic lesion. Small cell lung cancer is classified into limited stage (LS-SCLC; 30%) vs extensive stage (ES-SCLC; 70%) based on whether the disease can be treated within a radiation field that is typically confined to 1 hemithorax but may include contralateral mediastinal and supraclavicular nodes. For patients with LS-SCLC, surgery or concurrent chemotherapy with platinum-etoposide and radiotherapy is potentially curative in 30% of patients. More recently, median survival for LS-SCLC has reached up to 55.9 months with the addition of durvalumab, an immunotherapy. First-line treatment for ES-SCLC is combined treatment with platinum-etoposide chemotherapy and immunotherapy with the programmed cell death 1 ligand 1 (PD-L1) inhibitors durvalumab or atezolizumab followed by maintenance immunotherapy until disease progression or toxicity. Although initial rates of tumor shrinkage are 60% to 70% with platinum-etoposide and immunotherapy treatment, the median overall survival of patients treated for ES-SCLC is approximately 12 to 13 months, with 60% of patients relapsing within 3 months. Second-line therapy for patients with ES-SCLC includes the DNA-alkylating agent lurbinectedin (35% overall response rate; median progression-free survival, 3.7 months) and a bispecific T-cell engager against delta-like ligand 3, tarlatamab (40% overall response rate; median progression-free survival, 4.9 months).Conclusions and RelevanceSmall cell lung cancer is a smoking-related malignancy that presents at an advanced stage in 70% of patients. Three-year overall survival is approximately 56.5% for LS-SCLC and 17.6% for ES-SCLC. First-line treatment for LS-SCLC is radiation targeting the tumor given concurrently with chemotherapy and followed by consolidation immunotherapy. For ES-SCLC, first-line treatment is chemotherapy and immunotherapy followed by maintenance immunotherapy.
小细胞肺癌
小细胞肺癌(SCLC)是一种高级神经内分泌癌,2021年在美国的发病率为每10万人4.7例,5年总生存率为12%至30%。吸烟是SCLC发生的主要危险因素,95%被诊断为SCLC的患者有吸烟史。SCLC患者可能表现为呼吸道症状,如咳嗽(40%)、呼吸短促(34%)、咯血(10%),或转移灶伴有相应的局部症状(30%),如胸膜炎或骨痛;大约60%的SCLC患者在诊断时可能无症状。胸部影像学可显示肺门中央(85%)或纵隔淋巴结病变(75%)。诊断时,约15%的患者出现脑转移,表现为头痛或局灶性虚弱。诊断可通过肺原发肿块、胸淋巴结或转移性病变的活检来证实。小细胞肺癌分为有限期(LS-SCLC;30%) vs广泛期(ES-SCLC;70%),基于该疾病是否可以在典型局限于半胸的放射场内治疗,但可能包括对侧纵隔淋巴结和锁骨上淋巴结。对于LS-SCLC患者,30%的患者手术或铂-依托泊苷联合化疗和放疗可能治愈。最近,随着durvalumab(一种免疫疗法)的加入,LS-SCLC的中位生存期已达到55.9个月。ES-SCLC的一线治疗是联合铂-依托泊苷化疗和免疫治疗与程序性细胞死亡1配体1 (PD-L1)抑制剂durvalumab或atezolizumab,然后维持免疫治疗,直到疾病进展或毒性。虽然初始肿瘤收缩率在铂-依托泊苷和免疫疗法治疗下为60% - 70%,但ES-SCLC患者的中位总生存期约为12 - 13个月,60%的患者在3个月内复发。ES-SCLC患者的二线治疗包括dna烷基化剂lurbinectedin(总有效率35%;中位无进展生存期,3.7个月)和针对δ样配体3的双特异性t细胞接合剂tarlatamab(总有效率40%;中位无进展生存期,4.9个月)。小细胞肺癌是一种与吸烟相关的恶性肿瘤,70%的患者出现在晚期。LS-SCLC的三年总生存率约为56.5%,ES-SCLC为17.6%。LS-SCLC的一线治疗是放射靶向肿瘤,同时给予化疗,然后进行巩固免疫治疗。对于ES-SCLC,一线治疗是化疗和免疫治疗,然后是维持免疫治疗。
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