Cannone Giorgio, Faccioli Eleonora, Busetto Alberto, Lione Luigi, Maggioni Giuseppe, Nicotra Samuele, Schiavon Marco, Rebusso Alessandro, Comacchio Giovanni, Mammana Marco, Sepulcri Matteo, Pasello Giulia, Calabrese Fiorella, Dell'Amore Andrea, Rea Federico
Thoracic Surgery Unit, Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University Hospital of Padova, 35121 Padova, Italy.
Pathology Unit, Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University Hospital of Padova, 35121 Padova, Italy.
J Clin Med. 2025 Apr 17;14(8):2758. doi: 10.3390/jcm14082758.
: Pancoast tumors are a rare subset of lung cancers that require a multimodal approach (induction chemoradiotherapy and surgery), best performed in highly specialized centers. This study analyzes the outcomes and prognostic factors in patients treated at a high-volume center over an extended period. : We retrospectively reviewed 43 patients who underwent surgery for Pancoast tumors, following induction treatment between 2005 and 2023. Survival was estimated using the Kaplan-Meier method, and a Cox proportional hazards model was applied to identify prognostic factors (significance level = 0.05). : The median patient age was 63 years, with over 90% having a disease at stage III or higher. Induction chemoradiotherapy was administered to 79% of the patients, achieving a pathological complete response (PCR) in 23% of the patients. The median overall survival (OS) was 37 months, with 1-3 and 5-year OS rates of 71%, 52%, and 41%, respectively. The median disease-free survival (DFS) was 38 months, with 1-, 3-, and 5-year DFS rates of 72%, 62%, and 35%, respectively. A pathological complete response (PCR) and vertebral and/or vascular infiltration significantly influenced recurrence and mortality risk. : Trimodal therapy still offers the best short- and long-term outcomes in patients with Pancoast tumors. Future strategies incorporating tyrosine kinase inhibitors and anti-PD1/PD-L1 may improve outcomes for patients by increasing PCR rates and improving disease control.
肺上沟瘤是肺癌中罕见的一种类型,需要采用多模式治疗方法(诱导放化疗和手术),最好在高度专业化的中心进行。本研究分析了在一个大型中心长期接受治疗的患者的治疗结果和预后因素。我们回顾性分析了2005年至2023年间43例接受诱导治疗后进行肺上沟瘤手术的患者。采用Kaplan-Meier法估计生存率,并应用Cox比例风险模型确定预后因素(显著性水平 = 0.05)。患者中位年龄为63岁,超过90%的患者疾病处于III期或更高分期。79%的患者接受了诱导放化疗,其中23%的患者达到了病理完全缓解(PCR)。中位总生存期(OS)为37个月,1年、3年和5年OS率分别为7