Qi Yana, Sun Yulan, Hu Yanran, Zhu Hui, Guo Hongbo
Department of Radiation OncologyShandong Cancer Hospital and InstituteShandong Academy of Medical Sciences, Shandong First Medical University, 440 Jiyan Road, Jinan, 250117, Shandong Province, China.
Department of Medical OncologyShandong Cancer Hospital and InstituteShandong Academy of Medical Sciences, Shandong First Medical University, 440 Jiyan Road, Jinan, 250117, Shandong Province, China.
Sci Rep. 2025 May 26;15(1):18422. doi: 10.1038/s41598-025-99571-y.
Neoadjuvant chemoimmunotherapy has been successfully used in patients with resectable non-small-cell lung cancer (NSCLC). However, its application to potentially resectable IIIA/IIIB NSCLC remains controversial. This retrospective study aims to evaluate the efficacy and safety of neoadjuvant chemoimmunotherapy followed by conversion surgery in patients with potentially resectable stage III NSCLC, focusing on conversion rate and survival benefits. Patients with 'potentially resectable' stage IIIA/IIIB NSCLC who were deemed unsuitable for complete (R0) resection at initial diagnosis were retrospectively identified. After 2-4 cycles of treatment, all patients were reevaluated for surgical resectability. Data on patient characteristics, radiological and pathological responses, and survival outcomes were collected. In total, 148 patients were included in the final analysis. Upon the completion of neoadjuvant therapy, 105 patients were considered suitable for conversion surgery. Three patients refused surgery, and 102 patients ultimately underwent surgery, yielding a conversion rate of 70.9% and a resection rate of 68.9%. The rate of complete (R0) resection was 100%, with a major pathological response (MPR) of 64.7% and a pathologic complete response (pCR) of 41.2%. Postoperative complications were observed in nine patients (8.8%), and there was no surgery-related mortality within 30 days. The median progression-free survival (PFS) was 19.1 months in the non-surgery group, and the overall survival (OS) was not reached. In the 102 patients who underwent conversion surgery, both the median PFS and OS were not reached, accompanied by 2-year OS and PFS rates of 87.3% and 78.4%, respectively. Our findings showed that neoadjuvant chemoimmunotherapy expanded the opportunities for conversion surgery in potentially resectable cases. Subsequent conversion surgery is safe and has the potential for significant survival benefits.
新辅助化疗免疫疗法已成功应用于可切除的非小细胞肺癌(NSCLC)患者。然而,其在潜在可切除的IIIA/IIIB期NSCLC中的应用仍存在争议。这项回顾性研究旨在评估新辅助化疗免疫疗法联合转化手术在潜在可切除的III期NSCLC患者中的疗效和安全性,重点关注转化率和生存获益。回顾性纳入了初诊时被认为不适合进行根治性(R0)切除的“潜在可切除”IIIA/IIIB期NSCLC患者。经过2-4个周期的治疗后,对所有患者重新评估手术可切除性。收集了患者特征、影像学和病理反应以及生存结果的数据。最终分析共纳入148例患者。新辅助治疗完成后,105例患者被认为适合进行转化手术。3例患者拒绝手术,102例患者最终接受了手术,转化率为70.9%,切除率为68.9%。根治性(R0)切除率为100%,主要病理反应(MPR)为64.7%,病理完全缓解(pCR)为41.2%。9例患者(8.8%)出现术后并发症,30天内无手术相关死亡。非手术组的中位无进展生存期(PFS)为19.1个月,总生存期(OS)未达到。在接受转化手术的102例患者中,中位PFS和OS均未达到,2年OS率和PFS率分别为87.3%和78.4%。我们的研究结果表明,新辅助化疗免疫疗法扩大了潜在可切除病例中转化手术的机会。后续的转化手术是安全的,并且有可能带来显著的生存获益。