Josephides Eleni, Dunn Roberta, Henry Annie-Rose, Pilling John, Harrison-Phipps Karen, Patel Akshay, Ahmad Shahreen, Skwarski Michael, Spicer James, Georgiou Alexandros, Ghosh Sharmistha, Van Hemelrijck Mieke, Karapanagiotou Eleni, Smith Daniel, Bille Andrea
Guy's and St Thomas' NHS Foundation Trust, London SE1 9RT, UK.
Comprehensive Cancer Centre, King's College, London SE1 9RT, UK.
Cancers (Basel). 2024 Sep 2;16(17):3058. doi: 10.3390/cancers16173058.
Stage IIIA-N2 non-small cell lung cancer (NSCLC) poses a significant clinical challenge, with low survival rates despite advances in therapy. The lack of a standardised treatment approach complicates patient management. This study utilises real-world data from Guy's Thoracic Cancer Database to analyse patient outcomes, identify key predictors of overall survival (OS) and disease-free survival (DFS), and address the limitations of randomised controlled trials.
This observational, single-centre, non-randomised study analysed 142 patients diagnosed with clinical and pathological T1/2 N2 NSCLC who received curative treatment from 2015 to 2021. Patients were categorised into three groups: Group A (30 patients) underwent surgery for clinical N2 disease, Group B (54 patients) had unsuspected N2 disease discovered during surgery, and Group C (58 patients) received radical chemoradiation or radiotherapy alone (CRT/RT) for clinical N2 disease. Data on demographics, treatment types, recurrence, and survival rates were analysed.
The median OS for the cohort was 31 months, with 2-year and 5-year OS rates of 60% and 30%, respectively. Group A had a median OS of 32 months, Group B 36 months, and Group C 25 months. The median DFS was 18 months overall, with Group A at 16 months, Group B at 22 months, and Group C at 17 months. Significant predictors of OS included ECOG performance status, lymphovascular invasion, and histology. No significant differences in OS were found between treatment groups ( = 0.99).
This study highlights the complexity and diversity of Stage IIIA-N2 NSCLC, with no single superior treatment strategy identified. The findings underscore the necessity for personalised treatment approaches and multidisciplinary decision-making. Future research should focus on integrating newer therapeutic modalities and conducting multi-centre trials to refine treatment strategies. Collaboration and ongoing data collection are crucial for improving personalised treatment plans and survival outcomes for Stage IIIA-N2 NSCLC patients.
IIIA-N2期非小细胞肺癌(NSCLC)带来了重大的临床挑战,尽管治疗取得了进展,但生存率仍然较低。缺乏标准化的治疗方法使患者管理变得复杂。本研究利用盖伊胸科癌症数据库的真实世界数据来分析患者预后,确定总生存期(OS)和无病生存期(DFS)的关键预测因素,并解决随机对照试验的局限性。
这项观察性、单中心、非随机研究分析了142例在2015年至2021年期间接受根治性治疗的临床和病理诊断为T1/2 N2 NSCLC的患者。患者分为三组:A组(30例患者)对临床N2期疾病进行了手术,B组(54例患者)在手术期间发现了意外的N2期疾病,C组(58例患者)对临床N2期疾病接受了根治性放化疗或单纯放疗(CRT/RT)。分析了人口统计学、治疗类型、复发和生存率的数据。
该队列的中位OS为31个月,2年和5年OS率分别为60%和30%。A组的中位OS为32个月,B组为36个月,C组为25个月。总体中位DFS为18个月,A组为16个月,B组为22个月,C组为17个月。OS的显著预测因素包括东部肿瘤协作组(ECOG)体能状态、脉管侵犯和组织学。治疗组之间的OS没有显著差异(=0.99)。
本研究突出了IIIA-N2期NSCLC的复杂性和多样性,未发现单一的优越治疗策略。研究结果强调了个性化治疗方法和多学科决策的必要性。未来的研究应专注于整合更新的治疗模式并开展多中心试验以完善治疗策略。合作和持续的数据收集对于改善IIIA-N2期NSCLC患者的个性化治疗方案和生存结局至关重要。