Department of Thoracic Surgery and Institute of Thoracic Oncology, West China Hospital, Sichuan University, Chengdu, People's Republic of China.
Int J Surg. 2024 Aug 1;110(8):4617-4623. doi: 10.1097/JS9.0000000000001580.
The most common form of therapy for nonsmall cell lung cancer (NSCLC) in early stage is surgery-based combination therapy, including radiotherapy and immunotherapy. However, postoperative radiotherapy (PORT) of cancer is correlated with increasing risk of second primary malignancy (SPM), especially young-onset cancer cases. The authors aimed to quantify the risks of SPM associated with PORT treatment for young‑onset NSCLC in early stage.
The authors screened for SPM that developed over 5 years since the diagnosis of NSCLC. Using the data from the Surveillance, Epidemiology, and End Results database, PORT-correlated risks were estimated with multivariate Logistic regression analysis. Moreover, Fine-Gray's competing risk regression analysis was used to calculate the cumulative incidence of SPMs.
Among the 30 308 young-onset NSCLC patients in early stage undergoing surgery, a total of 3728 patients have received PORT. Logistic regression analyses showed that PORT showed substantial correlation with elevated risks of second solid malignancies [relative risks (RR)=1.31; 95% CI: 1.17-1.46], lung cancer (RR=1.23; 95% CI: 1.07-1.42), breast cancer (RR=1.74; 95% CI: 1.16-2.74), and colon and rectum cancers (RR=1.37; 95% CI: 1.07-2.06) as well as a negligible risk of second hematologic malignancies (RR=1.15; 95% CI: 0.82-1.67). The cumulative incidence of SPMs revealed similar findings. Higher RR was obtained in NSCLC patients aged 60-69 years (RR=1.33), in white race (RR=1.36), diagnosed in 1975-2000 (RR=1.23) and 2001-2015 (RR=1.40), or diagnosed with lung adenocarcinoma (RR=1.55).
PORT for young-onset NSCLC in early stage was correlated with elevated risks of SPMs (lung cancer, breast cancer, as well as colon and rectum cancers), supporting the need for long-term surveillance of these patients.
非小细胞肺癌(NSCLC)早期最常见的治疗形式是基于手术的联合治疗,包括放疗和免疫治疗。然而,癌症术后放疗(PORT)与第二原发恶性肿瘤(SPM)的风险增加相关,尤其是年轻发病的癌症病例。作者旨在量化早期年轻 NSCLC 患者接受 PORT 治疗后 SPM 的风险。
作者筛选了自 NSCLC 诊断以来 5 年内发生的 SPM。利用监测、流行病学和最终结果数据库的数据,采用多变量 Logistic 回归分析估计 PORT 相关风险。此外,采用 Fine-Gray 竞争风险回归分析计算 SPM 的累积发生率。
在 30308 名早期接受手术的年轻 NSCLC 患者中,共有 3728 名患者接受了 PORT。Logistic 回归分析表明,PORT 与第二实体恶性肿瘤(RR=1.31;95%CI:1.17-1.46)、肺癌(RR=1.23;95%CI:1.07-1.42)、乳腺癌(RR=1.74;95%CI:1.16-2.74)、结肠和直肠癌症(RR=1.37;95%CI:1.07-2.06)的风险显著增加相关,而第二血液恶性肿瘤(RR=1.15;95%CI:0.82-1.67)的风险可忽略不计。SPM 的累积发生率也显示出类似的发现。60-69 岁的 NSCLC 患者(RR=1.33)、白人(RR=1.36)、1975-2000 年诊断(RR=1.23)和 2001-2015 年诊断(RR=1.40)或诊断为肺腺癌(RR=1.55)的患者,RR 值更高。
早期年轻 NSCLC 患者接受 PORT 治疗与 SPM(肺癌、乳腺癌以及结肠和直肠癌症)风险增加相关,支持对这些患者进行长期监测。