Qiu Yiwen, Cao Nida, Meng Dan, Yuan Jian, Zhu Yingjie
Department of Oncology, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Sci Rep. 2025 Feb 3;15(1):4045. doi: 10.1038/s41598-025-88555-7.
Given concerns about treatment, there is uncertainty surrounding the effect of prior malignancy on the survival of individuals with metastatic colorectal cancer. This study sought to evaluate how prior malignancy impacts the survival of patients with metastatic colorectal cancer (mCRC). Patients diagnosed with stage IV mCRC (per the American Joint Committee on Cancer [AJCC] 6th edition) between 2004 and 2015 were identified from the Surveillance, Epidemiology, and End Results (SEER) database. Those without a prior history of malignancy were assigned to the control group, whereas those with a prior history of malignancy were assigned to the research group. Propensity score matching (PSM) was utilized to ensure that the baseline characteristics were balanced. The Kaplan‒Meier method was used for survival analysis, as were the multivariate Cox proportional hazard model and multivariate competing risk model. The PSM analysis included 54365 eligible patients with mCRC. Among them, 4,845 (8.9%) had a history of prior malignancy. A history of prior malignancy was associated with a greater cancer-specific survival rate (adjusted hazard ratio (AHR) ) = 0.49; 95% CI [0.47-0.51]). Subgroup analyses revealed that a prior diagnosis of a skin tumour (AHR = 1.37; 95% CI [1.11-1.69]) and a history of prior malignancy of more than five years (AHR = 1.39; 95% CI [1.23-1.57]) had adverse effects on the clinical outcomes of patients with mCRC. Our findings suggest that patients with a prior malignancy diagnosis may experience prolonged survival. Subgroup analysis indicated that a malignancy diagnosed more than 5 years ago may adversely impact the clinical outcomes of patients with mCRC. Therefore, we advocate for active standardized treatment for these patients and propose expanding the range of prior malignancies included in clinical trials based on publication timelines, primary tumour locations, and genetic testing results. The objective is to facilitate timely and proactive treatment for patients following the disclosure of results, thereby instilling confidence in the management of mCRC.
鉴于对治疗的担忧,既往恶性肿瘤对转移性结直肠癌患者生存的影响存在不确定性。本研究旨在评估既往恶性肿瘤如何影响转移性结直肠癌(mCRC)患者的生存。从监测、流行病学和最终结果(SEER)数据库中识别出2004年至2015年间被诊断为IV期mCRC(根据美国癌症联合委员会[AJCC]第6版)的患者。无既往恶性肿瘤病史的患者被分配到对照组,而有既往恶性肿瘤病史的患者被分配到研究组。采用倾向评分匹配(PSM)来确保基线特征平衡。采用Kaplan-Meier方法进行生存分析,同时使用多变量Cox比例风险模型和多变量竞争风险模型。PSM分析纳入了54365例符合条件的mCRC患者。其中,4845例(8.9%)有既往恶性肿瘤病史。既往恶性肿瘤病史与更高的癌症特异性生存率相关(调整后风险比[AHR]=0.49;95%置信区间[0.47-0.51])。亚组分析显示,既往诊断为皮肤肿瘤(AHR=1.37;95%置信区间[1.11-1.69])和既往恶性肿瘤病史超过五年(AHR=1.39;95%置信区间[1.23-1.57])对mCRC患者的临床结局有不利影响。我们的研究结果表明,有既往恶性肿瘤诊断的患者可能生存期延长。亚组分析表明,5年多前诊断的恶性肿瘤可能对mCRC患者的临床结局产生不利影响。因此,我们主张对这些患者进行积极的标准化治疗,并建议根据发表时间、原发肿瘤位置和基因检测结果扩大临床试验中既往恶性肿瘤的范围。目的是在结果披露后为患者提供及时、积极的治疗,从而增强对mCRC管理的信心。