Wong Shu Fen, Wong Hui Li, Field Kathryn M, Kosmider Suzanne, Tie Jeanne, Wong Rachel, Tacey Mark, Shapiro Jeremy, Nott Louise, Richardson Gary, Cooray Prasad, Jones Ian, Croxford Matthew, Gibbs Peter
Andrew Love Cancer Centre, University Hospital Geelong, Geelong, VIC, Australia; Deakin University School of Medicine, Waurn Ponds, VIC, Australia.
Department of Medical Oncology, Royal Melbourne Hospital, Parkville, VIC, Australia; Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia; University of Melbourne, Parkville, VIC, Australia.
Clin Colorectal Cancer. 2016 Sep;15(3):e125-32. doi: 10.1016/j.clcc.2015.12.010. Epub 2015 Dec 29.
The survival impact of primary tumor resection in patients with metastatic colorectal cancer (mCRC) treated with palliative intent remains uncertain. In the absence of randomized data, the objectives of the present study were to examine the effect of primary tumor resection (PTR) and major prognostic variables on overall survival (OS) of patients with de novo mCRC.
Consecutive patients from the Australian 'Treatment of Recurrent and Advanced Colorectal Cancer' registry were examined from June 2009 to March 2015. Univariate and multivariate Cox proportional hazards regression analyses were used to identify associations between multiple patient or clinical variables and OS. Patients with metachronous mCRC were excluded from the analyses.
A total of 690 patients de novo and 373 metachronous mCRC patients treated with palliative intent were identified. The median follow-up period was 30 months. The median age of de novo patients was 66 years; 57% were male; 77% had an Eastern Cooperative Oncology Group performance status of 0 to 1; and 76% had a colon primary. A total of 216 de novo mCRC patients treated with palliative intent underwent PTR at diagnosis and were more likely to have a colon primary (odds ratio [OR], 15.4), a lower carcinoembryonic antigen level (OR, 2.08), and peritoneal involvement (OR, 2.58; P < .001). On multivariate analysis, PTR at diagnosis in de novo patients was not associated with significantly improved OS (hazard ratio [HR], 0.82; 99% confidence interval [CI], 0.62-1.09; P = .068). PTR at diagnosis did not correlate with outcome in de novo patients with a colon primary (HR, 0.74; 99% CI, 0.54-1.01; P = .014) or a rectal primary (HR, 0.81; 99% CI, 0.27-2.44; P = .621).
For de novo mCRC patients treated with palliative intent, PTR at diagnosis does not significantly improve OS when adjusting for known major prognostic factors. The outcomes of randomized trials examining the survival impact of PTR are awaited.
对于接受姑息性治疗的转移性结直肠癌(mCRC)患者,原发肿瘤切除对生存的影响仍不确定。在缺乏随机数据的情况下,本研究的目的是探讨原发肿瘤切除(PTR)及主要预后变量对初发性mCRC患者总生存期(OS)的影响。
对2009年6月至2015年3月澳大利亚“复发性和晚期结直肠癌治疗”登记处的连续患者进行研究。采用单因素和多因素Cox比例风险回归分析来确定多个患者或临床变量与OS之间的关联。异时性mCRC患者被排除在分析之外。
共确定了690例初发性和373例接受姑息性治疗的异时性mCRC患者。中位随访期为30个月。初发性患者的中位年龄为66岁;57%为男性;77%的东部肿瘤协作组体能状态为0至1;76%的原发部位在结肠。共有216例接受姑息性治疗的初发性mCRC患者在诊断时接受了PTR,这些患者更有可能原发部位在结肠(比值比[OR],15.4)、癌胚抗原水平较低(OR,2.08)以及有腹膜转移(OR,2.58;P <.001)。多因素分析显示,初发性患者诊断时的PTR与OS的显著改善无关(风险比[HR],0.82;99%置信区间[CI],0.62 - 1.09;P =.068)。诊断时的PTR与原发部位在结肠(HR,0.74;99% CI,0.54 - 1.01;P =.014)或直肠(HR,0.81;99% CI,0.27 - 2.44;P =.621)的初发性患者的预后均无相关性。
对于接受姑息性治疗的初发性mCRC患者,在调整已知的主要预后因素后,诊断时的PTR并不能显著改善OS。期待有关PTR对生存影响的随机试验结果。