Right versus left sided metastatic colorectal cancer: Teasing out clinicopathologic drivers of disparity in survival

被引:16
作者
Mendis, Shehara [1 ]
Beck, Sophie [2 ]
Lee, Belinda [2 ,3 ,4 ]
Lee, Margaret [1 ,2 ,3 ,4 ,5 ]
Wong, Rachel [2 ,5 ,6 ]
Kosmider, Suzanne [1 ]
Shapiro, Jeremy [7 ]
Yip, Desmond [8 ,9 ,10 ]
Steel, Simone [11 ]
Nott, Louise [12 ]
Jennens, Ross [13 ]
Lipton, Lara [1 ,7 ]
Burge, Matthew [14 ]
Field, Kathryn [3 ,4 ]
Ananda, Sumitra [1 ]
Wong, Hui-Li [2 ]
Gibbs, Peter [1 ,2 ,3 ,4 ,15 ]
机构
[1] Footscray Hosp, Western Hlth, 160 Gordon St, Footscray, Vic 3011, Australia
[2] Walter & Eliza Hall Inst Med Res, Parkville, Vic, Australia
[3] Royal Melbourne Hosp, Parkville, Vic, Australia
[4] Univ Melbourne, Fac Med & Hlth Sci, Melbourne, Vic, Australia
[5] Box Hill Hosp, Eastern Hlth, Box Hill, Vic, Australia
[6] Monash Univ, Fac Nursing & Hlth Sci, Clayton, Vic, Australia
[7] Cabrini Hlth, Malvern, Vic, Australia
[8] Canberra Hosp, Garran, ACT, Australia
[9] Calvary Hosp, Garran, ACT, Australia
[10] Canberra Hosp, ANU Med Sch, Garran, ACT, Australia
[11] Peninsula Private Hosp, Frankston, Vic, Australia
[12] Royal Hobart Hosp, Hobart, Tas, Australia
[13] Epworth Med Fdn, Richmond, Vic, Australia
[14] Royal Brisbane Hosp, Herston, Qld, Australia
[15] BioGrid Australia, Melbourne, Vic, Australia
关键词
colonic neoplasms; multivariate analysis; proportional hazards models; rectal neoplasms; registries; MISMATCH REPAIR STATUS; PRIMARY TUMOR SITE; COLON-CANCER; BRAF MUTATION; BEVACIZUMAB; CHEMOTHERAPY; IMPACT; CETUXIMAB; BENEFIT; FLUOROURACIL;
D O I
10.1111/ajco.13135
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Metastatic colorectal cancer (mCRC) patients with a right-sided primary (RC) have an inferior survival to mCRC arising from a left-sided primary (LC). Previous analyses have suggested multiple factors contribute. Methods The Treatment of Recurrent and Advanced Colorectal Cancer (TRACC) Registry prospectively captured data on consecutive mCRC patients. RC were defined as tumors proximal to the splenic flexure; LC were those at and distal to the splenic flexure and included rectal cancers. Patient, tumor, treatment, and survival data were analyzed stratified by side. Results Of 2306 patients enrolled from July 2009-March 2018, 747 (32%) had an RC. Patients with RC were older, more likely to be female and have a Charlson score >= 3. RC were more frequently BRAF mutated, deficient in mismatch repair, associated with peritoneal metastases, and less likely to receive chemotherapy. Progression-free survival on first-line systemic therapy was inferior for RC patients (8.1 vs. 10.8 months, hazard ratio [HR] for progression in RC 1.38, P < 0.001). Median overall survival for all RC patients was inferior (19.6 vs. 27.5 months, HR for death in RC 1.44, P < 0.001), and inferior within the treated (21 vs. 29.5 months, HR 1.52, P < 0.001) and untreated subgroups (5.9 vs. 10.3 months, HR 1.38, P = 0.009). Primary side remained a significant factor for overall survival in multivariate analysis. Conclusion Our data from a real-world population confirms the poorer prognosis associated with RC. Primary tumor location remains significantly associated with overall survival even when adjusting for multiple factors, indicating the existence of further side-based differences that are as yet undefined.
引用
收藏
页码:136 / 143
页数:8
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