Tumor-associated Macrophages as Prognostic and Predictive Biomarkers for Postoperative Adjuvant Chemotherapy in Patients with Stage II Colon Cancer

被引:115
作者
Feng, Qingyang [1 ,2 ]
Chang, Wenju [1 ,2 ]
Mao, Yihao [1 ,2 ]
He, Guodong [1 ,2 ]
Zheng, Peng [1 ,2 ]
Tang, Wentao [1 ,2 ]
Wei, Ye [1 ,2 ]
Ren, Li [1 ,2 ]
Zhu, Dexiang [1 ,2 ]
Ji, Meiling [1 ,2 ]
Tu, Yongjiu [3 ]
Qin, Xinyu [1 ,2 ]
Xu, Jianmin [1 ,2 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Gen Surg Dept, Shanghai, Peoples R China
[2] Shanghai Engn Res Ctr Colorectal Canc Minimally I, Shanghai, Peoples R China
[3] 174th Hosp PLA, Xiamen, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
COLORECTAL-CANCER; IMPROVED SURVIVAL; MISMATCH REPAIR; FLUOROURACIL; EXPRESSION; IMMUNOHISTOCHEMISTRY; INFILTRATION; OUTCOMES; THERAPY; BENEFIT;
D O I
10.1158/1078-0432.CCR-18-2076
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: For stage II colon cancer, the efficacy of postoperative adjuvant chemotherapy remains controversial. It is well known that tumor-associated macrophages (TAMs) are important in tumor progression. In this study, TAMs were investigated as prognostic and predictive biomarkers for the efficacy of adjuvant chemotherapy for stage II colon cancer after radical resection. Experimental Design: This study enrolled two independent cohorts of consecutive patients from one medical center with pathologic stage II colon cancer after radical resections. Macro-phages were detected using IHC staining of CD68 and CD206. Infiltration densities of CD68(+) TAMs, CD206(+) TAMs, and ratio of CD206(+) TAMs/CD68(+) TAMs (CD206/CD68 ratio) were calculated as prognostic and predictive biomarkers. Results: The primary and validation cohorts consisted of 521 and 314 patients, respectively. In both cohorts, high CD206/CD68 ratio was significantly associated with poor disease-free survival (DFS) and overall survival (OS). As an independent risk factor, CD206/CD68 ratio also had significantly better prognostic efficacy than CD68(+) TAM density, CD206(+) TAM density, and traditional clinicopathologic highrisk factors. Moreover, adjuvant chemotherapy significantly improved DFS and OS for patients with high CD206/CD68 ratio but not for those with low CD206/CD68 ratio. The interaction analyses were also significant for DFS. In subgroup analysis, CD206/CD68 ratio was still a significant predictor for adjuvant chemotherapy for patients in traditional high-risk group of recurrence (significant interaction for DFS). Conclusions: For stage II colon cancer, CD206/CD68 ratio is a better prognostic and predictive biomarker for postoperative adjuvant chemotherapy. Together with clinicopathologic high-risk factors, it will aid in precision treatment.
引用
收藏
页码:3896 / 3907
页数:12
相关论文
共 42 条
[1]   Adjuvant Fluorouracil, Leucovorin, and Oxaliplatin in Stage II to III Colon Cancer: Updated 10-Year Survival and Outcomes According to BRAF Mutation and Mismatch Repair Status of the MOSAIC Study [J].
Andre, Thierry ;
de Gramont, Armand ;
Vernerey, Dewi ;
Chibaudel, Benoist ;
Bonnetain, Franck ;
Tijeras-Raballand, Annemilai ;
Scriva, Aurelie ;
Hickish, Tamas ;
Tabernero, Josep ;
Van Laethem, Jean Luc ;
Banzi, Maria ;
Maartense, Eduard ;
Shmueli, Einat ;
Carlsson, Goran U. ;
Scheithauer, Werner ;
Papamichael, Demetris ;
Moeehler, Marcus ;
Landolfi, Stefania ;
Demetter, Pieter ;
Colote, Soudhir ;
Tournigand, Christophe ;
Louvet, Christophe ;
Duval, Alex ;
Flejou, Jean-Francois ;
de Gramont, Aimery .
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (35) :4176-+
[2]  
[Anonymous], 2018, Clinical Practice Guidelines in Oncology: Antiemesis
[3]   Reflex Immunohistochemistry and Microsatellite Instability Testing of Colorectal Tumors for Lynch Syndrome Among US Cancer Programs and Follow-Up of Abnormal Results [J].
Beamer, Laura C. ;
Grant, Marcia L. ;
Espenschied, Carin R. ;
Blazer, Kathleen R. ;
Hampel, Heather L. ;
Weitzel, Jeffrey N. ;
MacDonald, Deborah J. .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (10) :1058-1063
[4]   Macrophage plasticity and interaction with lymphocyte subsets: cancer as a paradigm [J].
Biswas, Subhra K. ;
Mantovani, Alberto .
NATURE IMMUNOLOGY, 2010, 11 (10) :889-896
[5]   Risk of recurrence in patients with colon cancer stage II and III: A systematic review and meta-analysis of recent literature [J].
Bockelman, Camilla ;
Engelmann, Bodil E. ;
Kaprio, Tuomas ;
Hansen, Torben F. ;
Glimelius, Bengt .
ACTA ONCOLOGICA, 2015, 54 (01) :5-16
[6]   Intratumoral macrophages contribute to epithelial-mesenchymal transition in solid tumors [J].
Bonde, Anne-Katrine ;
Tischler, Verena ;
Kumar, Sushil ;
Soltermann, Alex ;
Schwendener, Reto A. .
BMC CANCER, 2012, 12
[7]   X-tile: A new bio-informatics tool for biomarker assessment and outcome-based cut-point optimization [J].
Camp, RL ;
Dolled-Filhart, M ;
Rimm, DL .
CLINICAL CANCER RESEARCH, 2004, 10 (21) :7252-7259
[8]   Adjuvant Chemotherapy Is Associated With Improved Survival in Patients With Stage II Colon Cancer [J].
Casadaban, Leigh ;
Rauscher, Garth ;
Aklilu, Mebea ;
Villenes, Dana ;
Freels, Sally ;
Maker, Ajay V. .
CANCER, 2016, 122 (21) :3277-3287
[9]   Macrophages: Obligate partners for tumor cell migration, invasion, and metastasis [J].
Condeelis, J ;
Pollard, JW .
CELL, 2006, 124 (02) :263-266
[10]   Mutant p53 cancers reprogram macrophages to tumor supporting macrophages via exosomal miR-1246 [J].
Cooks, Tomer ;
Pateras, Ioannis S. ;
Jenkins, Lisa M. ;
Patel, Keval M. ;
Robles, Ana I. ;
Morris, James ;
Forshew, Tim ;
Appella, Ettore ;
Gorgoulis, Vassilis G. ;
Harris, Curtis C. .
NATURE COMMUNICATIONS, 2018, 9