Clinical impact of first-line bevacizumab plus chemotherapy in metastatic colorectal cancer of mucinous histology: a multicenter, retrospective analysis on 685 patients

被引:7
作者
Catalano, Vincenzo [1 ]
Bergamo, Francesca [2 ]
Cremolini, Chiara [3 ]
Vincenzi, Bruno [4 ]
Negri, Francesca [5 ]
Giordani, Paolo [1 ]
Alessandroni, Paolo [1 ]
Intini, Rossana [2 ]
Stragliotto, Silvia [2 ]
Rossini, Daniele [3 ]
Borelli, Beatrice [3 ]
Santini, Daniele [4 ]
Sarti, Donatella [1 ]
Rocchi, Marco B. L. [6 ]
Lonardi, Sara [2 ]
Falcone, Alfredo [3 ]
Zagonel, Vittorina [2 ]
Mattioli, Rodolfo [1 ]
Graziano, Francesco [1 ]
机构
[1] Azienda Osped Osped Riuniti Marche Nord, Dept Oncol, Via Lombroso 1, I-61122 Pesaro, Italy
[2] IRCCS, Ist Oncol Veneto, Dept Clin & Expt Oncol, Med Oncol Unit 1, Padua, Italy
[3] Univ Pisa, Azienda Osped Univ Pisana, Dept Translat Res & New Technol Med, Unit Med Oncol, Pisa, Italy
[4] Campus Biomed Univ Roma, Dept Med Oncol, Rome, Italy
[5] Osped Univ, Dept Oncol, Parma, Italy
[6] Univ Carlo Bo, Dept Biomol Sci, Unita Stat Med & Biometria, Urbino, Italy
关键词
Metastatic colorectal cancer; Mucinous histology; Chemotherapy; Bevacizumab; MOLECULAR SUBTYPES; CARCINOMA; COLON; IRINOTECAN; PREDICTS; SURVIVAL; OUTCOMES; ADENOCARCINOMA; OXALIPLATIN; EXPRESSION;
D O I
10.1007/s00432-019-03077-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeIn metastatic colorectal cancer (MCRC), mucinous histology has been associated with poor response rate and prognosis. We investigated whether bevacizumab combined with different chemotherapy regimens may have an impact on clinical outcomes of MCRC patients with mucinous histology.Methods685 MCRC patients were classified in mucinous adenocarcinoma (MC) and non-mucinous adenocarcinoma (NMC) and were treated with first-line bevacizumab plus fluoropyrimidine (FP)-based, oxaliplatin (OXA)-based, irinotecan (IRI)-based, or FOLFOXIRI.ResultsNinety-four (13.7%) patients had MC. With a median follow-up of 50 months, MC patients had a median overall survival (OS) of 28.2 months compared with 27.7 months for the NMC group [hazard ratio (HR)=0.92; 95% confidence interval (CI) 0.70-1.19, P=0.530]. The overall response rates for MC and NMC were 41.5% (95% CI 31.5-51.4) and 62.4% (95% CI 58.4-66.3), respectively (Chi-square test, P<0.003). After correcting for significant prognostic factors by multivariate Cox regression analysis, age, resection of the primary tumour, and number of metastatic sites were found to be associated with poorer OS, but not mucinous histology.ConclusionCompared with NMC, MCRC patients with mucinous histology treated with bevacizumab plus chemotherapy had comparable OS despite lower overall response rate.
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收藏
页码:493 / 501
页数:9
相关论文
共 32 条
[1]   Mucinous histology predicts for poor response rate and overall survival of patients with colorectal cancer and treated with first-line oxaliplatin- and/or irinotecan-based chemotherapy [J].
Catalano, V. ;
Loupakis, F. ;
Graziano, F. ;
Torresi, U. ;
Bisonni, R. ;
Mari, D. ;
Fornaro, L. ;
Baldelli, A. M. ;
Giordani, P. ;
Rossi, D. ;
Alessandroni, P. ;
Giustini, L. ;
Silva, R. R. ;
Falcone, A. ;
D'Emidio, S. ;
Fedeli, S. L. .
BRITISH JOURNAL OF CANCER, 2009, 100 (06) :881-887
[2]  
Consorti F, 2000, J SURG ONCOL, V73, P70, DOI 10.1002/(SICI)1096-9098(200002)73:2<70::AID-JSO3>3.0.CO
[3]  
2-J
[4]   Molecular subtypes of metastatic colorectal cancer are associated with patient response to irinotecan-based therapies [J].
Del Rio, M. ;
Mollevi, C. ;
Bibeau, F. ;
Vie, N. ;
Selves, J. ;
Emile, J. -F. ;
Roger, P. ;
Gongora, C. ;
Robert, J. ;
Tubiana-Mathieu, N. ;
Ychou, M. ;
Martineau, P. .
EUROPEAN JOURNAL OF CANCER, 2017, 76 :68-75
[5]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247
[6]   Discovery and development of bevacizumab, an anti-VEGF antibody for treating cancer [J].
Ferrara, N ;
Hillan, KJ ;
Gerber, HP ;
Novotny, W .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (05) :391-400
[7]   Unfavourable expression of pharmacologic markers in mucinous colorectal cancer [J].
Glasgow, SC ;
Yu, J ;
Carvalho, LP ;
Shannon, WD ;
Fleshman, JW ;
McLeod, HL .
BRITISH JOURNAL OF CANCER, 2005, 92 (02) :259-264
[8]   MUCINOUS CARCINOMA - JUST ANOTHER COLON CANCER [J].
GREEN, JB ;
TIMMCKE, AE ;
MITCHELL, WT ;
HICKS, TC ;
GATHRIGHT, JB ;
RAY, JE .
DISEASES OF THE COLON & RECTUM, 1993, 36 (01) :49-54
[9]   The consensus molecular subtypes of colorectal cancer [J].
Guinney, Justin ;
Dienstmann, Rodrigo ;
Wang, Xin ;
de Reynies, Aurelien ;
Schlicker, Andreas ;
Soneson, Charlotte ;
Marisa, Laetitia ;
Roepman, Paul ;
Nyamundanda, Gift ;
Angelino, Paolo ;
Bot, Brian M. ;
Morris, Jeffrey S. ;
Simon, Iris M. ;
Gerster, Sarah ;
Fessler, Evelyn ;
Melo, Felipe De Sousa E. ;
Missiaglia, Edoardo ;
Ramay, Hena ;
Barras, David ;
Homicsko, Krisztian ;
Maru, Dipen ;
Manyam, Ganiraju C. ;
Broom, Bradley ;
Boige, Valerie ;
Perez-Villamil, Beatriz ;
Laderas, Ted ;
Salazar, Ramon ;
Gray, Joe W. ;
Hanahan, Douglas ;
Tabernero, Josep ;
Bernards, Rene ;
Friend, Stephen H. ;
Laurent-Puig, Pierre ;
Medema, Jan Paul ;
Sadanandam, Anguraj ;
Wessels, Lodewyk ;
Delorenzi, Mauro ;
Kopetz, Scott ;
Vermeulen, Louis ;
Tejpar, Sabine .
NATURE MEDICINE, 2015, 21 (11) :1350-1356
[10]   Advances in the care of patients with mucinous colorectal cancer [J].
Hugen, Niek ;
Brown, Gina ;
Glynne-Jones, Robert ;
de Wilt, Johannes H. W. ;
Nagtegaal, Iris D. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2016, 13 (06) :361-369