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Cetuximab versus bevacizumab in metastatic colorectal cancer: a comparative effectiveness study.
Marques, Rui Pedro; Godinho, Ana Rita; Heudtlass, Peter; Pais, Helena Luna; Quintela, António; Martins, Ana Paula.
Affiliation
  • Marques RP; Faculty of Pharmacy, University of Lisbon, Avenida Professor Gama Pinto, 1649-003, Lisbon, Portugal. rui.p.marques@chln.min-saude.pt.
  • Godinho AR; Hospital de Santa Maria, Centro Hospitalar Universitário de Lisboa Norte (CHULN), Lisbon, Portugal. rui.p.marques@chln.min-saude.pt.
  • Heudtlass P; Centre for Health Evaluation & Research (CEFAR), Portuguese Pharmacy Association (ANF), Lisbon, Portugal.
  • Pais HL; Centre for Health Evaluation & Research (CEFAR), Portuguese Pharmacy Association (ANF), Lisbon, Portugal.
  • Quintela A; Hospital de Santa Maria, Centro Hospitalar Universitário de Lisboa Norte (CHULN), Lisbon, Portugal.
  • Martins AP; Hospital de Santa Maria, Centro Hospitalar Universitário de Lisboa Norte (CHULN), Lisbon, Portugal.
J Cancer Res Clin Oncol ; 146(5): 1321-1334, 2020 May.
Article de En | MEDLINE | ID: mdl-32144533
ABSTRACT

PURPOSE:

Uncertainty exists regarding comparative effectiveness of cetuximab versus bevacizumab in metastatic colorectal cancer (mCRC). We conducted a retrospective head-to-head multi-cohort study comparing clinical outcomes from both antibodies

METHODS:

Cohorts were defined by treatment line and subgroups by (K)RAS status and tumour sidedness. Among other outcomes, we estimated and compared response rates, progression-free (PFS) and overall survival (OS).

RESULTS:

Between January 2010 and April 2018, 311 patients were included. Except for (K)RAS mutation status, baseline characteristics were balanced across treatment groups. In the full analysis of first and second-line cohorts, PFS (first-line HR = 0.85; 95% CI 0.64 to 1.13; P = 0.26; second-line HR = 1.16; 95% CI 0.74 to 1.83; P = 0.51) and OS (first-line HR = 0.83; 95% CI 0.61 to 1.15; P = 0.26; second-line HR = 0.88; 95% CI 0.56 to 1.38; P = 0.58) were similar between bevacizumab and cetuximab arms. In subgroup analyses of first-line therapy, we found a survival difference favouring bevacizumab in right-sided tumours (PFS HR = 0.52; 95% CI 0.29 to 0.93; P = 0.025; OS HR = 0.60; 95% CI 0.32 to 1.12; P = 0.11), but not in left-sided (HR = 1.04; 95% CI 0.75 to 1.46; P = 0.81; OS HR = 0.94; 95% CI 0.65 to 1.36; P = 0.74), or (K)RAS wild-type tumours (PFS HR = 0.91; 95% CI 0.60 to 1.40; P = 0.67; OS HR = 0.79; 95% CI 0.50 to 1.25; P = 0.31). Response rates were similar across treatment groups, except for the subgroup of patients bearing right-sided primaries, where bevacizumab performed substantially better.

CONCLUSION:

This study provides evidence suggesting bevacizumab and cetuximab lead to similar effectiveness outcomes in mCRC, except for right-sided tumours, where cetuximab seemed to show considerably poorer outcomes. Further research is needed to confirm these results.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs du rectum / Tumeurs du côlon / Bévacizumab / Cétuximab / Antinéoplasiques immunologiques Type d'étude: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limites: Aged / Female / Humans / Male / Middle aged Langue: En Journal: J Cancer Res Clin Oncol Année: 2020 Type de document: Article Pays d'affiliation: Portugal

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs du rectum / Tumeurs du côlon / Bévacizumab / Cétuximab / Antinéoplasiques immunologiques Type d'étude: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limites: Aged / Female / Humans / Male / Middle aged Langue: En Journal: J Cancer Res Clin Oncol Année: 2020 Type de document: Article Pays d'affiliation: Portugal