Prognostic and Predictive Role of Body Mass Index (BMI) in Metastatic Colorectal Cancer (mCRC): A Pooled Analisys of Tribe and Tribe-2 Studies by GONO.


Journal

Clinical colorectal cancer
ISSN: 1938-0674
Titre abrégé: Clin Colorectal Cancer
Pays: United States
ID NLM: 101120693

Informations de publication

Date de publication:
09 2022
Historique:
received: 15 12 2021
revised: 21 01 2022
accepted: 13 02 2022
pubmed: 20 3 2022
medline: 9 9 2022
entrez: 19 3 2022
Statut: ppublish

Résumé

Obesity is associated with an increased risk of development and recurrence of colorectal cancer. The role of obesity in metastatic colorectal cancer patients (pts) is still unclear, especially in those treated with triplet plus bevacizumab (bev). The aim of our study was to evaluate the prognostic and predictive role of BMI in metastatic colorectal cancer pts treated with FOLFOXIRI plus bev or FOLFIRI/FOLFOX plus bev in the TRIBE and TRIBE-2 trial. A total of 1160 pts enrolled in TRIBE and TRIBE-2 trials were included. Baseline height and weight were used to assign pts to one of the following BMI categories: underweight (group A = BMI <18.5 kg/m In our population, no differences in terms of PFS (P = .43) or OS (P = .99) resulted between 3 groups. No interaction effect between treatment arm and BMI was evident in terms of PFS (Group A HR: 0.65 [95%CI: 0.36-1.16]; Group B HR: 0.77 [95%CI: 0.67-0.88]; Group C HR: 0.67 [95%CI: 0.48-0.93]; P for interaction = .75) or OS (Group A HR: 0.57 [95%CI: 0.29-1.12]; Group B HR: 0.85 [95%CI: 0.73-0.99];Group C HR: 0.69 [95%CI: 0.48-1.01] P for interaction = .36). No statistically significant difference in terms of dose reductions due to toxicities were found according to BMI in the overall population (P = .48) and in pts treated with FOLFOXIRI plus bev (P = .57). BMI was neither prognostic or predictive for PFS and OS in our population. Our analyses showed that the advantage of FOLFOXIRI plus bev versus FOLFIRI/FOLFOX plus bev was independent from BMI.

Sections du résumé

BACKGROUND
Obesity is associated with an increased risk of development and recurrence of colorectal cancer. The role of obesity in metastatic colorectal cancer patients (pts) is still unclear, especially in those treated with triplet plus bevacizumab (bev). The aim of our study was to evaluate the prognostic and predictive role of BMI in metastatic colorectal cancer pts treated with FOLFOXIRI plus bev or FOLFIRI/FOLFOX plus bev in the TRIBE and TRIBE-2 trial.
MATERIALS AND METHODS
A total of 1160 pts enrolled in TRIBE and TRIBE-2 trials were included. Baseline height and weight were used to assign pts to one of the following BMI categories: underweight (group A = BMI <18.5 kg/m
RESULTS
In our population, no differences in terms of PFS (P = .43) or OS (P = .99) resulted between 3 groups. No interaction effect between treatment arm and BMI was evident in terms of PFS (Group A HR: 0.65 [95%CI: 0.36-1.16]; Group B HR: 0.77 [95%CI: 0.67-0.88]; Group C HR: 0.67 [95%CI: 0.48-0.93]; P for interaction = .75) or OS (Group A HR: 0.57 [95%CI: 0.29-1.12]; Group B HR: 0.85 [95%CI: 0.73-0.99];Group C HR: 0.69 [95%CI: 0.48-1.01] P for interaction = .36). No statistically significant difference in terms of dose reductions due to toxicities were found according to BMI in the overall population (P = .48) and in pts treated with FOLFOXIRI plus bev (P = .57).
CONCLUSION
BMI was neither prognostic or predictive for PFS and OS in our population. Our analyses showed that the advantage of FOLFOXIRI plus bev versus FOLFIRI/FOLFOX plus bev was independent from BMI.

Identifiants

pubmed: 35304089
pii: S1533-0028(22)00024-X
doi: 10.1016/j.clcc.2022.02.003
pii:
doi:

Substances chimiques

Organoplatinum Compounds 0
Bevacizumab 2S9ZZM9Q9V
Leucovorin Q573I9DVLP
Fluorouracil U3P01618RT
Camptothecin XT3Z54Z28A

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

220-228

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

Auteurs

Emanuela Dell'Aquila (E)

Department of Medical Oncology, Campus Bio-Medico University of Rome, Rome, Italy; Medical Oncology 1, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Daniele Rossini (D)

Department of Translational Research and New Technologies in Medicine, University of Pisa, Pisa, Italy.

Alessandro Galletti (A)

Department of Medical Oncology, Campus Bio-Medico University of Rome, Rome, Italy.

Marco Stellato (M)

Department of Medical Oncology, Campus Bio-Medico University of Rome, Rome, Italy. Electronic address: m.stellato@unicampus.it.

Alessandra Boccaccino (A)

Department of Translational Research and New Technologies in Medicine, University of Pisa, Pisa, Italy.

Veronica Conca (V)

Department of Translational Research and New Technologies in Medicine, University of Pisa, Pisa, Italy.

Marco Maria Germani (MM)

Department of Translational Research and New Technologies in Medicine, University of Pisa, Pisa, Italy.

Francesca Bergamo (F)

Oncology Unit, Department of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padova, Italy.

Francesca Daniel (F)

Oncology Unit, Department of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padova, Italy.

Andrea Spagnoletti (A)

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Leonardo Provenzano (L)

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Gianluca Tomasello (G)

Division of Medicine and Medical Oncology, Hospital of Cremona, Cremona, Italy.

Alberto Zaniboni (A)

Department of Oncology, Fondazione Poliambulanza Brescia, Brescia, Italy.

Angela Buonadonna (A)

Department of Medical Oncology, Centro di Riferimento Oncologico (CRO), IRCCS, Aviano (PN), Italy.

Laura Fanchini (L)

ColoRectal Cancer Unit-Department of Oncology, AOU Città della Salute e della Scienza di Torino, Torino, Italy.

Samanta Cupini (S)

Department of Oncology, Azienda Toscana Nord Ovest, Division of Medical Oncology, Livorno Hospital, Livorno, Italy.

Chiara Carlomagno (C)

Department of Clinical Medicine and Surgery, University Federico II, Naples, Italy.

Salvatore Caponnetto (S)

Department of Radiological, Oncological and Pathological Science, Sapienza University of Rome, Rome, Italy.

Stefania Rapisardi (S)

Oncology Unit, ARNAS Garibaldi Catania, Catania, Italy.

Daniele Santini (D)

Department of Medical Oncology, Campus Bio-Medico University of Rome, Rome, Italy.

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