Patterns of Use, Safety, and Effectiveness of Targeted Therapies in First-Line Treatment of Metastatic Colorectal Cancer According to Age: The STROMBOLI Cohort Study.


Journal

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

Informations de publication

Date de publication:
03 2019
Historique:
received: 17 05 2018
revised: 20 11 2018
accepted: 21 11 2018
pubmed: 12 1 2019
medline: 20 7 2019
entrez: 12 1 2019
Statut: ppublish

Résumé

Metastatic colorectal cancer (mCRC) is increasingly treated using targeted therapies. Their real-life evaluation is insufficient, especially in elderly and frail patients. The aim was to describe use, safety, and effectiveness of targeted therapies in first-line mCRC treatment according to age. Two field cohorts of patients initiating bevacizumab or cetuximab for first-line mCRC were pooled. Patients characteristics, use, and safety were compared between younger and elderly patients (<75 vs. ≥75 years). Two-year overall survival (OS) and progression-free survival (PFS) were estimated in both age groups using the Kaplan-Meier method adjusted on factors associated with death or progression identified with Cox multivariate modeling. Eight hundred patients (n = 411, 51.4% bevacizumab) were included: 498 (62.3%) male, median age 64 years, 118 (14.8%) Eastern Cooperative Oncology Group performance status (ECOG-PS) ≥2. Elderly patients (n = 126, 15.8%) were more often treated with 5-fluorouracil alone than younger. Severe adverse events were equivalent across age groups. ECOG-PS ≥1, abnormal hemoglobin, and abnormal alkaline phosphatases were associated with a higher risk of death; OS adjusted on these factors was similar between elderly and younger patients. ECOG-PS ≥1, lung metastases, abnormal hemoglobin, and abnormal creatinine clearance were associated with a higher risk of progression or death; PFS adjusted on these factors was similar across groups. Despite treatment adaptations, elderly patients could benefit from targeted therapies as younger without safety warning.

Sections du résumé

BACKGROUND
Metastatic colorectal cancer (mCRC) is increasingly treated using targeted therapies. Their real-life evaluation is insufficient, especially in elderly and frail patients. The aim was to describe use, safety, and effectiveness of targeted therapies in first-line mCRC treatment according to age.
PATIENTS AND METHODS
Two field cohorts of patients initiating bevacizumab or cetuximab for first-line mCRC were pooled. Patients characteristics, use, and safety were compared between younger and elderly patients (<75 vs. ≥75 years). Two-year overall survival (OS) and progression-free survival (PFS) were estimated in both age groups using the Kaplan-Meier method adjusted on factors associated with death or progression identified with Cox multivariate modeling.
RESULTS
Eight hundred patients (n = 411, 51.4% bevacizumab) were included: 498 (62.3%) male, median age 64 years, 118 (14.8%) Eastern Cooperative Oncology Group performance status (ECOG-PS) ≥2. Elderly patients (n = 126, 15.8%) were more often treated with 5-fluorouracil alone than younger. Severe adverse events were equivalent across age groups. ECOG-PS ≥1, abnormal hemoglobin, and abnormal alkaline phosphatases were associated with a higher risk of death; OS adjusted on these factors was similar between elderly and younger patients. ECOG-PS ≥1, lung metastases, abnormal hemoglobin, and abnormal creatinine clearance were associated with a higher risk of progression or death; PFS adjusted on these factors was similar across groups.
CONCLUSION
Despite treatment adaptations, elderly patients could benefit from targeted therapies as younger without safety warning.

Identifiants

pubmed: 30630730
pii: S1533-0028(18)30247-0
doi: 10.1016/j.clcc.2018.11.005
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Bevacizumab 2S9ZZM9Q9V
Cetuximab PQX0D8J21J
Fluorouracil U3P01618RT

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e150-e162

Investigateurs

D Smith (D)
N Tubiana-Mathieu (N)
P Michel (P)
R Guimbaud (R)
Y Becouarn (Y)
F Viret (F)
R Guimbaud (R)
D Larregain-Fournier (D)
Y Botreau (Y)
P Texereau (P)
D Auby (D)
L Gautier-Felizot (L)
I Loury-Larivière (I)
E Brudieux (E)
L Cany (L)
C Lecaille (C)
D Jaubert (D)
P Guichard (P)
O Bernard (O)
L Vives (L)
N Taoubi (N)
M Martinez (M)
F Burki (F)
I Roque (I)
F Thouveny (F)
M H Gaspard (MH)

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Amandine Gouverneur (A)

Univ Bordeaux, Inserm, Bordeaux Population Health Research Center, Team Pharmacoepidemiology, UMR 1219, Bordeaux, France; Bordeaux PharmacoEpi, INSERM CIC1401, Bordeaux, France; CHU de Bordeaux, Pôle de Sante publique, Service de Pharmacologie médicale, Bordeaux, France. Electronic address: amandine.gouverneur@u-bordeaux.fr.

Juliette Coutureau (J)

Univ Bordeaux, Inserm, Bordeaux Population Health Research Center, Team Pharmacoepidemiology, UMR 1219, Bordeaux, France; CHU de Bordeaux, Pôle de Sante publique, Service de Pharmacologie médicale, Bordeaux, France.

Jérémy Jové (J)

Bordeaux PharmacoEpi, INSERM CIC1401, Bordeaux, France; ADERA, Pessac, France.

Magali Rouyer (M)

Bordeaux PharmacoEpi, INSERM CIC1401, Bordeaux, France; ADERA, Pessac, France.

Angela Grelaud (A)

Bordeaux PharmacoEpi, INSERM CIC1401, Bordeaux, France; ADERA, Pessac, France.

Sophie Duc (S)

Service de Gériatrie, CHU Bordeaux, Bordeaux, France.

Stéphane Gérard (S)

Service de Gériatrie, CHU Toulouse, Toulouse, France.

Denis Smith (D)

Service d'Oncologie médicale, CHU Bordeaux, Bordeaux, France.

Alain Ravaud (A)

Service d'Oncologie médicale, CHU Bordeaux, Bordeaux, France.

Cécile Droz (C)

Bordeaux PharmacoEpi, INSERM CIC1401, Bordeaux, France; ADERA, Pessac, France.

Marie-Agnès Bernard (MA)

Bordeaux PharmacoEpi, INSERM CIC1401, Bordeaux, France; ADERA, Pessac, France.

Régis Lassalle (R)

Bordeaux PharmacoEpi, INSERM CIC1401, Bordeaux, France; ADERA, Pessac, France.

Annie Forrier-Réglat (A)

Univ Bordeaux, Inserm, Bordeaux Population Health Research Center, Team Pharmacoepidemiology, UMR 1219, Bordeaux, France; Bordeaux PharmacoEpi, INSERM CIC1401, Bordeaux, France; CHU de Bordeaux, Pôle de Sante publique, Service de Pharmacologie médicale, Bordeaux, France.

Pernelle Noize (P)

Univ Bordeaux, Inserm, Bordeaux Population Health Research Center, Team Pharmacoepidemiology, UMR 1219, Bordeaux, France; Bordeaux PharmacoEpi, INSERM CIC1401, Bordeaux, France; CHU de Bordeaux, Pôle de Sante publique, Service de Pharmacologie médicale, Bordeaux, France.

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