Chemotherapy and biologic use in the routine management of metastatic colorectal cancer in Australia: is clinical practice following the evidence?


Journal

Internal medicine journal
ISSN: 1445-5994
Titre abrégé: Intern Med J
Pays: Australia
ID NLM: 101092952

Informations de publication

Date de publication:
04 2019
Historique:
received: 03 07 2018
revised: 28 08 2018
accepted: 30 08 2018
pubmed: 20 9 2018
medline: 9 1 2020
entrez: 20 9 2018
Statut: ppublish

Résumé

Emerging evidence on the optimal use of chemotherapy and biologics in patients with metastatic colorectal cancer should impact management in routine care. Recent studies have demonstrated benefits for initial triplet chemotherapy (5-fluorouracil, oxaliplatin and irinotecan, FOLFOXIRI) and for initial treatment with an epidermal growth factor receptor inhibitor (EGFRi) in patients with a RAS wild-type tumour and a left-sided primary tumour. To explore evolving pattern of metastatic colorectal cancer care over time in Australia. We analysed data from the Treatment of Recurrent and Advanced Colorectal Cancer registry. From July 2009 to December 2017, 2552 metastatic colorectal cancer patients were entered into the Treatment of Recurrent and Advanced Colorectal Cancer registry. Of 1585 patients who initially underwent chemotherapy, treatment was with a doublet in 76%. FOLFOXIRI was given to 22 patients (1.4%), mostly young patients and those with potentially resectable disease. Along with first-line chemotherapy, 61% received bevacizumab, while 3.3% received an EGFRi, predominantly over the last 2 years. Within the KRAS wild-type left-sided tumour cohort, EGFRi use increased from 9% in 2015 to 37% in 2017. Across treatment sites, there was a wide variation in the utilisation of FOLFOXIRI and EGFRi therapy; bevacizumab use was more consistent. A clear impact on survival outcomes from these regimens is not evident, potentially due to multiple confounders. Doublet chemotherapy + bevacizumab remains the dominant initial strategy, with limited uptake of triplet chemotherapy and of EGFRi. Potential explanations include uncertainty about the significance of post hoc analyses for EGFRi and concerns regarding adverse events for both strategies.

Sections du résumé

BACKGROUND
Emerging evidence on the optimal use of chemotherapy and biologics in patients with metastatic colorectal cancer should impact management in routine care. Recent studies have demonstrated benefits for initial triplet chemotherapy (5-fluorouracil, oxaliplatin and irinotecan, FOLFOXIRI) and for initial treatment with an epidermal growth factor receptor inhibitor (EGFRi) in patients with a RAS wild-type tumour and a left-sided primary tumour.
AIM
To explore evolving pattern of metastatic colorectal cancer care over time in Australia.
METHODS
We analysed data from the Treatment of Recurrent and Advanced Colorectal Cancer registry.
RESULTS
From July 2009 to December 2017, 2552 metastatic colorectal cancer patients were entered into the Treatment of Recurrent and Advanced Colorectal Cancer registry. Of 1585 patients who initially underwent chemotherapy, treatment was with a doublet in 76%. FOLFOXIRI was given to 22 patients (1.4%), mostly young patients and those with potentially resectable disease. Along with first-line chemotherapy, 61% received bevacizumab, while 3.3% received an EGFRi, predominantly over the last 2 years. Within the KRAS wild-type left-sided tumour cohort, EGFRi use increased from 9% in 2015 to 37% in 2017. Across treatment sites, there was a wide variation in the utilisation of FOLFOXIRI and EGFRi therapy; bevacizumab use was more consistent. A clear impact on survival outcomes from these regimens is not evident, potentially due to multiple confounders.
CONCLUSION
Doublet chemotherapy + bevacizumab remains the dominant initial strategy, with limited uptake of triplet chemotherapy and of EGFRi. Potential explanations include uncertainty about the significance of post hoc analyses for EGFRi and concerns regarding adverse events for both strategies.

Identifiants

pubmed: 30230679
doi: 10.1111/imj.14115
doi:

Substances chimiques

Angiogenesis Inhibitors 0
Biological Products 0
Organoplatinum Compounds 0
Bevacizumab 2S9ZZM9Q9V
Leucovorin Q573I9DVLP
Fluorouracil U3P01618RT

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

446-454

Subventions

Organisme : Roche Products Pty Limited (Australia)
Pays : International

Informations de copyright

© 2018 Royal Australasian College of Physicians.

Auteurs

Christine Semira (C)

Systems Biology and Personalised Medicine Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia.

Hui-Li Wong (HL)

Systems Biology and Personalised Medicine Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia.

Kathryn Field (K)

Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia.
Department of Medical Oncology, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.

Margaret Lee (M)

Systems Biology and Personalised Medicine Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia.
Department of Medical Oncology, Western Health, Melbourne, Victoria, Australia.
Department of Medical Oncology, Eastern Health, Melbourne, Victoria, Australia.

Belinda Lee (B)

Systems Biology and Personalised Medicine Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia.

Louise Nott (L)

Department of Medical Oncology, Royal Hobart Hospital, Hobart, Tasmania, Australia.

Jeremy Shapiro (J)

Department of Medical Oncology, Cabrini Health, Melbourne, Victoria, Australia.

Rachel Wong (R)

Systems Biology and Personalised Medicine Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia.
Department of Medical Oncology, Eastern Health, Melbourne, Victoria, Australia.

Jeanne Tie (J)

Systems Biology and Personalised Medicine Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia.
Department of Medical Oncology, Western Health, Melbourne, Victoria, Australia.
Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.

Ben Tran (B)

Systems Biology and Personalised Medicine Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia.
Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.

Gary Richardson (G)

Department of Medical Oncology, Cabrini Health, Melbourne, Victoria, Australia.

Allan Zimet (A)

Department of Medical Oncology, Epworth Hospital, Melbourne, Victoria, Australia.

Lara Lipton (L)

Department of Medical Oncology, Cabrini Health, Melbourne, Victoria, Australia.

Babak Tamjid (B)

Department of Medical Oncology, Goulburn Valley Health, Shepparton, Victoria, Australia.

Matthew Burge (M)

Department of Medical Oncology, Royal Brisbane Hospital, Brisbane, Queensland, Australia.

Brigette Ma (B)

Department of Clinical Oncology, Prince of Wales Hospital, Chinese University of Hong Kong, Sha Tin, Hong Kong.

Julie Johns (J)

Systems Biology and Personalised Medicine Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.

Michael Harold (M)

Systems Biology and Personalised Medicine Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.

Peter Gibbs (P)

Systems Biology and Personalised Medicine Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia.
Department of Medical Oncology, Western Health, Melbourne, Victoria, Australia.

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