Real-World Treatment and Outcomes of Metastatic Colorectal Cancer Patients With a Poor or Very Poor Performance Status.


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 2021
Historique:
received: 18 06 2020
revised: 05 08 2020
accepted: 09 08 2020
pubmed: 14 9 2020
medline: 15 12 2021
entrez: 13 9 2020
Statut: ppublish

Résumé

The management of metastatic colorectal cancer patients with a poor performance status (PS) continues to be a clinical dilemma, with the potential activity and safety of treating this population remaining poorly understood. Few of these patients are enrolled onto clinical trials, and poor PS is often multifactorial. We analyzed the Treatment of Recurrent and Advanced Colorectal Cancer registry to describe treatment practices and outcomes in poor (Eastern Cooperative Oncology Group [ECOG] PS 2) and very poor PS (ECOG PS > 2) patients to explore the relationship between age, tumor burden, comorbidities, and PS, and to evaluate the benefit of systemic therapy. Standard descriptive statistical methods, Kaplan-Meier analysis, and a multivariate Cox regression model were used. Of 2769 registry patients (diagnosed January 2009 to June 2018), 329 (12%) and 182 (7%) patients had a poor and very poor PS, respectively. Good PS patients were more likely to receive systemic therapy than poor and very poor PS patients (85%, 55%, and 21.5%, P < .0001), but clinician assessed response was observed in all subsets (53%, 41%, and 29%, P = .0003). Treatment with chemotherapy was associated with longer median overall survival across PS groups. Exploratory analysis based on comorbidity score and tumor burden subgroups demonstrated a consistently positive overall survival association with treatment. Benefit was observed where poor overall survival was attributable to medical comorbidities and to tumor burden. In routine clinical care, a substantial proportion of poor and very poor PS patients receive active treatment, which is often associated with meaningful clinical benefit.

Sections du résumé

BACKGROUND
The management of metastatic colorectal cancer patients with a poor performance status (PS) continues to be a clinical dilemma, with the potential activity and safety of treating this population remaining poorly understood. Few of these patients are enrolled onto clinical trials, and poor PS is often multifactorial.
PATIENTS AND METHODS
We analyzed the Treatment of Recurrent and Advanced Colorectal Cancer registry to describe treatment practices and outcomes in poor (Eastern Cooperative Oncology Group [ECOG] PS 2) and very poor PS (ECOG PS > 2) patients to explore the relationship between age, tumor burden, comorbidities, and PS, and to evaluate the benefit of systemic therapy. Standard descriptive statistical methods, Kaplan-Meier analysis, and a multivariate Cox regression model were used.
RESULTS
Of 2769 registry patients (diagnosed January 2009 to June 2018), 329 (12%) and 182 (7%) patients had a poor and very poor PS, respectively. Good PS patients were more likely to receive systemic therapy than poor and very poor PS patients (85%, 55%, and 21.5%, P < .0001), but clinician assessed response was observed in all subsets (53%, 41%, and 29%, P = .0003). Treatment with chemotherapy was associated with longer median overall survival across PS groups. Exploratory analysis based on comorbidity score and tumor burden subgroups demonstrated a consistently positive overall survival association with treatment. Benefit was observed where poor overall survival was attributable to medical comorbidities and to tumor burden.
CONCLUSION
In routine clinical care, a substantial proportion of poor and very poor PS patients receive active treatment, which is often associated with meaningful clinical benefit.

Identifiants

pubmed: 32919889
pii: S1533-0028(20)30106-7
doi: 10.1016/j.clcc.2020.08.002
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e21-e34

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Avraham Travers (A)

Department of Medical Oncology, Calvary Mater Newcastle, Waratah, Australia. Electronic address: Avraham.Travers@calvarymater.org.au.

Azim Jalali (A)

Walter and Eliza Hall Institute of Medical Research, Parkville, Australia; Western Health, Footscray, Australia.

Stephen Begbie (S)

Mid North Coast Cancer Institute, Port Macquarie, Australia.

Christine Semira (C)

Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.

Suzanne Kosmider (S)

Western Health, Footscray, Australia.

Sumitra Ananda (S)

Walter and Eliza Hall Institute of Medical Research, Parkville, Australia; Western Health, Footscray, Australia; Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia; Dentistry and Health Sciences, Faculty of Medicine, University of Melbourne, Parkville, Australia.

Rachel Wong (R)

Walter and Eliza Hall Institute of Medical Research, Parkville, Australia; Eastern Health, Box Hill, Australia; Eastern Health Clinical School, Monash University, Box Hill, Australia; Epworth Healthcare, Box Hill, Australia.

Margaret Lee (M)

Walter and Eliza Hall Institute of Medical Research, Parkville, Australia; Western Health, Footscray, Australia; Eastern Health, Box Hill, Australia; Eastern Health Clinical School, Monash University, Box Hill, Australia.

Jeremy Shapiro (J)

Haematology and Medical Oncology Unit, Cabrini Hospital, Malvern, Australia; Department of Medicine, Monash University, Clayton, Australia.

Matthew Burge (M)

Royal Brisbane and Women's Hospital, Herston, Australia; University of Queensland, St Lucia, Australia.

Desmond Yip (D)

Department of Medical Oncology, Canberra Hospital, Garran, Australia; ANU Medical School, Australian National University, Canberra, Australia.

Javier Torres (J)

Goulburn Valley Health, Shepparton, Australia; Dentistry and Health Sciences-Shepparton Campus, Faculty of Medicine, University of Melbourne, Shepparton, Australia.

Brigette Ma (B)

Chinese University of Hong Kong Prince of Wales Hospital, Department of Clinical Oncology, State Key Laboratory of Translational Oncology, Shatin, New Territories, Hong Kong SAR, China.

Louise Nott (L)

Royal Hobart Hospital, Hobart, Australia.

Andrew Dean (A)

Bendat Cancer Centre, St John of God Subiaco Hospital, Subiaco, Australia.

Jeanne Tie (J)

Walter and Eliza Hall Institute of Medical Research, Parkville, Australia; Western Health, Footscray, Australia; Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia; Dentistry and Health Sciences, Faculty of Medicine, University of Melbourne, Parkville, Australia.

Adnan Khattak (A)

Fiona Stanley Hospital, Murdoch, Australia.

Stephanie Lim (S)

Macarthur Cancer Therapy Centre, Campbelltown Hospital, Campbelltown, Australia.

Hui-Li Wong (HL)

Walter and Eliza Hall Institute of Medical Research, Parkville, Australia; Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.

Peter Gibbs (P)

Walter and Eliza Hall Institute of Medical Research, Parkville, Australia; Western Health, Footscray, Australia.

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Classifications MeSH