Factors Associated With Chemoradiation Therapy Interruption and Noncompletion Among Patients With Squamous Cell Anal Carcinoma.


Journal

JAMA oncology
ISSN: 2374-2445
Titre abrégé: JAMA Oncol
Pays: United States
ID NLM: 101652861

Informations de publication

Date de publication:
01 06 2020
Historique:
pubmed: 24 4 2020
medline: 23 1 2021
entrez: 24 4 2020
Statut: ppublish

Résumé

Definitive chemoradiation for anal cancer is effective but may be associated with toxic effects, and some patients may not be able to complete the planned treatment. Identifying factors associated with treatment interruption and noncompletion is important to target quality improvement efforts. To identify rates of chemoradiation treatment interruption or noncompletion and factors associated with this among patients with anal cancer treated in routine clinical practice. In this population-based, retrospective cohort study, the Ontario Cancer Registry was used to identify all incident cases of squamous cell anal cancer treated with curative-intent radiation from 2007 to 2015 in Ontario, Canada. Final analysis of data was performed on August 9, 2019. Curative-intent radiation therapy. Treatment interruption was defined as more than 7 days between fractions of radiation. Radiation completion was defined as receipt of 45 Gy or more and 25 fractions of radiation. Chemoradiation completion was defined as radiation completion and 2 doses of combination chemotherapy. Associations between patient factors and treatment interruption and noncompletion were estimated with log-binomial models. Cox proportional hazard models were used to estimate the association of treatment interruption or noncompletion with all-cause death, cancer-specific death, and the combined outcome of colostomy or death. Overall, 1125 patients with stage I-III anal cancer were treated with curative-intent radiation. Treatment interruptions occurred in 262 (23%). Radiation and chemoradiation noncompletion occurred in 199 (18%) and 280 (25%), respectively. No associations were found to correlate with an increased risk of treatment interruption. Patients older than 70 years were less likely to complete chemoradiation (risk ratio [RR], 0.60; 95% CI, 0.52-0.70), compared with those younger than 50 years. Patients with a higher number of comorbidities were also less likely to complete chemoradiation (RR, 0.70; 95% CI, 0.51-0.95). Patients who did not complete chemoradiation had a higher risk of requiring salvage abdominoperineal resection (RR, 1.54; 95% CI, 1.03, 2.31), overall death (hazard ratio [HR], 1.54; 95% CI, 1.23-1.92), cancer-specific death (HR, 1.59; 95% CI, 1.14-2.22), and colostomy or death (HR, 1.80; 95% CI: 1.10-2.93). Treatment interruptions longer than 7 days were not associated with death. Many patients undergoing curative-intent chemoradiation for anal cancer experienced treatment interruption or noncompletion. Quality improvement initiatives to optimize treatment continuity and completion are needed.

Identifiants

pubmed: 32324199
pii: 2764903
doi: 10.1001/jamaoncol.2020.0809
pmc: PMC7180731
doi:

Substances chimiques

Antimetabolites, Antineoplastic 0
Fluorouracil U3P01618RT

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

881-887

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

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Auteurs

Michael J Raphael (MJ)

Sunnybrook Health Sciences Centre, Division of Medical Oncology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Division of Cancer Care and Epidemiology, Queen's Cancer Research Institute, Kingston, Ontario, Canada.

Gary Ko (G)

Division of Cancer Care and Epidemiology, Queen's Cancer Research Institute, Kingston, Ontario, Canada.

Christopher M Booth (CM)

Division of Cancer Care and Epidemiology, Queen's Cancer Research Institute, Kingston, Ontario, Canada.
Division of Medical Oncology, Department of Oncology, Queen's University, Kingston, Ontario, Canada.
International Credential Evaluation Service, Queen's, Kingston, Ontario, Canada.

Susan B Brogly (SB)

International Credential Evaluation Service, Queen's, Kingston, Ontario, Canada.
Department of Surgery, Queen's University, Kingston, Ontario, Canada.

Wenbin Li (W)

International Credential Evaluation Service, Queen's, Kingston, Ontario, Canada.

Maria Kalyvas (M)

Division of Cancer Care and Epidemiology, Queen's Cancer Research Institute, Kingston, Ontario, Canada.
Division of Radiation Oncology, Department of Oncology, Queen's University, Kingston, Ontario, Canada.

Timothy P Hanna (TP)

Division of Cancer Care and Epidemiology, Queen's Cancer Research Institute, Kingston, Ontario, Canada.
International Credential Evaluation Service, Queen's, Kingston, Ontario, Canada.
Division of Radiation Oncology, Department of Oncology, Queen's University, Kingston, Ontario, Canada.

Sunil V Patel (SV)

Division of Cancer Care and Epidemiology, Queen's Cancer Research Institute, Kingston, Ontario, Canada.
International Credential Evaluation Service, Queen's, Kingston, Ontario, Canada.
Department of Surgery, Queen's University, Kingston, Ontario, Canada.

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