Disease-Free Survival and Time to Complete Response After Definitive Chemoradiotherapy for Squamous-Cell Carcinoma of the Anus According to HIV Infection.


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 2020
Historique:
received: 28 12 2019
revised: 18 03 2020
accepted: 22 03 2020
pubmed: 12 5 2020
medline: 7 9 2021
entrez: 12 5 2020
Statut: ppublish

Résumé

The standard treatment for localized squamous-cell carcinoma of the anal canal is definitive chemoradiotherapy. A meta-analysis of published studies conducted by our group showed significantly lower rates of disease-free survival (DFS) and overall survival at 3 years among HIV-positive patients. We aimed to compare detailed treatment outcomes between the groups of HIV-positive and -negative patients. We performed a retrospective multicenter study of a comparative cohort of consecutive patients with histologic diagnosis of localized squamous-cell carcinoma of the anal canal who received definitive chemoradiotherapy. Patients' characteristics and outcomes were compared according to HIV status. The primary end points were time to complete response (CR) and DFS time. From June 2001 to September 2018, a total of 185 patients were included; 43 (30.2%) were HIV positive and 142 (69.8%) were HIV negative. The overall CR rates were 67.4% and 91.5% for HIV-positive and -negative patients, respectively (P < .001). The median follow-up was 47.8 months and the median time to experience CR was 7.8 months (95% confidence interval [CI], 5.7-10.5) for HIV-positive versus 4.89 months (95% CI, 4.54-5.25) for HIV-negative (P < .001) patients. The median DFS times were 79.7 months (95% CI, 56.8-102.6) and 127.9 months (95% CI, 112.6-143.2) for HIV-positive and -negative patients, respectively (P = .02). There was a trend toward greater grade 3/4 toxicity in the HIV-positive group. HIV-positive patients take longer to experience CR and present worse DFS. These findings have clinical implications because waiting longer to define CR among these patients may prevent unnecessary anorectal amputations.

Sections du résumé

BACKGROUND
The standard treatment for localized squamous-cell carcinoma of the anal canal is definitive chemoradiotherapy. A meta-analysis of published studies conducted by our group showed significantly lower rates of disease-free survival (DFS) and overall survival at 3 years among HIV-positive patients. We aimed to compare detailed treatment outcomes between the groups of HIV-positive and -negative patients.
PATIENTS AND METHODS
We performed a retrospective multicenter study of a comparative cohort of consecutive patients with histologic diagnosis of localized squamous-cell carcinoma of the anal canal who received definitive chemoradiotherapy. Patients' characteristics and outcomes were compared according to HIV status. The primary end points were time to complete response (CR) and DFS time.
RESULTS
From June 2001 to September 2018, a total of 185 patients were included; 43 (30.2%) were HIV positive and 142 (69.8%) were HIV negative. The overall CR rates were 67.4% and 91.5% for HIV-positive and -negative patients, respectively (P < .001). The median follow-up was 47.8 months and the median time to experience CR was 7.8 months (95% confidence interval [CI], 5.7-10.5) for HIV-positive versus 4.89 months (95% CI, 4.54-5.25) for HIV-negative (P < .001) patients. The median DFS times were 79.7 months (95% CI, 56.8-102.6) and 127.9 months (95% CI, 112.6-143.2) for HIV-positive and -negative patients, respectively (P = .02). There was a trend toward greater grade 3/4 toxicity in the HIV-positive group.
CONCLUSION
HIV-positive patients take longer to experience CR and present worse DFS. These findings have clinical implications because waiting longer to define CR among these patients may prevent unnecessary anorectal amputations.

Identifiants

pubmed: 32389596
pii: S1533-0028(20)30043-8
doi: 10.1016/j.clcc.2020.03.006
pii:
doi:

Types de publication

Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e129-e136

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.

Auteurs

Marcos Pedro Guedes Camandaroba (MPG)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil.

Soledad Iseas (S)

Department of Clinical Oncology, Bonorino Udaondo Hospital, Buenos Aires, Argentina.

Caroline Oliveira (C)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil.

Rodrigo G Taboada (RG)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil.

Mariana P Xerfan (MP)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil.

Carine C Mauro (CC)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil.

Virgilio S Silva (VS)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil.

Milton Barros (M)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil.

Victor Hugo F de Jesus (VHF)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil.

Tiago Felismino (T)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil.

Samuel Aguiar (S)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil.

Maria Leticia Gobo (ML)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil.

Celso A Mello (CA)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil.

Rachel P Riechelmann (RP)

Department of Clinical Oncology, AC. Camargo Cancer Center, São Paulo, Brazil. Electronic address: Rachel.riechelmann@accamargo.org.br.

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