The association between protease inhibitors and anal cancer outcomes in veterans living with HIV treated with definitive chemoradiation: a retrospective study.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
05 Jul 2021
Historique:
received: 14 09 2020
accepted: 15 06 2021
entrez: 6 7 2021
pubmed: 7 7 2021
medline: 3 11 2021
Statut: epublish

Résumé

The incidence of anal squamous cell carcinoma has been increasing, particularly in people living with HIV (PLWH). There is concern that radiosensitizing drugs, such as protease inhibitors, commonly used in the management of HIV, may increase toxicities in patients undergoing chemoradiation. This study examines treatment outcomes and toxicities in PLWH managed with and without protease inhibitors who are receiving chemoradiation for anal cancer. Patient demographic, HIV management, and cancer treatment information were extracted from multiple Veterans Affairs databases. Patients were also manually chart reviewed. Among PLWH undergoing chemoradiation for anal carcinoma, therapy outcomes and toxicities were compared between those treated with and without protease inhibitors at time of cancer treatment. Statistical analysis was performed using chi-square, Cox regression analysis, and logistic regression. A total of 219 PLWH taking anti-retroviral therapy undergoing chemoradiation for anal cancer were identified and included in the final analysis. The use of protease inhibitors was not associated with any survival outcome including colostomy-free survival, progression-free survival, or overall survival (all adjusted hazard ratio p-values> 0.05). Regarding toxicity, protease inhibitor use was not associated with an increased odds of hospitalizations or non-hematologic toxicities; however, protease inhibitor use was associated with increased hospitalizations for hematologic toxicities, including febrile neutropenia (p < 0.01). The use of protease inhibitors during chemoradiation for anal carcinoma was not associated with any clinical outcome or increase in non-hematologic toxicity. Their use was associated with increased hospitalizations for hematologic toxicities. Further prospective research is needed to evaluate the safety and efficacy of protease inhibitors for patients undergoing chemoradiation.

Sections du résumé

BACKGROUND BACKGROUND
The incidence of anal squamous cell carcinoma has been increasing, particularly in people living with HIV (PLWH). There is concern that radiosensitizing drugs, such as protease inhibitors, commonly used in the management of HIV, may increase toxicities in patients undergoing chemoradiation. This study examines treatment outcomes and toxicities in PLWH managed with and without protease inhibitors who are receiving chemoradiation for anal cancer.
METHODS METHODS
Patient demographic, HIV management, and cancer treatment information were extracted from multiple Veterans Affairs databases. Patients were also manually chart reviewed. Among PLWH undergoing chemoradiation for anal carcinoma, therapy outcomes and toxicities were compared between those treated with and without protease inhibitors at time of cancer treatment. Statistical analysis was performed using chi-square, Cox regression analysis, and logistic regression.
RESULTS RESULTS
A total of 219 PLWH taking anti-retroviral therapy undergoing chemoradiation for anal cancer were identified and included in the final analysis. The use of protease inhibitors was not associated with any survival outcome including colostomy-free survival, progression-free survival, or overall survival (all adjusted hazard ratio p-values> 0.05). Regarding toxicity, protease inhibitor use was not associated with an increased odds of hospitalizations or non-hematologic toxicities; however, protease inhibitor use was associated with increased hospitalizations for hematologic toxicities, including febrile neutropenia (p < 0.01).
CONCLUSION CONCLUSIONS
The use of protease inhibitors during chemoradiation for anal carcinoma was not associated with any clinical outcome or increase in non-hematologic toxicity. Their use was associated with increased hospitalizations for hematologic toxicities. Further prospective research is needed to evaluate the safety and efficacy of protease inhibitors for patients undergoing chemoradiation.

Identifiants

pubmed: 34225709
doi: 10.1186/s12885-021-08514-z
pii: 10.1186/s12885-021-08514-z
pmc: PMC8256603
doi:

Substances chimiques

Protease Inhibitors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

776

Subventions

Organisme : Dan L. Duncan Cancer Center, Baylor College of Medicine
ID : P30CA022453
Organisme : BLRD VA
ID : I01 BX004420
Pays : United States
Organisme : U.S. Department of Veterans Affairs
ID : CX001430
Organisme : CSRD VA
ID : I01 CX001430
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA206476
Pays : United States
Organisme : U.S. Department of Veterans Affairs
ID : CIN13-413
Organisme : NIH HHS
ID : R01CA206476
Pays : United States

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Auteurs

Alison K Yoder (AK)

University of Texas Health Science Center at Houston, McGovern School of Medicine, Houston, TX, USA.
Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

David S Lakomy (DS)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Dartmouth College Geisel School of Medicine, Hanover, NH, USA.

Yongquan Dong (Y)

Department of Medicine, Baylor College of Medicine, 1155 Pressler St. Unit, Houston, 1340, USA.
Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, USA.

Suchismita Raychaudhury (S)

Department of Medicine, Baylor College of Medicine, 1155 Pressler St. Unit, Houston, 1340, USA.
Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, USA.

Kathryn Royse (K)

Department of Medicine, Baylor College of Medicine, 1155 Pressler St. Unit, Houston, 1340, USA.

Christine Hartman (C)

Department of Medicine, Baylor College of Medicine, 1155 Pressler St. Unit, Houston, 1340, USA.
Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, USA.

Peter Richardson (P)

Department of Medicine, Baylor College of Medicine, 1155 Pressler St. Unit, Houston, 1340, USA.
Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, USA.

Donna L White (DL)

Department of Medicine, Baylor College of Medicine, 1155 Pressler St. Unit, Houston, 1340, USA.
Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, USA.

Jennifer R Kramer (JR)

Department of Medicine, Baylor College of Medicine, 1155 Pressler St. Unit, Houston, 1340, USA.
Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, USA.

Lilie L Lin (LL)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Elizabeth Chiao (E)

Department of Medicine, Baylor College of Medicine, 1155 Pressler St. Unit, Houston, 1340, USA. eychiao@mdanderson.org.
Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, USA. eychiao@mdanderson.org.

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