Cargando…
Eligibility for Human Leukocyte Antigen–Based Therapeutics by Race and Ethnicity
IMPORTANCE: The development of therapeutics for patients who are positive for specific human leukocyte antigen (HLA) subtypes evokes the question of whether certain racial and ethnic groups are more or less likely to be eligible for novel products. OBJECTIVE: To determine whether racial and ethnic i...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Medical Association
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603498/ https://www.ncbi.nlm.nih.gov/pubmed/37883087 http://dx.doi.org/10.1001/jamanetworkopen.2023.38612 |
_version_ | 1785126618161741824 |
---|---|
author | Olivier, Timothée Haslam, Alyson Tuia, Jordan Prasad, Vinay |
author_facet | Olivier, Timothée Haslam, Alyson Tuia, Jordan Prasad, Vinay |
author_sort | Olivier, Timothée |
collection | PubMed |
description | IMPORTANCE: The development of therapeutics for patients who are positive for specific human leukocyte antigen (HLA) subtypes evokes the question of whether certain racial and ethnic groups are more or less likely to be eligible for novel products. OBJECTIVE: To determine whether racial and ethnic inequities were present with regard to trial eligibility in trials investigating a therapeutic restricted to patients with specific HLA subtypes. DESIGN, SETTING, AND PARTICIPANTS: This cross-sectional study included all clinical trials registered in ClinicalTrials.gov through March 18, 2022, that investigated an interventional study of a therapeutic strategy and restricted participants to those with at least 1 HLA subtype. Data were analyzed from May 8 to July 1, 2022. MAIN OUTCOMES AND MEASURES: The type of therapeutics used in trials, the condition under study, the HLA subtypes used, and the likelihood of being enrolled in such a trial according to race and ethnicity. RESULTS: Of 2135 trials identified, 263 met inclusion criteria. Overall, the estimated likelihood of being eligible for an HLA-based trial was 50.3%. Individuals of African American descent had the lowest likelihood of eligibility (33.0%), while being an individual of European descent conferred the highest (53.0%; 1.6 times more likely than African American individuals). Most trials studied anticancer therapeutics (258 [98.1%; 95% CI, 96.4%-99.7%]), and most were a therapeutic vaccine (179 [68.1%; 95% CI, 62.4%-73.7%]). The HLA-A*02:01 allele and the HLA-A2 serotype were the most frequent HLA subtypes for trial eligibility. The frequency of the HLA-A*02:01 allele in the population varied, with 11.9% (95% CI, 11.8%-12.0%) in African or African American individuals and 27.1% (95% CI, 27.1%-27.1%) in individuals of European descent. CONCLUSIONS AND RELEVANCE: The findings of this cross-sectional study suggest that enrollment restrictions for clinical trials investigating novel HLA therapeutics may be associated with racial and ethnic inequities with regard to trial eligibility. Overcoming these restrictions poses biological challenges, but solutions must be implemented to provide equal access to innovative strategies regardless of race or ethnicity. |
format | Online Article Text |
id | pubmed-10603498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Medical Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-106034982023-10-28 Eligibility for Human Leukocyte Antigen–Based Therapeutics by Race and Ethnicity Olivier, Timothée Haslam, Alyson Tuia, Jordan Prasad, Vinay JAMA Netw Open Original Investigation IMPORTANCE: The development of therapeutics for patients who are positive for specific human leukocyte antigen (HLA) subtypes evokes the question of whether certain racial and ethnic groups are more or less likely to be eligible for novel products. OBJECTIVE: To determine whether racial and ethnic inequities were present with regard to trial eligibility in trials investigating a therapeutic restricted to patients with specific HLA subtypes. DESIGN, SETTING, AND PARTICIPANTS: This cross-sectional study included all clinical trials registered in ClinicalTrials.gov through March 18, 2022, that investigated an interventional study of a therapeutic strategy and restricted participants to those with at least 1 HLA subtype. Data were analyzed from May 8 to July 1, 2022. MAIN OUTCOMES AND MEASURES: The type of therapeutics used in trials, the condition under study, the HLA subtypes used, and the likelihood of being enrolled in such a trial according to race and ethnicity. RESULTS: Of 2135 trials identified, 263 met inclusion criteria. Overall, the estimated likelihood of being eligible for an HLA-based trial was 50.3%. Individuals of African American descent had the lowest likelihood of eligibility (33.0%), while being an individual of European descent conferred the highest (53.0%; 1.6 times more likely than African American individuals). Most trials studied anticancer therapeutics (258 [98.1%; 95% CI, 96.4%-99.7%]), and most were a therapeutic vaccine (179 [68.1%; 95% CI, 62.4%-73.7%]). The HLA-A*02:01 allele and the HLA-A2 serotype were the most frequent HLA subtypes for trial eligibility. The frequency of the HLA-A*02:01 allele in the population varied, with 11.9% (95% CI, 11.8%-12.0%) in African or African American individuals and 27.1% (95% CI, 27.1%-27.1%) in individuals of European descent. CONCLUSIONS AND RELEVANCE: The findings of this cross-sectional study suggest that enrollment restrictions for clinical trials investigating novel HLA therapeutics may be associated with racial and ethnic inequities with regard to trial eligibility. Overcoming these restrictions poses biological challenges, but solutions must be implemented to provide equal access to innovative strategies regardless of race or ethnicity. American Medical Association 2023-10-26 /pmc/articles/PMC10603498/ /pubmed/37883087 http://dx.doi.org/10.1001/jamanetworkopen.2023.38612 Text en Copyright 2023 Olivier T et al. JAMA Network Open. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License. |
spellingShingle | Original Investigation Olivier, Timothée Haslam, Alyson Tuia, Jordan Prasad, Vinay Eligibility for Human Leukocyte Antigen–Based Therapeutics by Race and Ethnicity |
title | Eligibility for Human Leukocyte Antigen–Based Therapeutics by Race and Ethnicity |
title_full | Eligibility for Human Leukocyte Antigen–Based Therapeutics by Race and Ethnicity |
title_fullStr | Eligibility for Human Leukocyte Antigen–Based Therapeutics by Race and Ethnicity |
title_full_unstemmed | Eligibility for Human Leukocyte Antigen–Based Therapeutics by Race and Ethnicity |
title_short | Eligibility for Human Leukocyte Antigen–Based Therapeutics by Race and Ethnicity |
title_sort | eligibility for human leukocyte antigen–based therapeutics by race and ethnicity |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603498/ https://www.ncbi.nlm.nih.gov/pubmed/37883087 http://dx.doi.org/10.1001/jamanetworkopen.2023.38612 |
work_keys_str_mv | AT oliviertimothee eligibilityforhumanleukocyteantigenbasedtherapeuticsbyraceandethnicity AT haslamalyson eligibilityforhumanleukocyteantigenbasedtherapeuticsbyraceandethnicity AT tuiajordan eligibilityforhumanleukocyteantigenbasedtherapeuticsbyraceandethnicity AT prasadvinay eligibilityforhumanleukocyteantigenbasedtherapeuticsbyraceandethnicity |