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Peripheral T cell receptor diversity is associated with clinical outcomes following ipilimumab treatment in metastatic melanoma
BACKGROUND: Ipilimumab improves overall survival in a subset of patients with metastatic melanoma. Peripheral blood T cell receptor (TCR) repertoire diversity has been associated with favorable outcomes in patients with cancer, but its relevance as a biomarker for ipilimumab outcomes remains unknown...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469400/ https://www.ncbi.nlm.nih.gov/pubmed/26085931 http://dx.doi.org/10.1186/s40425-015-0070-4 |
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author | Postow, Michael A. Manuel, Manuarii Wong, Phillip Yuan, Jianda Dong, Zhiwan Liu, Cailian Perez, Solène Tanneau, Isabelle Noel, Marlène Courtier, Anaïs Pasqual, Nicolas Wolchok, Jedd D. |
author_facet | Postow, Michael A. Manuel, Manuarii Wong, Phillip Yuan, Jianda Dong, Zhiwan Liu, Cailian Perez, Solène Tanneau, Isabelle Noel, Marlène Courtier, Anaïs Pasqual, Nicolas Wolchok, Jedd D. |
author_sort | Postow, Michael A. |
collection | PubMed |
description | BACKGROUND: Ipilimumab improves overall survival in a subset of patients with metastatic melanoma. Peripheral blood T cell receptor (TCR) repertoire diversity has been associated with favorable outcomes in patients with cancer, but its relevance as a biomarker for ipilimumab outcomes remains unknown. FINDINGS: In this pilot study, we analyzed the pre-treatment peripheral blood TCR repertoire in 12 patients with metastatic melanoma who received ipilimumab at 3 mg/kg (clinical benefit, n = 4; no clinical benefit, n = 8). TCR diversity was evaluated using a polymerase chain reaction assay which measures TCR combinatorial diversity between V and J genes from genomic DNA. TCR repertoire diversity was studied through richness (observed V-J rearrangements) and evenness (similarity between the frequencies of specific V-J rearrangements). The Wilcoxon rank sum test was used to compare patients with clinical benefit and those without. Association with benefit in a dichotomized analysis was assessed through a Fisher’s exact test. Overall survival was studied through log-rank analysis. There was a significant difference in richness (p = 0.033) and evenness (p = 0.028) between patients with and without clinical benefit. Dichotomized analysis showed that none of the patients with low richness (n = 0/5, p = 0.081) nor low evenness (n = 0/7, p = 0.01) achieved clinical benefit. There were no significant differences in overall survival. CONCLUSIONS: In this small group of patients, baseline TCR diversity in the peripheral blood was associated with clinical outcomes. Further investigation is ongoing in larger cohorts of patients to explore these preliminary findings and determine whether TCR diversity can be used as a predictive biomarker in cancer immunotherapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40425-015-0070-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4469400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44694002015-06-18 Peripheral T cell receptor diversity is associated with clinical outcomes following ipilimumab treatment in metastatic melanoma Postow, Michael A. Manuel, Manuarii Wong, Phillip Yuan, Jianda Dong, Zhiwan Liu, Cailian Perez, Solène Tanneau, Isabelle Noel, Marlène Courtier, Anaïs Pasqual, Nicolas Wolchok, Jedd D. J Immunother Cancer Short Report BACKGROUND: Ipilimumab improves overall survival in a subset of patients with metastatic melanoma. Peripheral blood T cell receptor (TCR) repertoire diversity has been associated with favorable outcomes in patients with cancer, but its relevance as a biomarker for ipilimumab outcomes remains unknown. FINDINGS: In this pilot study, we analyzed the pre-treatment peripheral blood TCR repertoire in 12 patients with metastatic melanoma who received ipilimumab at 3 mg/kg (clinical benefit, n = 4; no clinical benefit, n = 8). TCR diversity was evaluated using a polymerase chain reaction assay which measures TCR combinatorial diversity between V and J genes from genomic DNA. TCR repertoire diversity was studied through richness (observed V-J rearrangements) and evenness (similarity between the frequencies of specific V-J rearrangements). The Wilcoxon rank sum test was used to compare patients with clinical benefit and those without. Association with benefit in a dichotomized analysis was assessed through a Fisher’s exact test. Overall survival was studied through log-rank analysis. There was a significant difference in richness (p = 0.033) and evenness (p = 0.028) between patients with and without clinical benefit. Dichotomized analysis showed that none of the patients with low richness (n = 0/5, p = 0.081) nor low evenness (n = 0/7, p = 0.01) achieved clinical benefit. There were no significant differences in overall survival. CONCLUSIONS: In this small group of patients, baseline TCR diversity in the peripheral blood was associated with clinical outcomes. Further investigation is ongoing in larger cohorts of patients to explore these preliminary findings and determine whether TCR diversity can be used as a predictive biomarker in cancer immunotherapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40425-015-0070-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-06-16 /pmc/articles/PMC4469400/ /pubmed/26085931 http://dx.doi.org/10.1186/s40425-015-0070-4 Text en © Postow et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Postow, Michael A. Manuel, Manuarii Wong, Phillip Yuan, Jianda Dong, Zhiwan Liu, Cailian Perez, Solène Tanneau, Isabelle Noel, Marlène Courtier, Anaïs Pasqual, Nicolas Wolchok, Jedd D. Peripheral T cell receptor diversity is associated with clinical outcomes following ipilimumab treatment in metastatic melanoma |
title | Peripheral T cell receptor diversity is associated with clinical outcomes following ipilimumab treatment in metastatic melanoma |
title_full | Peripheral T cell receptor diversity is associated with clinical outcomes following ipilimumab treatment in metastatic melanoma |
title_fullStr | Peripheral T cell receptor diversity is associated with clinical outcomes following ipilimumab treatment in metastatic melanoma |
title_full_unstemmed | Peripheral T cell receptor diversity is associated with clinical outcomes following ipilimumab treatment in metastatic melanoma |
title_short | Peripheral T cell receptor diversity is associated with clinical outcomes following ipilimumab treatment in metastatic melanoma |
title_sort | peripheral t cell receptor diversity is associated with clinical outcomes following ipilimumab treatment in metastatic melanoma |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469400/ https://www.ncbi.nlm.nih.gov/pubmed/26085931 http://dx.doi.org/10.1186/s40425-015-0070-4 |
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