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Predictive factors and outcomes for ibrutinib in relapsed/refractory marginal zone lymphoma: a multicenter cohort study
Ibrutinib is effective in the treatment of relapsed/refractory (R/R) marginal zone lymphoma (MZL) with an overall response rate (ORR) of 48%. However, factors associated with response (or lack thereof) to ibrutinib in R/R MZL in clinical practice are largely unknown. To answer this question, we perf...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287914/ https://www.ncbi.nlm.nih.gov/pubmed/35842643 http://dx.doi.org/10.1186/s13045-022-01316-1 |
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author | Epperla, Narendranath Zhao, Qiuhong Chowdhury, Sayan Mullick Shea, Lauren Moyo, Tamara K. Reddy, Nishitha Sheets, Julia Weiner, David M. Geethakumari, Praveen Ramakrishnan Kandarpa, Malathi Bruno, Ximena Jordan Thomas, Colin Churnetski, Michael C. Hsu, Andrew Zurbriggen, Luke Tan, Cherie Lindsey, Kathryn Maakaron, Joseph Caimi, Paolo F. Torka, Pallawi Bello, Celeste Ayyappan, Sabarish Karmali, Reem Kim, Seo-Hyun Kress, Anna Kothari, Shalin Sawalha, Yazeed Christian, Beth David, Kevin A. Greenwell, Irl Brian Janakiram, Murali Kenkre, Vaishalee P. Olszewski, Adam J. Cohen, Jonathon B. Palmisiano, Neil Umyarova, Elvira Wilcox, Ryan A. Awan, Farrukh T. Alderuccio, Juan Pablo Barta, Stefan K. Grover, Natalie S. Ghosh, Nilanjan Bartlett, Nancy L. Herrera, Alex F. Shouse, Geoffrey |
author_facet | Epperla, Narendranath Zhao, Qiuhong Chowdhury, Sayan Mullick Shea, Lauren Moyo, Tamara K. Reddy, Nishitha Sheets, Julia Weiner, David M. Geethakumari, Praveen Ramakrishnan Kandarpa, Malathi Bruno, Ximena Jordan Thomas, Colin Churnetski, Michael C. Hsu, Andrew Zurbriggen, Luke Tan, Cherie Lindsey, Kathryn Maakaron, Joseph Caimi, Paolo F. Torka, Pallawi Bello, Celeste Ayyappan, Sabarish Karmali, Reem Kim, Seo-Hyun Kress, Anna Kothari, Shalin Sawalha, Yazeed Christian, Beth David, Kevin A. Greenwell, Irl Brian Janakiram, Murali Kenkre, Vaishalee P. Olszewski, Adam J. Cohen, Jonathon B. Palmisiano, Neil Umyarova, Elvira Wilcox, Ryan A. Awan, Farrukh T. Alderuccio, Juan Pablo Barta, Stefan K. Grover, Natalie S. Ghosh, Nilanjan Bartlett, Nancy L. Herrera, Alex F. Shouse, Geoffrey |
author_sort | Epperla, Narendranath |
collection | PubMed |
description | Ibrutinib is effective in the treatment of relapsed/refractory (R/R) marginal zone lymphoma (MZL) with an overall response rate (ORR) of 48%. However, factors associated with response (or lack thereof) to ibrutinib in R/R MZL in clinical practice are largely unknown. To answer this question, we performed a multicenter (25 US centers) cohort study and divided the study population into three groups: “ibrutinib responders”—patients who achieved complete or partial response (CR/PR) to ibrutinib; “stable disease (SD)”; and “primary progressors (PP)”—patients with progression of disease as their best response to ibrutinib. One hundred and nineteen patients met the eligibility criteria with 58%/17% ORR/CR, 29% with SD, and 13% with PP. The median PFS and OS were 29 and 71.4 months, respectively, with no difference in PFS or OS based on the ibrutinib line of therapy or type of therapy before ibrutinib. Patients with complex cytogenetics had an inferior PFS (HR = 3.08, 95% CI 1.23–7.67, p = 0.02), while those with both complex cytogenetics (HR = 3.00, 95% CI 1.03–8.68, p = 0.04) and PP (HR = 13.94, 95% CI 5.17–37.62, p < 0.001) had inferior OS. Only primary refractory disease to first-line therapy predicted a higher probability of PP to ibrutinib (RR = 3.77, 95% CI 1.15–12.33, p = 0.03). In this largest study to date evaluating outcomes of R/R MZL treated with ibrutinib, we show that patients with primary refractory disease and those with PP on ibrutinib are very high-risk subsets and need to be prioritized for experimental therapies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-022-01316-1. |
format | Online Article Text |
id | pubmed-9287914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92879142022-07-17 Predictive factors and outcomes for ibrutinib in relapsed/refractory marginal zone lymphoma: a multicenter cohort study Epperla, Narendranath Zhao, Qiuhong Chowdhury, Sayan Mullick Shea, Lauren Moyo, Tamara K. Reddy, Nishitha Sheets, Julia Weiner, David M. Geethakumari, Praveen Ramakrishnan Kandarpa, Malathi Bruno, Ximena Jordan Thomas, Colin Churnetski, Michael C. Hsu, Andrew Zurbriggen, Luke Tan, Cherie Lindsey, Kathryn Maakaron, Joseph Caimi, Paolo F. Torka, Pallawi Bello, Celeste Ayyappan, Sabarish Karmali, Reem Kim, Seo-Hyun Kress, Anna Kothari, Shalin Sawalha, Yazeed Christian, Beth David, Kevin A. Greenwell, Irl Brian Janakiram, Murali Kenkre, Vaishalee P. Olszewski, Adam J. Cohen, Jonathon B. Palmisiano, Neil Umyarova, Elvira Wilcox, Ryan A. Awan, Farrukh T. Alderuccio, Juan Pablo Barta, Stefan K. Grover, Natalie S. Ghosh, Nilanjan Bartlett, Nancy L. Herrera, Alex F. Shouse, Geoffrey J Hematol Oncol Correspondence Ibrutinib is effective in the treatment of relapsed/refractory (R/R) marginal zone lymphoma (MZL) with an overall response rate (ORR) of 48%. However, factors associated with response (or lack thereof) to ibrutinib in R/R MZL in clinical practice are largely unknown. To answer this question, we performed a multicenter (25 US centers) cohort study and divided the study population into three groups: “ibrutinib responders”—patients who achieved complete or partial response (CR/PR) to ibrutinib; “stable disease (SD)”; and “primary progressors (PP)”—patients with progression of disease as their best response to ibrutinib. One hundred and nineteen patients met the eligibility criteria with 58%/17% ORR/CR, 29% with SD, and 13% with PP. The median PFS and OS were 29 and 71.4 months, respectively, with no difference in PFS or OS based on the ibrutinib line of therapy or type of therapy before ibrutinib. Patients with complex cytogenetics had an inferior PFS (HR = 3.08, 95% CI 1.23–7.67, p = 0.02), while those with both complex cytogenetics (HR = 3.00, 95% CI 1.03–8.68, p = 0.04) and PP (HR = 13.94, 95% CI 5.17–37.62, p < 0.001) had inferior OS. Only primary refractory disease to first-line therapy predicted a higher probability of PP to ibrutinib (RR = 3.77, 95% CI 1.15–12.33, p = 0.03). In this largest study to date evaluating outcomes of R/R MZL treated with ibrutinib, we show that patients with primary refractory disease and those with PP on ibrutinib are very high-risk subsets and need to be prioritized for experimental therapies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-022-01316-1. BioMed Central 2022-07-16 /pmc/articles/PMC9287914/ /pubmed/35842643 http://dx.doi.org/10.1186/s13045-022-01316-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Correspondence Epperla, Narendranath Zhao, Qiuhong Chowdhury, Sayan Mullick Shea, Lauren Moyo, Tamara K. Reddy, Nishitha Sheets, Julia Weiner, David M. Geethakumari, Praveen Ramakrishnan Kandarpa, Malathi Bruno, Ximena Jordan Thomas, Colin Churnetski, Michael C. Hsu, Andrew Zurbriggen, Luke Tan, Cherie Lindsey, Kathryn Maakaron, Joseph Caimi, Paolo F. Torka, Pallawi Bello, Celeste Ayyappan, Sabarish Karmali, Reem Kim, Seo-Hyun Kress, Anna Kothari, Shalin Sawalha, Yazeed Christian, Beth David, Kevin A. Greenwell, Irl Brian Janakiram, Murali Kenkre, Vaishalee P. Olszewski, Adam J. Cohen, Jonathon B. Palmisiano, Neil Umyarova, Elvira Wilcox, Ryan A. Awan, Farrukh T. Alderuccio, Juan Pablo Barta, Stefan K. Grover, Natalie S. Ghosh, Nilanjan Bartlett, Nancy L. Herrera, Alex F. Shouse, Geoffrey Predictive factors and outcomes for ibrutinib in relapsed/refractory marginal zone lymphoma: a multicenter cohort study |
title | Predictive factors and outcomes for ibrutinib in relapsed/refractory marginal zone lymphoma: a multicenter cohort study |
title_full | Predictive factors and outcomes for ibrutinib in relapsed/refractory marginal zone lymphoma: a multicenter cohort study |
title_fullStr | Predictive factors and outcomes for ibrutinib in relapsed/refractory marginal zone lymphoma: a multicenter cohort study |
title_full_unstemmed | Predictive factors and outcomes for ibrutinib in relapsed/refractory marginal zone lymphoma: a multicenter cohort study |
title_short | Predictive factors and outcomes for ibrutinib in relapsed/refractory marginal zone lymphoma: a multicenter cohort study |
title_sort | predictive factors and outcomes for ibrutinib in relapsed/refractory marginal zone lymphoma: a multicenter cohort study |
topic | Correspondence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287914/ https://www.ncbi.nlm.nih.gov/pubmed/35842643 http://dx.doi.org/10.1186/s13045-022-01316-1 |
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