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Mantle cell lymphoma: A clinical review of the changing treatment paradigms with the advent of novel therapies, and an insight into Indian data

BACKGROUND: Mantle cell lymphoma (MCL) is a rare type of mature B‐cell lymphoid malignancy with the pathologic hallmark of translocation t(11;14) (q13, q32), which leads to an overexpression of Cyclin D1 (CCND1). The disease is also characterized by the presence of a high number of recurrent genetic...

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Autores principales: Radhakrishnan, Vivek Sulekha, Lokireddy, Padmaja, Parihar, Mayur, Prakash, Prashanth Srirangapattana, Menon, Hari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327661/
https://www.ncbi.nlm.nih.gov/pubmed/34821081
http://dx.doi.org/10.1002/cnr2.1590
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author Radhakrishnan, Vivek Sulekha
Lokireddy, Padmaja
Parihar, Mayur
Prakash, Prashanth Srirangapattana
Menon, Hari
author_facet Radhakrishnan, Vivek Sulekha
Lokireddy, Padmaja
Parihar, Mayur
Prakash, Prashanth Srirangapattana
Menon, Hari
author_sort Radhakrishnan, Vivek Sulekha
collection PubMed
description BACKGROUND: Mantle cell lymphoma (MCL) is a rare type of mature B‐cell lymphoid malignancy with the pathologic hallmark of translocation t(11;14) (q13, q32), which leads to an overexpression of Cyclin D1 (CCND1). The disease is also characterized by the presence of a high number of recurrent genetic alterations, which include aberrations in several cellular pathways. MCL is a heterogeneous disease with a wide range of clinical presentations and a majority presenting with aggressive disease in advanced stages. RECENT FINDINGS: Management of MCL is bereft with challenges due to its resistant and relapsing pattern. Despite improvements in remission durations, the disease is currently incurable with standard therapy and has a median survival of about 3–5 years. The use of small molecules like the bruton tyrosine kinase (BTK) and BCL2 inhibitors, for treating relapsed MCL has been established leading to a diminishing role for conventional chemotherapy. Combinations of small molecule inhibitors with or without chemoimmunotherapy, are showing promising results. Cellular therapy in the form of CAR‐T cell therapy, has been approved recently. CONCLUSIONS: Personalized cancer treatment and chemo‐free regimens are showing promise and results from well‐planned long‐term studies are evolving. In India, there is a paucity of epidemiological, clinical, and research data in this field.
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spelling pubmed-93276612022-07-30 Mantle cell lymphoma: A clinical review of the changing treatment paradigms with the advent of novel therapies, and an insight into Indian data Radhakrishnan, Vivek Sulekha Lokireddy, Padmaja Parihar, Mayur Prakash, Prashanth Srirangapattana Menon, Hari Cancer Rep (Hoboken) Review BACKGROUND: Mantle cell lymphoma (MCL) is a rare type of mature B‐cell lymphoid malignancy with the pathologic hallmark of translocation t(11;14) (q13, q32), which leads to an overexpression of Cyclin D1 (CCND1). The disease is also characterized by the presence of a high number of recurrent genetic alterations, which include aberrations in several cellular pathways. MCL is a heterogeneous disease with a wide range of clinical presentations and a majority presenting with aggressive disease in advanced stages. RECENT FINDINGS: Management of MCL is bereft with challenges due to its resistant and relapsing pattern. Despite improvements in remission durations, the disease is currently incurable with standard therapy and has a median survival of about 3–5 years. The use of small molecules like the bruton tyrosine kinase (BTK) and BCL2 inhibitors, for treating relapsed MCL has been established leading to a diminishing role for conventional chemotherapy. Combinations of small molecule inhibitors with or without chemoimmunotherapy, are showing promising results. Cellular therapy in the form of CAR‐T cell therapy, has been approved recently. CONCLUSIONS: Personalized cancer treatment and chemo‐free regimens are showing promise and results from well‐planned long‐term studies are evolving. In India, there is a paucity of epidemiological, clinical, and research data in this field. John Wiley and Sons Inc. 2021-11-24 /pmc/articles/PMC9327661/ /pubmed/34821081 http://dx.doi.org/10.1002/cnr2.1590 Text en © 2021 The Authors. Cancer Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Radhakrishnan, Vivek Sulekha
Lokireddy, Padmaja
Parihar, Mayur
Prakash, Prashanth Srirangapattana
Menon, Hari
Mantle cell lymphoma: A clinical review of the changing treatment paradigms with the advent of novel therapies, and an insight into Indian data
title Mantle cell lymphoma: A clinical review of the changing treatment paradigms with the advent of novel therapies, and an insight into Indian data
title_full Mantle cell lymphoma: A clinical review of the changing treatment paradigms with the advent of novel therapies, and an insight into Indian data
title_fullStr Mantle cell lymphoma: A clinical review of the changing treatment paradigms with the advent of novel therapies, and an insight into Indian data
title_full_unstemmed Mantle cell lymphoma: A clinical review of the changing treatment paradigms with the advent of novel therapies, and an insight into Indian data
title_short Mantle cell lymphoma: A clinical review of the changing treatment paradigms with the advent of novel therapies, and an insight into Indian data
title_sort mantle cell lymphoma: a clinical review of the changing treatment paradigms with the advent of novel therapies, and an insight into indian data
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327661/
https://www.ncbi.nlm.nih.gov/pubmed/34821081
http://dx.doi.org/10.1002/cnr2.1590
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