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Treatment Options for Paediatric Anaplastic Large Cell Lymphoma (ALCL): Current Standard and beyond
Anaplastic Lymphoma Kinase (ALK)-positive Anaplastic Large Cell Lymphoma (ALCL), remains one of the most curable cancers in the paediatric setting; multi-agent chemotherapy cures approximately 65–90% of patients. Over the last two decades, major efforts have focused on improving the survival rate by...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923354/ https://www.ncbi.nlm.nih.gov/pubmed/29601554 http://dx.doi.org/10.3390/cancers10040099 |
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author | Prokoph, Nina Larose, Hugo Lim, Megan S. Burke, G. A. Amos Turner, Suzanne D. |
author_facet | Prokoph, Nina Larose, Hugo Lim, Megan S. Burke, G. A. Amos Turner, Suzanne D. |
author_sort | Prokoph, Nina |
collection | PubMed |
description | Anaplastic Lymphoma Kinase (ALK)-positive Anaplastic Large Cell Lymphoma (ALCL), remains one of the most curable cancers in the paediatric setting; multi-agent chemotherapy cures approximately 65–90% of patients. Over the last two decades, major efforts have focused on improving the survival rate by intensification of combination chemotherapy regimens and employing stem cell transplantation for chemotherapy-resistant patients. More recently, several new and ‘renewed’ agents have offered the opportunity for a change in the paradigm for the management of both chemo-sensitive and chemo-resistant forms of ALCL. The development of ALK inhibitors following the identification of the EML4-ALK fusion gene in Non-Small Cell Lung Cancer (NSCLC) has opened new possibilities for ALK-positive ALCL. The uniform expression of CD30 on the cell surface of ALCL has given the opportunity for anti-CD30 antibody therapy. The re-evaluation of vinblastine, which has shown remarkable activity as a single agent even in the face of relapsed disease, has led to the consideration of a revised approach to frontline therapy. The advent of immune therapies such as checkpoint inhibition has provided another option for the treatment of ALCL. In fact, the number of potential new agents now presents a real challenge to the clinical community that must prioritise those thought to offer the most promise for the future. In this review, we will focus on the current status of paediatric ALCL therapy, explore how new and ‘renewed’ agents are re-shaping the therapeutic landscape for ALCL, and identify the strategies being employed in the next generation of clinical trials. |
format | Online Article Text |
id | pubmed-5923354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-59233542018-05-03 Treatment Options for Paediatric Anaplastic Large Cell Lymphoma (ALCL): Current Standard and beyond Prokoph, Nina Larose, Hugo Lim, Megan S. Burke, G. A. Amos Turner, Suzanne D. Cancers (Basel) Review Anaplastic Lymphoma Kinase (ALK)-positive Anaplastic Large Cell Lymphoma (ALCL), remains one of the most curable cancers in the paediatric setting; multi-agent chemotherapy cures approximately 65–90% of patients. Over the last two decades, major efforts have focused on improving the survival rate by intensification of combination chemotherapy regimens and employing stem cell transplantation for chemotherapy-resistant patients. More recently, several new and ‘renewed’ agents have offered the opportunity for a change in the paradigm for the management of both chemo-sensitive and chemo-resistant forms of ALCL. The development of ALK inhibitors following the identification of the EML4-ALK fusion gene in Non-Small Cell Lung Cancer (NSCLC) has opened new possibilities for ALK-positive ALCL. The uniform expression of CD30 on the cell surface of ALCL has given the opportunity for anti-CD30 antibody therapy. The re-evaluation of vinblastine, which has shown remarkable activity as a single agent even in the face of relapsed disease, has led to the consideration of a revised approach to frontline therapy. The advent of immune therapies such as checkpoint inhibition has provided another option for the treatment of ALCL. In fact, the number of potential new agents now presents a real challenge to the clinical community that must prioritise those thought to offer the most promise for the future. In this review, we will focus on the current status of paediatric ALCL therapy, explore how new and ‘renewed’ agents are re-shaping the therapeutic landscape for ALCL, and identify the strategies being employed in the next generation of clinical trials. MDPI 2018-03-30 /pmc/articles/PMC5923354/ /pubmed/29601554 http://dx.doi.org/10.3390/cancers10040099 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Prokoph, Nina Larose, Hugo Lim, Megan S. Burke, G. A. Amos Turner, Suzanne D. Treatment Options for Paediatric Anaplastic Large Cell Lymphoma (ALCL): Current Standard and beyond |
title | Treatment Options for Paediatric Anaplastic Large Cell Lymphoma (ALCL): Current Standard and beyond |
title_full | Treatment Options for Paediatric Anaplastic Large Cell Lymphoma (ALCL): Current Standard and beyond |
title_fullStr | Treatment Options for Paediatric Anaplastic Large Cell Lymphoma (ALCL): Current Standard and beyond |
title_full_unstemmed | Treatment Options for Paediatric Anaplastic Large Cell Lymphoma (ALCL): Current Standard and beyond |
title_short | Treatment Options for Paediatric Anaplastic Large Cell Lymphoma (ALCL): Current Standard and beyond |
title_sort | treatment options for paediatric anaplastic large cell lymphoma (alcl): current standard and beyond |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923354/ https://www.ncbi.nlm.nih.gov/pubmed/29601554 http://dx.doi.org/10.3390/cancers10040099 |
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