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Horn of plenty: Value of the international registry for pediatric chronic myeloid leukemia
Chronic myeloid leukemia (CML) in minors is a rare disease which can be effectively treated by tyrosine kinase inhibitors (TKIs) since the year 2000. A majority of pediatricians will encounter one or two CML patients in the course of their careers and will typically have to rely on written informati...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450816/ https://www.ncbi.nlm.nih.gov/pubmed/32874947 http://dx.doi.org/10.5306/wjco.v11.i6.308 |
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author | Suttorp, Meinolf Metzler, Markus Millot, Frédéric |
author_facet | Suttorp, Meinolf Metzler, Markus Millot, Frédéric |
author_sort | Suttorp, Meinolf |
collection | PubMed |
description | Chronic myeloid leukemia (CML) in minors is a rare disease which can be effectively treated by tyrosine kinase inhibitors (TKIs) since the year 2000. A majority of pediatricians will encounter one or two CML patients in the course of their careers and will typically have to rely on written information along with their own intuition to provide care. Knowledge of response to TKIs and of age-specific side effects has an impact on the design of pediatric CML trials in many ways aiming to contribute toward greater predictability of clinical improvements. Information from a registry on a rare disease like CML offers the enormous benefit of enabling treating physicians to interact and share their collective experience. The International Registry on Pediatric CML (IR-PCML) was founded at Poitiers/France almost 10 years ago. Since then, the number of collaboration centers and in parallel of registered patients continuously increased (> 550 patients as of December 2019). Ideally, from a given treatment center in a country data are transferred to a national coordinator who interacts with the IR-PCML. In the sense of quality assurance, the registry can offer dissemination of knowledge on state-of-the-art diagnostics (including reference appraisal), optimal treatment approaches, and follow-up procedures within a network that is exerting its strength via participation. With continuous growth during the recent years, very rare subgroups of patients could be identified (e.g., CML diagnosed at age < 3 years, children presenting with specific problems at diagnosis or during course of treatment) which had not been described before. Publications coming from the IR-PCML disseminated this useful information derived from patients who robustly participate and share information about their disease, among themselves and with their caregivers and clinicians. Patient input driving the collection of data on this rare leukemia is the basis for the considerable success of bringing new therapeutics into clinical use. |
format | Online Article Text |
id | pubmed-7450816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-74508162020-08-31 Horn of plenty: Value of the international registry for pediatric chronic myeloid leukemia Suttorp, Meinolf Metzler, Markus Millot, Frédéric World J Clin Oncol Opinion Review Chronic myeloid leukemia (CML) in minors is a rare disease which can be effectively treated by tyrosine kinase inhibitors (TKIs) since the year 2000. A majority of pediatricians will encounter one or two CML patients in the course of their careers and will typically have to rely on written information along with their own intuition to provide care. Knowledge of response to TKIs and of age-specific side effects has an impact on the design of pediatric CML trials in many ways aiming to contribute toward greater predictability of clinical improvements. Information from a registry on a rare disease like CML offers the enormous benefit of enabling treating physicians to interact and share their collective experience. The International Registry on Pediatric CML (IR-PCML) was founded at Poitiers/France almost 10 years ago. Since then, the number of collaboration centers and in parallel of registered patients continuously increased (> 550 patients as of December 2019). Ideally, from a given treatment center in a country data are transferred to a national coordinator who interacts with the IR-PCML. In the sense of quality assurance, the registry can offer dissemination of knowledge on state-of-the-art diagnostics (including reference appraisal), optimal treatment approaches, and follow-up procedures within a network that is exerting its strength via participation. With continuous growth during the recent years, very rare subgroups of patients could be identified (e.g., CML diagnosed at age < 3 years, children presenting with specific problems at diagnosis or during course of treatment) which had not been described before. Publications coming from the IR-PCML disseminated this useful information derived from patients who robustly participate and share information about their disease, among themselves and with their caregivers and clinicians. Patient input driving the collection of data on this rare leukemia is the basis for the considerable success of bringing new therapeutics into clinical use. Baishideng Publishing Group Inc 2020-06-24 2020-06-24 /pmc/articles/PMC7450816/ /pubmed/32874947 http://dx.doi.org/10.5306/wjco.v11.i6.308 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Opinion Review Suttorp, Meinolf Metzler, Markus Millot, Frédéric Horn of plenty: Value of the international registry for pediatric chronic myeloid leukemia |
title | Horn of plenty: Value of the international registry for pediatric chronic myeloid leukemia |
title_full | Horn of plenty: Value of the international registry for pediatric chronic myeloid leukemia |
title_fullStr | Horn of plenty: Value of the international registry for pediatric chronic myeloid leukemia |
title_full_unstemmed | Horn of plenty: Value of the international registry for pediatric chronic myeloid leukemia |
title_short | Horn of plenty: Value of the international registry for pediatric chronic myeloid leukemia |
title_sort | horn of plenty: value of the international registry for pediatric chronic myeloid leukemia |
topic | Opinion Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450816/ https://www.ncbi.nlm.nih.gov/pubmed/32874947 http://dx.doi.org/10.5306/wjco.v11.i6.308 |
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