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Evaluating the endometabolic and bone health effects of Tyrosine Kinase Inhibitors in Chronic Myeloid Leukaemia: a systematic review protocol

INTRODUCTION: Chronic Myeloid Leukaemia (CML) constitutes 15% of new adult leukaemia cases as well as 2%–3% of leukaemia in children under 15% and 9% of leukaemias in adolescents 15–19 years of age annually. The introduction of Tyrosine Kinase Inhibitors (TKI) therapy has dramatically improved survi...

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Autores principales: Balakumaran, Janatani, Birk, Tanisha, Golemiec, Breanne, Helmeczi, Wryan, Inkaran, Jeyanth, Kao, Yun-ya, Leigh, Jennifer, Saliba, Sarah, Sharma, Rishi, Spatafora, Laura, Wright, Kristin, Yao, William, Hillis, Christopher, Banfield, Laura, Thabane, Lehana, Athale, Uma, Samaan, M Constantine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6738716/
https://www.ncbi.nlm.nih.gov/pubmed/31511287
http://dx.doi.org/10.1136/bmjopen-2019-030092
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author Balakumaran, Janatani
Birk, Tanisha
Golemiec, Breanne
Helmeczi, Wryan
Inkaran, Jeyanth
Kao, Yun-ya
Leigh, Jennifer
Saliba, Sarah
Sharma, Rishi
Spatafora, Laura
Wright, Kristin
Yao, William
Hillis, Christopher
Banfield, Laura
Thabane, Lehana
Athale, Uma
Samaan, M Constantine
author_facet Balakumaran, Janatani
Birk, Tanisha
Golemiec, Breanne
Helmeczi, Wryan
Inkaran, Jeyanth
Kao, Yun-ya
Leigh, Jennifer
Saliba, Sarah
Sharma, Rishi
Spatafora, Laura
Wright, Kristin
Yao, William
Hillis, Christopher
Banfield, Laura
Thabane, Lehana
Athale, Uma
Samaan, M Constantine
author_sort Balakumaran, Janatani
collection PubMed
description INTRODUCTION: Chronic Myeloid Leukaemia (CML) constitutes 15% of new adult leukaemia cases as well as 2%–3% of leukaemia in children under 15% and 9% of leukaemias in adolescents 15–19 years of age annually. The introduction of Tyrosine Kinase Inhibitors (TKI) therapy has dramatically improved survival in these patients, yet the off-target effects of this treatment may have long-term health impacts on CML survivors. The risk of adverse health outcomes is especially important in children, where TKI exposure may occur during critical windows of growth and puberty, and patients require treatment for prolonged periods of time. The aim of this systematic review protocol is to report on the methods used to conduct a systematic review to investigate the endometabolic and bone health effects of TKI therapy in CML. METHODS AND ANALYSIS: Searches will be conducted in the Cochrane Central Register of Controlled Trials, EMBASE and MEDLINE from inception on August 1st, 2019. Searches may be updated while performing the systematic review to ensure new evidence is included if applicable. Grey literature search will include ClinicalTrials.gov and ProQuest Dissertations and Theses A&I. We will perform a meta-analysis if there are at least two studies reporting similar populations, interventions, methods and tracking the same outcome measures. The studies should also have similar age and sex distributions. ETHICS AND DISSEMINATION: As this is a systematic review protocol, it does not include patient data; therefore, Research Ethics Board approval is not indicated. The systematic review will be published in a peer-reviewed journal and presented at international conferences. PROSPERO REGISTRATION NUMBER: CRD42018091175.
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spelling pubmed-67387162019-09-25 Evaluating the endometabolic and bone health effects of Tyrosine Kinase Inhibitors in Chronic Myeloid Leukaemia: a systematic review protocol Balakumaran, Janatani Birk, Tanisha Golemiec, Breanne Helmeczi, Wryan Inkaran, Jeyanth Kao, Yun-ya Leigh, Jennifer Saliba, Sarah Sharma, Rishi Spatafora, Laura Wright, Kristin Yao, William Hillis, Christopher Banfield, Laura Thabane, Lehana Athale, Uma Samaan, M Constantine BMJ Open Oncology INTRODUCTION: Chronic Myeloid Leukaemia (CML) constitutes 15% of new adult leukaemia cases as well as 2%–3% of leukaemia in children under 15% and 9% of leukaemias in adolescents 15–19 years of age annually. The introduction of Tyrosine Kinase Inhibitors (TKI) therapy has dramatically improved survival in these patients, yet the off-target effects of this treatment may have long-term health impacts on CML survivors. The risk of adverse health outcomes is especially important in children, where TKI exposure may occur during critical windows of growth and puberty, and patients require treatment for prolonged periods of time. The aim of this systematic review protocol is to report on the methods used to conduct a systematic review to investigate the endometabolic and bone health effects of TKI therapy in CML. METHODS AND ANALYSIS: Searches will be conducted in the Cochrane Central Register of Controlled Trials, EMBASE and MEDLINE from inception on August 1st, 2019. Searches may be updated while performing the systematic review to ensure new evidence is included if applicable. Grey literature search will include ClinicalTrials.gov and ProQuest Dissertations and Theses A&I. We will perform a meta-analysis if there are at least two studies reporting similar populations, interventions, methods and tracking the same outcome measures. The studies should also have similar age and sex distributions. ETHICS AND DISSEMINATION: As this is a systematic review protocol, it does not include patient data; therefore, Research Ethics Board approval is not indicated. The systematic review will be published in a peer-reviewed journal and presented at international conferences. PROSPERO REGISTRATION NUMBER: CRD42018091175. BMJ Publishing Group 2019-09-11 /pmc/articles/PMC6738716/ /pubmed/31511287 http://dx.doi.org/10.1136/bmjopen-2019-030092 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article 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, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Oncology
Balakumaran, Janatani
Birk, Tanisha
Golemiec, Breanne
Helmeczi, Wryan
Inkaran, Jeyanth
Kao, Yun-ya
Leigh, Jennifer
Saliba, Sarah
Sharma, Rishi
Spatafora, Laura
Wright, Kristin
Yao, William
Hillis, Christopher
Banfield, Laura
Thabane, Lehana
Athale, Uma
Samaan, M Constantine
Evaluating the endometabolic and bone health effects of Tyrosine Kinase Inhibitors in Chronic Myeloid Leukaemia: a systematic review protocol
title Evaluating the endometabolic and bone health effects of Tyrosine Kinase Inhibitors in Chronic Myeloid Leukaemia: a systematic review protocol
title_full Evaluating the endometabolic and bone health effects of Tyrosine Kinase Inhibitors in Chronic Myeloid Leukaemia: a systematic review protocol
title_fullStr Evaluating the endometabolic and bone health effects of Tyrosine Kinase Inhibitors in Chronic Myeloid Leukaemia: a systematic review protocol
title_full_unstemmed Evaluating the endometabolic and bone health effects of Tyrosine Kinase Inhibitors in Chronic Myeloid Leukaemia: a systematic review protocol
title_short Evaluating the endometabolic and bone health effects of Tyrosine Kinase Inhibitors in Chronic Myeloid Leukaemia: a systematic review protocol
title_sort evaluating the endometabolic and bone health effects of tyrosine kinase inhibitors in chronic myeloid leukaemia: a systematic review protocol
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6738716/
https://www.ncbi.nlm.nih.gov/pubmed/31511287
http://dx.doi.org/10.1136/bmjopen-2019-030092
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