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Multicenter Outcome of Hematopoietic Stem Cell Transplantation for Primary Immune Deficiency Disorders in India

BACKGROUND: Hematopoietic stem cell transplantation (HSCT) is the curative option for many primary immune deficiency disorders (PID). In the last 5 years, increased awareness, availability of diagnostics based on flow cytometry, genetic testing, improved supportive care, use of reduced toxicity cond...

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Autores principales: Raj, Revathi, Aboobacker, Fouzia N., Yadav, Satya Prakash, Uppuluri, Ramya, Bhat, Sunil, Choudhry, Dharma, Dua, Vikas, Kharya, Gaurav, Rastogi, Neha, Sachdev, Mansi, Khandelwal, Vipin, Swaminathan, Venkateswaran, Bakane, Atish, Ramakrishnan, Balasubramaniam, George, Biju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819851/
https://www.ncbi.nlm.nih.gov/pubmed/33488609
http://dx.doi.org/10.3389/fimmu.2020.606930
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author Raj, Revathi
Aboobacker, Fouzia N.
Yadav, Satya Prakash
Uppuluri, Ramya
Bhat, Sunil
Choudhry, Dharma
Dua, Vikas
Kharya, Gaurav
Rastogi, Neha
Sachdev, Mansi
Khandelwal, Vipin
Swaminathan, Venkateswaran
Bakane, Atish
Ramakrishnan, Balasubramaniam
George, Biju
author_facet Raj, Revathi
Aboobacker, Fouzia N.
Yadav, Satya Prakash
Uppuluri, Ramya
Bhat, Sunil
Choudhry, Dharma
Dua, Vikas
Kharya, Gaurav
Rastogi, Neha
Sachdev, Mansi
Khandelwal, Vipin
Swaminathan, Venkateswaran
Bakane, Atish
Ramakrishnan, Balasubramaniam
George, Biju
author_sort Raj, Revathi
collection PubMed
description BACKGROUND: Hematopoietic stem cell transplantation (HSCT) is the curative option for many primary immune deficiency disorders (PID). In the last 5 years, increased awareness, availability of diagnostics based on flow cytometry, genetic testing, improved supportive care, use of reduced toxicity conditioning, and success of haploidentical donor HSCT have improved access to HSCT for children with PID in India. We present results on children with PID who underwent HSCT across India and the factors that influenced outcome. PATIENTS AND METHODS: We collected retrospective data on the outcome of HSCT for PID from seven centers. We analyzed the impact of the type of PID, conditioning regimen, time period of HSCT- before or after January 2016, graft versus host disease prophylaxis, cause of mortality and overall survival. RESULTS: A total of 228 children underwent HSCT for PID at a median age of 12 months (range, 1 to 220 months) with a median follow up of 14.4 months. Infants accounted for 51.3% of the cohort and the male female ratio was 3:1. SCID (25%) and HLH (25%) were the more frequent diagnoses. Matched family donor was available in 36.4% and 44.3% children had a haploidentical HSCT. Reduced and myeloablative conditioning regimens were used with 64% children receiving a treosulfan based conditioning regimen. Peripheral blood stem cells were the predominant graft source at 69.3%. The survival in infants (60.2%) was inferior to children aged over 1 year (75.7% p value = 0.01). Children with Wiskott Aldrich syndrome (74.3%) and chronic granulomatous disease (82.6%) had the best outcomes. The survival was superior in children receiving HSCT from a matched sibling (78%) versus an alternate donor HSCT (61% p value = 0.04). In the cohort transplanted after January 2016 survival improved from 26.8% to 77.5% (p value = 0.00). Infection remains the main cause of mortality at in over 50% children. The 5-year overall survival rate was 68%. CONCLUSION: Survival of children with PID undergoing HSCT in India has improved dramatically in last 5 years. Alternate donor HSCT is now feasible and has made a therapeutic option accessible to all children with PID.
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spelling pubmed-78198512021-01-23 Multicenter Outcome of Hematopoietic Stem Cell Transplantation for Primary Immune Deficiency Disorders in India Raj, Revathi Aboobacker, Fouzia N. Yadav, Satya Prakash Uppuluri, Ramya Bhat, Sunil Choudhry, Dharma Dua, Vikas Kharya, Gaurav Rastogi, Neha Sachdev, Mansi Khandelwal, Vipin Swaminathan, Venkateswaran Bakane, Atish Ramakrishnan, Balasubramaniam George, Biju Front Immunol Immunology BACKGROUND: Hematopoietic stem cell transplantation (HSCT) is the curative option for many primary immune deficiency disorders (PID). In the last 5 years, increased awareness, availability of diagnostics based on flow cytometry, genetic testing, improved supportive care, use of reduced toxicity conditioning, and success of haploidentical donor HSCT have improved access to HSCT for children with PID in India. We present results on children with PID who underwent HSCT across India and the factors that influenced outcome. PATIENTS AND METHODS: We collected retrospective data on the outcome of HSCT for PID from seven centers. We analyzed the impact of the type of PID, conditioning regimen, time period of HSCT- before or after January 2016, graft versus host disease prophylaxis, cause of mortality and overall survival. RESULTS: A total of 228 children underwent HSCT for PID at a median age of 12 months (range, 1 to 220 months) with a median follow up of 14.4 months. Infants accounted for 51.3% of the cohort and the male female ratio was 3:1. SCID (25%) and HLH (25%) were the more frequent diagnoses. Matched family donor was available in 36.4% and 44.3% children had a haploidentical HSCT. Reduced and myeloablative conditioning regimens were used with 64% children receiving a treosulfan based conditioning regimen. Peripheral blood stem cells were the predominant graft source at 69.3%. The survival in infants (60.2%) was inferior to children aged over 1 year (75.7% p value = 0.01). Children with Wiskott Aldrich syndrome (74.3%) and chronic granulomatous disease (82.6%) had the best outcomes. The survival was superior in children receiving HSCT from a matched sibling (78%) versus an alternate donor HSCT (61% p value = 0.04). In the cohort transplanted after January 2016 survival improved from 26.8% to 77.5% (p value = 0.00). Infection remains the main cause of mortality at in over 50% children. The 5-year overall survival rate was 68%. CONCLUSION: Survival of children with PID undergoing HSCT in India has improved dramatically in last 5 years. Alternate donor HSCT is now feasible and has made a therapeutic option accessible to all children with PID. Frontiers Media S.A. 2021-01-08 /pmc/articles/PMC7819851/ /pubmed/33488609 http://dx.doi.org/10.3389/fimmu.2020.606930 Text en Copyright © 2021 Raj, Aboobacker, Yadav, Uppuluri, Bhat, Choudhry, Dua, Kharya, Rastogi, Sachdev, Khandelwal, Swaminathan, Bakane, Ramakrishnan and George http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Raj, Revathi
Aboobacker, Fouzia N.
Yadav, Satya Prakash
Uppuluri, Ramya
Bhat, Sunil
Choudhry, Dharma
Dua, Vikas
Kharya, Gaurav
Rastogi, Neha
Sachdev, Mansi
Khandelwal, Vipin
Swaminathan, Venkateswaran
Bakane, Atish
Ramakrishnan, Balasubramaniam
George, Biju
Multicenter Outcome of Hematopoietic Stem Cell Transplantation for Primary Immune Deficiency Disorders in India
title Multicenter Outcome of Hematopoietic Stem Cell Transplantation for Primary Immune Deficiency Disorders in India
title_full Multicenter Outcome of Hematopoietic Stem Cell Transplantation for Primary Immune Deficiency Disorders in India
title_fullStr Multicenter Outcome of Hematopoietic Stem Cell Transplantation for Primary Immune Deficiency Disorders in India
title_full_unstemmed Multicenter Outcome of Hematopoietic Stem Cell Transplantation for Primary Immune Deficiency Disorders in India
title_short Multicenter Outcome of Hematopoietic Stem Cell Transplantation for Primary Immune Deficiency Disorders in India
title_sort multicenter outcome of hematopoietic stem cell transplantation for primary immune deficiency disorders in india
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819851/
https://www.ncbi.nlm.nih.gov/pubmed/33488609
http://dx.doi.org/10.3389/fimmu.2020.606930
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