Evidence map›Paper›PMID 33488609›Full record

ArticleFrontiers in immunology2020

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

Revathi Raj, Fouzia N Aboobacker, Satya Prakash Yadav, Ramya Uppuluri, Sunil Bhat, Dharma Choudhry, Vikas Dua, Gaurav Kharya, Neha Rastogi, Mansi Sachdev and 5 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 8 institutions in 1 country.

Revathi RajDepartment of Pediatric Hematology and Oncology, Apollo Cancer Institutes, Chennai, India.
Fouzia N AboobackerDepartment of Hematology, Christian Medical College, Vellore, India.
Satya Prakash YadavPediatric Hemato-Oncology & BMT Unit, Medanta The Medicity, Gurgaon, India.
Ramya UppuluriDepartment of Pediatric Hematology and Oncology, Apollo Cancer Institutes, Chennai, India.
Sunil BhatDepartment of Pediatric Hematology and Oncology, Narayana Health City, Bangalore, India.
Dharma ChoudhryDepartment of Pediatric Hematology and Oncology, BLK Super Specialty Hospital, New Delhi, India.
Vikas DuaDepartment of Pediatric Hematology and Oncology, Fortis Memorial Research Institute, Gurugram, India.
Gaurav KharyaDepartment of Pediatric Hematology and Oncology, Indraprastha Apollo Hospital, New Delhi, India.
Neha RastogiPediatric Hemato-Oncology & BMT Unit, Medanta The Medicity, Gurgaon, India.
Mansi SachdevDepartment of Pediatric Hematology and Oncology, Fortis Memorial Research Institute, Gurugram, India.
Vipin KhandelwalDepartment of Pediatric Hematology and Oncology, BLK Super Specialty Hospital, New Delhi, India.
Venkateswaran SwaminathanDepartment of Pediatric Hematology and Oncology, Apollo Cancer Institutes, Chennai, India.
Atish BakaneDepartment of Pediatric Hematology and Oncology, Indraprastha Apollo Hospital, New Delhi, India.
Balasubramaniam RamakrishnanDepartment of Biostatistics, Apollo Hospitals, Chennai, India.
Biju GeorgeDepartment of Hematology, Christian Medical College, Vellore, India.
Cancer Institute (WIA) · INBLK Super Speciality Hospital · INChristian Medical College & Hospital · INFortis Memorial Research Institute · INIndraprastha Apollo Hospitals · INMedanta The Medicity · INApollo Hospitals · INNarayana Health · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Hematopoietic Stem Cell TransplantationAdolescentAge FactorsChildChild, PreschoolFemaleGraft vs Host DiseaseHumansIndiaInfantLiving DonorsMalePrimary Immunodeficiency DiseasesRetrospective StudiesRisk AssessmentRisk Factorsconditioninghaploidenticalhematopoietic stem cell transplantIndiaprimary immune deficiency

Identifiers

PMID33488609
PMCPMC7819851
OpenAlexW3118754991

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.