Evidence map›Paper›PMID 41905703›Full record

GuidelineTransplantation and cellular therapy2026

Gene Therapy for Sickle Cell Disease: Practice Recommendations from the American Society for Transplantation and Cellular Therapy and the International Society for Cell & Gene Therapy.

Akshay Sharma, Adetola Kassim, Alexis Thompson, David A Williams, Hien D Liu, Jaap J Boelens, James L LaBelle, John Tisdale, Josu de la Fuente, Julie Kanter and 10 more

Abstract readReviewPractice Guideline
In one paragraph

Guideline in Transplantation and cellular therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

20 authors.

Akshay SharmaDepartment of Bone Marrow Transplantation & Cellular Therapy, St Jude Children's Research Hospital, Memphis, Tennessee.
Adetola KassimVanderbilt University Medical Center, Nashville, Tennessee.
Alexis ThompsonChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania.
David A WilliamsDivision of Hematology/Oncology, Department of Pediatric Oncology, Boston Children's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Hien D LiuDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, Florida.
Jaap J BoelensMemorial Sloan Kettering Cancer Center, New York, New York.
James L LaBelleThe University of Chicago, Chicago, Illinois.
John TisdaleCellular and Molecular Therapeutics, National Institutes of Health, Bethesda, Maryland.
Josu de la FuenteDepartment of Paediatrics, St. Mary's Hospital, Imperial College Healthcare NHS Trust, London, UK.
Julie KanterLifespan Comprehensive Sickle Cell Center, University of Alabama at Birmingham School of Medicine, Birmingham, Alabama.
Lakshmanan KrishnamurtiPediatric Hematology and Oncology, Smilow Cancer Hospital at Yale, New Haven, Connecticut.
Lydia H PeckerDivision of Hematology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Mark C WaltersBlood & Marrow Transplant Program, Benioff Children's Hospitals, Oakland, California.
Mary EapenDivision of Hematology-Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Matt PorteusDivision of Hematology, Oncology, and Stem Cell Transplant and Regenerative Medicine, Department of Pediatrics, Stanford Medicine, Palo Alto, California.
Monica BhatiaColumbia University/New York-Presbyterian Morgan Stanley Children's Hospital, New York, New York.
Sandeep SoniMammoth Biosciences, Inc., Brisbane, California; Department of Pediatrics, University of California San Francisco, San Francisco, California.
Selim CorbaciogluDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, University of Regensburg, Regensburg, Germany.
Tami D JohnDivision of Hematology, Oncology, and Stem Cell Transplant and Regenerative Medicine, Department of Pediatrics, Stanford Medicine, Palo Alto, California.
María I CancioMemorial Sloan Kettering Cancer Center, New York, New York. Electronic address: canciom@mskcc.org.

Funding

Novel therapeutic gene editing to induce fetal hemoglobin for sickle cell diseaseU01HL163983 · NHLBI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Akshay Sharma, Shengdar Tsai · 2023 to 2026
$4.9M
Clinical and genetic risk factors associated with adverse long-term health outcomes after curative therapies in individuals with sickle cell diseaseU01HL156620 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DEBAUN, MICHAEL R., FITZHUGH, COURTNEY D · 2021 to 2025
$4.1M
OVARIAN RESERVE IN POST-MENARCHAL FEMALES WITH SICKLE CELL ANEMIAK23HL146841 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI PECKER, LYDIA · 2020 to 2024
$1.2M
NHLBI NIH HHS K23 HL146841NHLBI NIH HHS U01 HL156620NHLBI NIH HHS U01 HL163983
6 · The paper itself

Abstract

Gene therapy has emerged as a transformative treatment option for individuals with sickle cell disease (SCD), with recent regulatory approvals marking a pivotal shift in clinical care. However, the complexity of patient selection, stem cell mobilization, manufacturing, conditioning, and long-term follow-up underscores the need for standardized, evidence-informed guidance. This consensus document, derived from early clinical experience and developed by the American Society for Transplantation and Cellular Therapy and the International Society for Cell & Gene Therapy, provides practical recommendations for the clinical implementation of ex vivo gene therapies for SCD. Key areas addressed include eligibility assessment, comparative considerations with allogeneic hematopoietic cell transplantation, mobilization and apheresis strategies, conditioning with myeloablative chemotherapy, fertility preservation, psychosocial care, manufacturing quality attributes, and lifelong surveillance for late effects. Collectively, these recommendations aim to harmonize clinical practice; support shared decision-making; and promote safe, equitable, and durable delivery of gene therapy for individuals with SCD.

Indexed as

Anemia, Sickle CellCell- and Tissue-Based TherapyGenetic TherapyHematopoietic Stem Cell TransplantationGene Therapy AgentsHumansSocieties, MedicalUnited Statesgene therapySickle cell disease

Identifiers

PMID41905703
PMCPMC13041730

What OpenQuestion holds

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Registered trials

None linked

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.