Evidence map›Paper›PMID 42322070›Full record

Observational studyEuropean journal of haematology2026

Project Sickle Cure: A Prospective, International Observational Study of Hematopoietic Cell Transplantation for Sickle Cell Disease.

Gregory M T Guilcher, Allistair Abraham, Staci D Arnold, Christine Camacho-Bydume, Jenny Duong, Scott Gillespie, Ann Haight, Monica L Hulbert, Naresh Kumar, Katie Liu and 11 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in European journal of haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Gregory M T GuilcherSection of Pediatric Oncology/Transplant, Alberta Children's Hospital, Cumming School of Medicine, University of Calgary, Calgary, Canada.ORCID https://orcid.org/0000-0001-9380-4347
Allistair AbrahamCenter for Cancer and Immunology Research, CETI, Children's National Hospital, Washington, DC, USA.ORCID https://orcid.org/0000-0003-2019-0887
Staci D ArnoldAflac Cancer and Blood Center, Children's Healthcare of Atlanta and Emory University School of Medicine, Atlanta, Georgia, USA.ORCID https://orcid.org/0000-0001-6053-8521
Christine Camacho-BydumeDepartment of Pediatric Hematology/Oncology, Joseph M. Sanzari Children's Hospital, Hackensack University Medical Center, Hackensack, New Jersey, USA.ORCID https://orcid.org/0009-0006-3461-8775
Jenny DuongUniversity of Calgary, Calgary, Canada.
Scott GillespiePediatrics Biostatics Core, Department of Pediatrics, Emory School of Medicine, Atlanta, Georgia, USA.ORCID https://orcid.org/0000-0003-1295-3602
Ann HaightAflac Cancer and Blood Center, Children's Healthcare of Atlanta and Emory University School of Medicine, Atlanta, Georgia, USA.ORCID https://orcid.org/0000-0001-8158-0091
Monica L HulbertDivision of Hematology/Oncology, Boston Children's Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0001-8933-0046
Naresh KumarAflac Cancer and Blood Center, Children's Healthcare of Atlanta and Emory University School of Medicine, Atlanta, Georgia, USA.
Katie LiuPediatrics Biostatics Core, Department of Pediatrics, Emory School of Medicine, Atlanta, Georgia, USA.ORCID https://orcid.org/0009-0003-6851-8340
Cherry MammenDivision of Nephrology, Department of Pediatrics, BC Children's Hospital, Vancouver, Canada.ORCID https://orcid.org/0000-0002-8389-8746
Aleksandra MineykoSection of Pediatric Neurology, Department of Pediatrics, University of Calgary, Calgary, Canada.ORCID https://orcid.org/0000-0002-6735-6111
Abra MorganAflac Cancer and Blood Center, Children's Healthcare of Atlanta and Emory University School of Medicine, Atlanta, Georgia, USA.
Alexander NgwubeTexas Children's Hospital/Baylor College of Medicine, Houston, Texas, USA.ORCID https://orcid.org/0000-0003-4780-5642
Robert S NickelChildren's National Hospital, Washington, DC, USA.ORCID https://orcid.org/0000-0003-4277-7523
Araby RobertsDepartment of Oncology, University of Calgary, Calgary, Canada.ORCID https://orcid.org/0000-0003-4037-3242
Fiona SchulteDepartment of Oncology, University of Calgary, Calgary, Canada.ORCID https://orcid.org/0000-0002-3076-9676
Stephen SandsDepartment of Psychiatry & Behavioral Sciences, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID https://orcid.org/0000-0003-4550-263X
Akshay SharmaDepartment of Bone Marrow Transplantation & Cellular Therapy, St Jude Children's Research Hospital, Memphis, Tennessee, USA.ORCID https://orcid.org/0000-0003-3281-2081
John T HoranGoslisano Children's Hospital, University of Rochester Medical Center, Rochester, New York, USA.
Elizabeth O StengerAflac Cancer and Blood Center, Children's Healthcare of Atlanta and Emory University School of Medicine, Atlanta, Georgia, USA.ORCID https://orcid.org/0000-0002-1386-6685

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Genetix BiotherapeuticsNCI NIH HHS P30 CA008748Patient-Centered Outcomes Research Institute (PCORI) Assessment of Prevention, Diagnosis, and Treatment Options Program Award BPS-2023C1-31041
6 · The paper itself

Abstract

backgroundSickle cell disease (SCD) is a chronic and life-limiting hemoglobin and systemic vascular disease. While over 1000 people have undergone hematopoietic cell transplantation (HCT) over the last 40 years, long-term disease-specific and health-related quality of life data are lacking. The American Society of Hematology 2021 Guidelines for SCD emphasized the need for more detailed registry data to inform patients and providers with decision-making and practice recommendations. PROCEDURES: In January 2021, the Sickle Cell Transplant Advocacy and Research Alliance (STAR) launched Project Sickle Cure (PSC). This multi-center, prospective study of patients who have undergone HCT for SCD includes baseline demographics and SCD-specific post-HCT outcomes, serial neurocognitive testing, health-related quality of life measures, health equity evaluations, a neuroimaging bank, detailed evaluation of neurologic status pre- and post-transplant, and chronic pain evaluation. A biorepository is in the planning stage of development.

resultsAs of November 2025, 115 participants have enrolled at 18 STAR sites with enrollment ongoing.

conclusionsPSC is a STAR prospective study which will address a major gap in our understanding of outcomes post-HCT specific to SCD. WeDecide, a larger study comparing HCT health-related quality of life outcomes to those who receive non-transplant disease modifying therapy (NT-DMT) is in development, and PSC will provide the HCT comparator data. These data will also be highly relevant as other curative and transformative therapies, such as gene therapy, become more widely used.

Indexed as

Anemia, Sickle CellHematopoietic Stem Cell TransplantationAdultFemaleHumansMaleProspective StudiesQuality of LifeTreatment Outcomehealth‐related quality of lifehematopoietic cell transplantationregistrysickle cell disease

Identifiers

PMID42322070
PMCPMC13542865

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.