Evidence map›Paper›PMID 24370862›Full record

Trial reportBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2014

Unrelated donor allogeneic hematopoietic stem cell transplantation for patients with hemoglobinopathies using a reduced-intensity conditioning regimen and third-party mesenchymal stromal cells.

Sandhya Kharbanda, Angela R Smith, Stephanie K Hutchinson, David H McKenna, James B Ball, Lawrence S Lamb, Rajni Agarwal, Kenneth I Weinberg, John E Wagner

Registry-linked trialOpen access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00957931 (Pilot Study MUD HCT), which is not on this map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 6% 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.

NCT00957931 phase2completednot on this map

Pilot Study MUD HCT:Pts High Risk Sickle Cell,Other Non-Malignant RBC Disorders- Reduced Intensity Preparative Regimen, HAPLO-Identical Mesenchymal Stromal Cells

TypeinterventionalSponsorStanford UniversityRan2009 to 2013Enrolled6ConditionsSickle Cell Disease, Thalassemia, Diamond-Blackfan AnemiaArmsBone marrow transplantation, Mesenchymal Stromal Cells
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 57 citations in OpenAlex.

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  13. Bone Marrow-Derived Mesenchymal Stromal Cells from Patients with Sickle Cell Disease Display Intact Functionality.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2017
    Article
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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

9 authors at 4 institutions in 1 country.

Sandhya KharbandaDivision of Pediatric Hematology/Oncology/Stem Cell Transplantation, Stanford University, Palo Alto, California. Electronic address: ksandhya@stanford.edu.
Angela R SmithDivision of Blood and Marrow Transplant Program, University of Minnesota, Minneapolis, Minnesota.
Stephanie K HutchinsonDivision of Pediatric Hematology/Oncology/Stem Cell Transplantation, Stanford University, Palo Alto, California.
David H McKennaDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota.
James B BallRocky Mountain Pediatric Hematology Oncology, Rocky Mountain Hospital for Children, Denver, Colorado.
Lawrence S LambDepartments of Medicine and Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.
Rajni AgarwalDivision of Pediatric Hematology/Oncology/Stem Cell Transplantation, Stanford University, Palo Alto, California.
Kenneth I WeinbergDivision of Pediatric Hematology/Oncology/Stem Cell Transplantation, Stanford University, Palo Alto, California.
John E WagnerDivision of Blood and Marrow Transplant Program, University of Minnesota, Minneapolis, Minnesota.
Stanford University · USUniversity of Minnesota · USRocky Mountain Hospital for Children · USUniversity of Alabama at Birmingham · US

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Mark J Osborn · 1995 to 2026
$48.2M
NCI NIH HHS P01 CA065493NCI NIH HHS P30 CA077598NHLBI NIH HHS N01 HB037164NHLBI NIH HHS N01 HB 07200
6 · The paper itself

Abstract

Allogeneic hematopoietic stem cell transplantation for patients with a hemoglobinopathy can be curative but is limited by donor availability. Although positive results are frequently observed in those with an HLA-matched sibling donor, use of unrelated donors has been complicated by poor engraftment, excessive regimen-related toxicity, and graft-versus-host disease (GVHD). As a potential strategy to address these obstacles, a pilot study was designed that incorporated both a reduced-intensity conditioning and mesenchymal stromal cells (MSCs). Six patients were enrolled, including 4 with high-risk sickle cell disease (SCD) and 2 with transfusion-dependent thalassemia major. Conditioning consisted of fludarabine (150 mg/m(2)), melphalan (140 mg/m(2)), and alemtuzumab (60 mg for patients weighing > 30 kg and .9 mg/kg for patients weighing <30 kg). Two patients received HLA 7/8 allele matched bone marrow and 4 received 4-5/6 HLA matched umbilical cord blood as the source of HSCs. MSCs were of bone marrow origin and derived from a parent in 1 patient and from an unrelated third-party donor in the remaining 5 patients. GVHD prophylaxis consisted of cyclosporine A and mycophenolate mofetil. One patient had neutropenic graft failure, 2 had autologous hematopoietic recovery, and 3 had hematopoietic recovery with complete chimerism. The 2 SCD patients with autologous hematopoietic recovery are alive. The remaining 4 died either from opportunistic infection, GVHD, or intracranial hemorrhage. Although no infusion-related toxicity was seen, the cotransplantation of MSCs was not sufficient for reliable engraftment in patients with advanced hemoglobinopathy. Although poor engraftment has been observed in nearly all such trials to date in this patient population, there was no evidence to suggest that MSCs had any positive impact on engraftment. Because of the lack of improved engraftment and unacceptably high transplant-related mortality, the study was prematurely terminated. Further investigations into understanding the mechanisms of graft resistance and development of strategies to overcome this barrier are needed to move this field forward.

Indexed as

Cord Blood Stem Cell TransplantationMesenchymal Stem Cell TransplantationAdolescentAlemtuzumabAnemia, Sickle CellAntibodies, Monoclonal, Humanizedbeta-ThalassemiaChildFemaleGraft vs Host DiseaseHistocompatibility TestingHLA AntigensHumansMaleMelphalanMyeloablative AgonistsAlemtuzumabAntibodies, Monoclonal, HumanizedfludarabineHLA AntigensMelphalanMyeloablative AgonistsVidarabineBone marrowEngraftmentGraft-versus-host diseaseHematopoietic stem cell transplantHemoglobinopathiesMesenchymal stromal cellsReduced-intensity conditioningSickle cell diseaseThalassemiaUmbilical cord

Identifiers

PMID24370862
PMCPMC3998675
OpenAlexW2160181865

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.