Evidence map›Paper›PMID 39624016›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2025

Autologous Nonmyeloablative Hematopoietic Stem Cell Transplantation for Diffuse Cutaneous Systemic Sclerosis: Identifying Disease Risk Factors for Toxicity and Long-Term Outcomes in a Prospective, Single-Arm Trial.

George E Georges, Dinesh Khanna, Mark H Wener, Matthew G Mei, Maureen D Mayes, Robert W Simms, Vaishali Sanchorawala, Chitra Hosing, Suzanne Kafaja, Attaphol Pawarode and 7 more

Abstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Stem cell therapy in systemic sclerosis.Clinical rheumatology · 2025
    Review
  3. Article
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

17 authors.

George E GeorgesNorthwestern University Feinberg School of Medicine, Chicago, Fred Hutchinson Cancer Center and University of Washington, Seattle.ORCID 0000-0002-0625-0858
Dinesh KhannaUniversity of Michigan, Ann Arbor.ORCID 0000-0003-1412-4453
Mark H WenerUniversity of Washington, Seattle.
Matthew G MeiCity of Hope National Medical Center, Duarte, California.
Maureen D MayesUniversity of Texas Houston, Houston.ORCID 0000-0001-5070-2535
Robert W Simms(current address: Dartmouth Geisel School of Medicine, Hannover, New Hampshire), Boston Medical Center and Boston University, Boston, Massachusetts.
Vaishali Sanchorawala(current address: Dartmouth Geisel School of Medicine, Hannover, New Hampshire), Boston Medical Center and Boston University, Boston, Massachusetts.
Chitra HosingM. D. Anderson Cancer Center, Houston, Texas.
Suzanne KafajaUniversity of California Los Angeles, Los Angeles.
Attaphol PawarodeUniversity of Michigan, Ann Arbor.
Leona A HolmbergFred Hutchinson Cancer Center and University of Washington, Seattle.
Jason KolfenbachUniversity of Colorado Anschutz, Aurora.ORCID 0000-0002-7043-9161
Daniel E FurstUniversity of California Los Angeles, Los Angeles.ORCID 0000-0001-7857-2373
Keith M SullivanDuke University, Durham, North Carolina.ORCID 0000-0002-1379-9216
Suiyuan HuangUniversity of Michigan, Ann Arbor.
Ted GooleyFred Hutchinson Cancer Center, Seattle, Washington.
Richard A NashColorado Blood Cancer Institute, Denver, Colorado.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTwo randomized trials for patients with diffuse systemic sclerosis (SSc) demonstrated an overall survival (OS) and event-free survival (EFS) advantage of autologous hematopoietic stem cell transplantation (AHSCT) using CD34+ selected peripheral blood stem cells (PBSCs) compared with monthly cyclophosphamide (CY). We asked if an unmodified PBSC graft followed by maintenance mycophenolate mofetil (MMF) after AHSCT, instead of a CD34+ selected graft, could provide comparable AHSCT outcomes.

methodsTwenty patients with high-risk SSc were enrolled in a prospective, single-arm trial with CY 200 mg/kg and horse antithymocyte globulin (ATG; CY200/ATG), followed by unmanipulated autologous PBSC, and then MMF maintenance starting at 2 months after AHSCT.

resultsPoint estimates of OS and EFS at 5 years after AHSCT were 85% (95% confidence interval [CI] 60.4%-94.9%) and 75% (95% CI 50%-88.7%), respectively. Median follow-up was 7.5 years (range 5.6-11.6) after transplant for living patients. Eight patients (40%) required intensive care unit treatment early after transplant. Early transplant-related mortality occurred in two patients (10%). Five patients developed relapse/progression of SSc after AHSCT. Four of nine patients with anti-RNA polymerase III antibodies had prior scleroderma renal crisis and the lowest quartile of estimated glomerular filtration rate (eGFR) on study entry; all four patients developed prolonged organ failure/death early after transplant.

conclusionWe observed favorable OS and EFS after AHSCT for patients with SSc, using CY200/ATG, unmanipulated PBSCs, and MMF posttransplant maintenance, which was comparable to trials with CD34+ graft selection. We identified a possible risk factor, pretransplant low eGFR, for adverse outcomes after AHSCT.

Indexed as

Hematopoietic Stem Cell TransplantationImmunosuppressive AgentsScleroderma, DiffuseAdultAgedAntilymphocyte SerumCyclophosphamideFemaleHumansMaleMiddle AgedMycophenolic AcidProspective StudiesRisk FactorsTransplantation, AutologousTreatment OutcomeAntilymphocyte SerumCyclophosphamideImmunosuppressive AgentsMycophenolic Acid

Identifiers

PMID39624016
PMCPMC12039467

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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.