Evidence map›Paper›PMID 12176878›Full record

Trial reportBlood2002

High-dose immunosuppressive therapy for severe systemic sclerosis: initial outcomes.

Peter A McSweeney, Richard A Nash, Keith M Sullivan, Jan Storek, Leslie J Crofford, Roger Dansey, Maureen D Mayes, Kevin T McDonagh, J Lee Nelson, Theodore A Gooley and 9 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 2 pooled it
9.7field-weighted citation impact, top 1% 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

56 citing papers in PubMed, 2 syntheses or guidelines pooled it, 185 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Trial
  4. Trial
  5. Manufacture of Autologous CD34Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2017
    Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Stem cell therapy in systemic sclerosis.Clinical rheumatology · 2025
    Review
  13. Observational
  14. Stem cell-based therapy for systemic sclerosis.Rheumatology advances in practice · 2023
    Review
  15. Review
  16. Article
  17. Review
  18. Observational
  19. Systemic Sclerosis as an Indication for Autologous Hematopoietic Cell Transplantation: Position Statement from the American Society for Blood and Marrow Transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2018
    Review
  20. 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

19 authors at 6 institutions in 1 country.

Peter A McSweeneyUniversity of Colorado Health Sciences Center, Denver 80262, USA. peter.mcsweeney@uchsc.edu
Richard A Nash
Keith M Sullivan
Jan Storek
Leslie J Crofford
Roger Dansey
Maureen D Mayes
Kevin T McDonagh
J Lee Nelson
Theodore A Gooley
Leona A Holmberg
C S Chen
Mark H Wener
Katherine Ryan
Julie Sunderhaus
Ken Russell
John Rambharose
Rainer Storb
Daniel E Furst
Wayne State University · USUniversity of Michigan–Ann Arbor · USDuke University · USLoma Linda University · USUniversity of Colorado Health · USThe Barbara Ann Karmanos Cancer Institute · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Thomas James Lynch · 1985 to 2026
$296.4M
ZINC GLUCONATE GLYCINE LOZENGES &VITAMIN C EFFECTS ON COMMON COLDM01RR000042 · NCRR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ORAL, ELIF ARIOGLU · 1985 to 2007
$40.8M
UNRELATED AND HLA-MISMATCHED RELATED DONOR TRANSPLANTSP01HL036444 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI STORB, RAINER F. · 1986 to 2010
$25.9M
STEM CELL TRANSPLANTATION FOR TX OF AUTOIMMUNE DISEASES-N01AI5419N01AI005419 · NIAID · DUKE UNIVERSITY · PI SULLIVAN, KEITH M · 2000 to 2006
$6.2M
T CELL RECONSTITUTION AFTER STEM CELL AUTOGRAFTINGR01AI046108 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI STOREK, JAN · 1999 to 2003
$1.1M
NCI NIH HHS CA15704NCI NIH HHS P30 CA015704NCRR NIH HHS M01 RR000042NCRR NIH HHS M01-RR00042NHLBI NIH HHS HL03701NHLBI NIH HHS HL36444NHLBI NIH HHS P01 HL036444NIAID NIH HHS AI46108NIAID NIH HHS N01 AI005419PHS HHS N01-A1-05410
6 · The paper itself

Abstract

Systemic sclerosis (SSc) is a multisystem disease of presumed autoimmune pathogenesis for which no proven effective treatment exists. High-dose immunosuppressive therapy (HDIT) has been proposed as an investigational treatment for severe autoimmune diseases. Nineteen patients with poor-prognosis SSc underwent HDIT. The median age was 40 years (range, 23-61 years), the median modified Rodnan skin score (a measure of dermal sclerosis) was 31, and the median DLCO was 57%. Conditioning therapy involved 800 cGy total body irradiation (TBI) (+/- lung shielding to approximately 200 cGy), 120 mg/kg cyclophosphamide, and 90 mg/kg equine antithymocyte globulin. CD34-selected granulocyte-colony-stimulating factor-mobilized autologous blood stem cells provided hematopoietic rescue. With median follow-up at 14.7 months, the Kaplan-Meier estimated 2-year survival rate was 79%. Three patients died of treatment complications and one of disease progression. Two of the first 8 patients had fatal regimen-related pulmonary injury, a complication not found among 11 subsequent patients who received lung shielding for TBI. Overall, internal organ functions were stable to slightly worse after HDIT, and 4 patients had progressive or nonresponsive disease. As measured by modified Rodnan skin scores and modified health assessment questionnaire disability index (mHAQ-DI) scores, significant disease responses occurred in 12 of 12 patients evaluated at 1 year after HDIT. In conclusion, though important treatment-related toxicities occurred after HDIT for SSc, modifications of initial approaches appear to reduce treatment risks. Responses in skin and mHAQ-DI scores exceed those reported with other therapies, suggesting that HDIT is a promising new therapy for SSc that should be evaluated in prospective randomized studies.

Indexed as

AdultAntigens, CD34Antilymphocyte SerumCombined Modality TherapyCyclophosphamideFemaleGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHematopoietic Stem Cell TransplantationHumansImmunosuppressive AgentsMaleMiddle AgedPilot ProjectsScleroderma, SystemicSurvival AnalysisAntigens, CD34Antilymphocyte SerumCyclophosphamideGranulocyte Colony-Stimulating FactorImmunosuppressive Agents

Identifiers

PMID12176878
PMCPMC2956742
OpenAlexW1876338319

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.