Evidence map›Paper›PMID 24488560›Full record

Trial reportHaematologica2014

A phase II multicenter rabbit anti-thymocyte globulin trial in patients with myelodysplastic syndromes identifying a novel model for response prediction.

Rami S Komrokji, Adam W Mailloux, Dung-Tsa Chen, Mikkael A Sekeres, Ronald Paquette, William J Fulp, Chiharu Sugimori, Jennifer Paleveda-Pena, Jaroslaw P Maciejewski, Alan F List and 1 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Haematologica, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00466843 (Mechanism and Response of Thymoglobulin in Patients With Myelodysplastic Syndrome), which is not on this map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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.

NCT00466843 phase2unknown statusnot on this map

Mechanism and Response of Thymoglobulin in Patients With Myelodysplastic Syndrome (MDS)

TypeinterventionalSponsorOffice of Rare Diseases (ORD)Ran2007 to 2010Enrolled54ConditionsMyelodysplastic SyndromeArmsAntithymocyte globulin (ATG), Prednisone
3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Review
  7. Vaccines: a promising therapy for myelodysplastic syndrome.Journal of hematology & oncology · 2024
    Review
  8. Review
  9. Haematologica · 2023
    Article
  10. Myelodysplastic syndromes.Nature reviews. Disease primers · 2022
    Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Therapy for lower-risk MDS.Hematology. American Society of Hematology. Education Program · 2020
    Article
  16. Lowering the boom on lower-risk myelodysplastic syndromes.Hematology. American Society of Hematology. Education Program · 2019
    Review
  17. Review
  18. Infections in Myelodysplastic Syndrome in Relation to Stage and Therapy.Mediterranean journal of hematology and infectious diseases · 2018
    Review
  19. Treatment of low-risk myelodysplastic syndromes.Hematology. American Society of Hematology. Education Program · 2016
    Review
  20. Immune Mechanisms in Myelodysplastic Syndrome.International journal of molecular sciences · 2016
    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

11 authors at 4 institutions in 2 countries.

Rami S KomrokjiMalignant Hematology Division, H. Lee Moffitt Cancer Center, Tampa, FL, USA.
Adam W MaillouxImmunology Program, H. Lee Moffitt Cancer Center, Tampa, FL, USA.
Dung-Tsa ChenBiostatistics Program, H. Lee H. Lee Moffitt Cancer Center, Tampa, FL, USA.
Mikkael A SekeresCleveland Clinic Taussig Cancer Institute, Cleveland, OH, USA.
Ronald PaquetteUCLA Medical Center, Los Angeles, CA, USA.
William J FulpBiostatistics Program, H. Lee H. Lee Moffitt Cancer Center, Tampa, FL, USA.
Chiharu SugimoriIshikawa Prefectural Central Hospital, Kuratsukihigashi, Kanazawa, Japan.
Jennifer Paleveda-PenaMalignant Hematology Division, H. Lee Moffitt Cancer Center, Tampa, FL, USA.
Jaroslaw P MaciejewskiCleveland Clinic Taussig Cancer Institute, Cleveland, OH, USA.
Alan F ListMalignant Hematology Division, H. Lee Moffitt Cancer Center, Tampa, FL, USA.
Pearlie K Epling-BurnetteImmunology Program, H. Lee Moffitt Cancer Center, Tampa, FL, USA Pearlie.Burnette@moffitt.org.
Moffitt Cancer Center · USCleveland Clinic · USIshikawa Prefectural Central Hospital · JPUCLA Medical Center · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
CSRD VA I01 CX000114NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

Immune dysregulation is a mechanism contributing to ineffective hematopoiesis in a subset of myelodysplastic syndrome patients. We report the first US multicenter non-randomized, phase II trial examining the efficacy of rabbit(r)-anti-thymocyte globulin using 2.5 mg/kg/day administered daily for 4 doses. The primary end point was hematologic response; secondary end points included duration of response, time to response, time to progression, and tolerance. Nine (33%;95% confidence interval=17%-54%) of the 27 patients treated experienced durable hematologic improvement in an intent-to-treat analysis with a median time to response and median response duration of 75 and 245 days, respectively. While younger age is the most significant factor favoring equine(e)-anti-thymocyte globulin response, treatment outcome on this study was independent of age (P=0.499). A shorter duration between diagnosis and treatment showed a positive trend (P=0.18), but International Prognostic Scoring System score (P=0.150), karyotype (P=0.319), and age-adjusted bone marrow cellularity (P=0.369) were not associated with response classification. Since activated T-lymphocytes are the primary cellular target of anti-thymocyte globulin, a T-cell expression profiling was conducted in a cohort of 38 patients consisting of rabbit and equine-antithymocyte globulin-treated patients. A model containing disease duration, CD8 terminal memory T cells and T-cell proliferation-associated-antigen expression predicted response with the greatest accuracy using a leave-one-out cross validation approach. This profile categorized patients independent of other covariates, including treatment type and age using a leave-one-out-cross-validation approach (75.7%). Therefore, rabbit-anti-thymocyte globulin has hematologic remitting activity in myelodysplastic syndrome and a T-cell activation profile has potential utility classifying those who are more likely to respond (NCT00466843 clinicaltrials.gov).

Indexed as

AdultAgedAnimalsAntilymphocyte SerumFemaleFollow-Up StudiesHumansImmunologic FactorsMaleMiddle AgedMyelodysplastic SyndromesPrognosisRabbitsRisk FactorsTime FactorsTreatment OutcomeAntilymphocyte SerumImmunologic Factors

Identifiers

PMID24488560
PMCPMC4077078
OpenAlexW2124135166

What OpenQuestion holds

Textmetadata
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.