Evidence map›Paper›PMID 25795722›Full record

ArticleHaematologica2015

Resimmune, an anti-CD3ε recombinant immunotoxin, induces durable remissions in patients with cutaneous T-cell lymphoma.

Arthur E Frankel, Jung H Woo, Chul Ahn, Francine M Foss, Madeleine Duvic, Paul H Neville, David M Neville

4 registry-linked trialsOpen access · goldAbstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in Haematologica, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 4% 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.

NCT00611208 phase2completednot on this map

A Phase II Study of A-dmDT390-bisFv(UCHT1) Fusion Protein in Patients With Cutaneous T Cell Lymphoma

TypeinterventionalSponsorVirogen Biotechnology Inc.Ran2008 to 2016Enrolled32ConditionsT-cell Lymphomas, T-cell Leukemia, Sezary Syndrome, Mycosis FungoidesArmsA-dmDT390-bisFv(UCHT1)
NCT02943642 phase2withdrawnnot on this mapstarted 2026, after this paper: background citation

Safety and Effectiveness of A-dmDT390-bisFv(UCHT1) Fusion Protein (Resimmune®) in Subjects With Mycosis Fungoides: A Phase II Multi-center Randomized Clinical Trial

TypeinterventionalSponsorVirogen Biotechnology Inc.Ran2026 to 2026Enrolled0ConditionsMycosis FungoidesArmsA-dmDT390-bisFv(UCHT1), Vorinostat
NCT02990416 phase1 / phase2unknown statusnot on this mapstarted 2017, after this paper: background citation

Phase I/II Trial of the A-dmDT390-bisFv(UCHT1) Fusion Protein in Combination With Ionizing Radiation and Pembrolizumab for the Treatment of Stage IV Melanoma

TypeinterventionalSponsorVirogen Biotechnology Inc.Ran2017 to 2018Enrolled63ConditionsStage IV MelanomaArmsA-dmDT390-bisFv(UCHT1), Pembrolizumab, Ionizing Radiation
NCT07529405 phase2not yet recruitingnot on this mapstarted 2026, after this paper: background citation

A Phase II Multi-center Randomized Clinical Trial to Determine the Safety and Effectiveness of A-dmDT390-bisFv(UCHT1) Fusion Protein (VG712) in Subjects With Mycosis Fungoides (CurbMF Trial)

TypeinterventionalSponsorVirogen Biotechnology Inc.Ran2026 to 2032Enrolled386ConditionsMycosis FungoidesArmsVG712, Mogamulizumab
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Targeting the Inside of Cells with Biologicals: Toxin Routes in a Therapeutic Context.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2023
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. CD3e-immunotoxin spares CD62LFrontiers in immunology · 2022
    Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. 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

7 authors at 5 institutions in 1 country.

Arthur E FrankelUniversity of Texas Southwestern Medical Center, Dallas, TX arthur.frankel@utsouthwestern.edu.
Jung H WooBaylor Scott & White Health, Temple, TX.
Chul AhnUniversity of Texas Southwestern Medical Center, Dallas, TX.
Francine M FossYale University School of Medicine, New Haven, CT.
Madeleine DuvicThe University of Texas MD Anderson Cancer Center, Houston, TX.
Paul H NevilleAngimmune, LLC, Bethesda, MD, USA.
David M NevilleAngimmune, LLC, Bethesda, MD, USA.
Angimmune (United States) · USThe University of Texas Southwestern Medical Center · USBaylor Scott & White Health · USThe University of Texas MD Anderson Cancer Center · USYale University · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
6 · The paper itself

Abstract

Resimmune is a second-generation recombinant immunotoxin composed of the catalytic and translocation domains of diphtheria toxin fused to two single chain antibody fragments reactive with the extracellular domain of CD3ε. We gave intravenous infusions of Resimmune 2.5 - 11.25 μg/kg over 15 minutes to 30 patients (25 with cutaneous T-cell lymphoma, 3 with peripheral T-cell lymphoma, 1 with T-cell large granular lymphocytic leukemia and 1 with T-cell prolymphocytic leukemia) in an inter-patient dose escalation trial. The most common adverse events were fever, chills, hypotension, edema, hypoalbuminemia, hypophosphatemia, and transaminasemia. Among the 25 patients with cutaneous T-cell lymphoma, there were nine responses for a response rate of 36% (95% CI, 18%-57%) including four complete remissions (16%, 95% CI, 5%-36%). The durations of the complete remissions were 72+, 72+, 60+ and 38+ months. There were five partial remissions lasting 3, 3, 3+, 6+ and 14 months. Of 17 patients with a modified skin weighted assessment tool score <50, 17 patients with stage IB/IIB, and 11 patients with both a score <50 and stage IB/IIB, nine (53%), eight (47%), and eight (73%) had responses, respectively. Further studies of Resimmune in patients with low tumor burden, stage IB-IIB cutaneous T-cell lymphoma are warranted. This trial is registered at clinicaltrials.gov as #NCT00611208.

Indexed as

AdultAgedAged, 80 and overCD3 ComplexCohort StudiesDiphtheria ToxinDose-Response Relationship, DrugFemaleHumansImmunoglobulin FragmentsImmunotoxinsInfusions, IntravenousLymphoma, T-Cell, CutaneousMaleMiddle AgedRecombinant ProteinsCD3 ComplexCD3E protein, humanDiphtheria ToxinImmunoglobulin FragmentsImmunotoxinsRecombinant Proteins

Identifiers

PMID25795722
PMCPMC4450625
OpenAlexW2265537994

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.