Evidence map›Paper›PMID 31350306›Full record

Trial reportBlood advances2019

A phase 2 study of brentuximab vedotin in patients with CD30-positive advanced systemic mastocytosis.

Jason Gotlib, John H Baird, Tracy I George, Cheryl Langford, Isabel Reyes, Justin Abuel, Cecelia Perkins, Kurt Schroeder, Prithviraj Bose, Srdan Verstovsek

Open access · goldAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Blood advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Prevalence of antibody drug conjugated-induced nausea and vomiting (ADCINV) in patients with cancer.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Treatment of Indolent and Advanced Systemic Mastocytosis.Mediterranean journal of hematology and infectious diseases · 2022
    Review
  11. Avapritinib for Systemic Mastocytosis.Expert review of hematology · 2021
    Article
  12. Review
  13. Systemic Mastocytosis: Multidisciplinary Approach.Mediterranean journal of hematology and infectious diseases · 2021
    Review
  14. Review
  15. 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

10 authors at 3 institutions in 1 country.

Jason GotlibDivision of Hematology, Stanford Cancer Institute, Stanford, CA.
John H BairdDivision of Hematology, Stanford Cancer Institute, Stanford, CA.ORCID 0000-0001-8291-6546
Tracy I GeorgeDepartment of Pathology, University of New Mexico, Albuquerque, NM; and.ORCID 0000-0001-5478-7847
Cheryl LangfordDivision of Hematology, Stanford Cancer Institute, Stanford, CA.
Isabel ReyesDivision of Hematology, Stanford Cancer Institute, Stanford, CA.
Justin AbuelDivision of Hematology, Stanford Cancer Institute, Stanford, CA.
Cecelia PerkinsDivision of Hematology, Stanford Cancer Institute, Stanford, CA.
Kurt SchroederDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
Prithviraj BoseDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
Srdan VerstovsekDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
Stanford Cancer InstituteThe University of Texas MD Anderson Cancer Center · USUniversity of New Mexico · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

There is an unmet need for effective therapies for advanced systemic mastocytosis (advSM). CD30 is expressed on the surface of neoplastic mast cells (MC) in more than 50% of patients with advSM. Brentuximab vedotin (BV) is a CD30-directed antibody-drug conjugate with preclinical evidence supporting both an antineoplastic effect and an attenuation of immunoglobulin E-associated mediator release. These observations are the basis for this phase 2 trial of BV monotherapy (1.8 mg/kg IV every 3 weeks up to 8 cycles) in patients with CD30-positive advSM. The primary objective was to determine the efficacy of BV according to International Working Group-Myeloproliferative Neoplasms Research and Treatment-European Competence Network on Mastocytosis (IWG-MRT-ECNM) response criteria. Secondary objectives included evaluation of safety, changes in bone marrow (BM) MC burden, serum tryptase level, flow cytometric quantification of MC surface expression of CD30, and self-reported symptom burden. The trial enrolled 10 patients with a diagnosis of CD30

Indexed as

AdultAgedAged, 80 and overAntineoplastic Agents, ImmunologicalBiomarkersBrentuximab VedotinFemaleHumansKi-1 AntigenMaleMastocytosis, SystemicMiddle AgedMolecular Targeted TherapyPatient Reported Outcome MeasuresTreatment OutcomeAntineoplastic Agents, ImmunologicalBiomarkersBrentuximab VedotinKi-1 Antigen

Identifiers

PMID31350306
PMCPMC6693006
OpenAlexW2965316070

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.