Evidence map›Paper›PMID 31029646›Full record

Trial reportClinical lymphoma, myeloma & leukemia2019

Phase II Study of the PD-1 Inhibitor Pembrolizumab for the Treatment of Relapsed or Refractory Mature T-cell Lymphoma.

Stefan K Barta, Jasmine Zain, Alexander W MacFarlane, Sonali M Smith, Jia Ruan, Henry C Fung, Carlyn R Tan, Yibin Yang, R Katherine Alpaugh, Essel Dulaimi and 7 more

2 registry-linked trialsOpen access · greenAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Clinical lymphoma, myeloma & leukemia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 79 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 2 pooled it
9.8field-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.

NCT02535247 phase1 / phase2terminatednot on this map

A Phase I/II Study to Determine Feasibility and Safety MK-3475 Alone or in Combination With Copanlisib in Relapsed or Refractory NK and T-cell Non-Hodgkin Lymphoma

TypeinterventionalSponsorFox Chase Cancer CenterRan2016 to 2020Enrolled17ConditionsLymphoma, T-Cell, PeripheralArmsMK-3475, Copanlisib
NCT05313243 phase2recruitingnot on this mapstarted 2023, after this paper: background citation

Phase 2 Study of Pembrolizumab and Brentuximab Vedotin in Subjects With Relapsed/Refractory CD30 Positive T-cell Lymphoma

TypeinterventionalSponsorYale UniversityRan2023 to 2028Enrolled32ConditionsT-Cell LymphomaArmsBrentuximab vedotin, Pembrolizumab
3 · Its place in the literature

Who cites it

79 citing papers in PubMed, 2 syntheses or guidelines pooled it, 117 citations in OpenAlex.

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  3. Journal for immunotherapy of cancer · 2025
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  17. BV and beyond: how to incorporate novel agents into PTCL management.Hematology. American Society of Hematology. Education Program · 2024
    Review
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19 more citing papers are in PubMed but not listed here.

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 at 5 institutions in 1 country.

Stefan K BartaDepartment of Hematology and Oncology, Fox Chase Cancer Center, Philadelphia, PA; Department of Hematology and Oncology, University of Pennsylvania, Philadelphia, PA. Electronic address: stefan.barta@uphs.upenn.edu.
Jasmine ZainDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope Cancer Center, Duarte, CA.
Alexander W MacFarlaneDepartment of Blood Cell Development and Function, Fox Chase Cancer Center, Philadelphia, PA.
Sonali M SmithDepartment of Hematology/Oncology, University of Chicago, Chicago, IL.
Jia RuanDepartment of Hematology and Oncology, Weill Cornell Medicine, New York, NY.
Henry C FungDepartment of Hematology and Oncology, Fox Chase Cancer Center, Philadelphia, PA.
Carlyn R TanDepartment of Hematology and Oncology, Fox Chase Cancer Center, Philadelphia, PA.
Yibin YangDepartment of Blood Cell Development and Function, Fox Chase Cancer Center, Philadelphia, PA.
R Katherine AlpaughProtocol Support Laboratory, Fox Chase Cancer Center, Philadelphia, PA.
Essel DulaimiDepartment of Pathology, Fox Chase Cancer Center, Philadelphia, PA.
Eric A RossDepartment of Biostatistics, Fox Chase Cancer Center, Philadelphia, PA.
Kerry S CampbellDepartment of Blood Cell Development and Function, Fox Chase Cancer Center, Philadelphia, PA.
Nadia KhanDepartment of Hematology and Oncology, Fox Chase Cancer Center, Philadelphia, PA.
Rawat SiddhartaOffice of Clinical Research, Fox Chase Cancer Center, Philadelphia, PA.
Nathan H FowlerDepartment of Lymphoma and Myeloma, MD Anderson Cancer Center, Houston, TX.
Richard I FisherDepartment of Hematology and Oncology, Fox Chase Cancer Center, Philadelphia, PA.
Yasuhiro OkiDepartment of Lymphoma and Myeloma, MD Anderson Cancer Center, Houston, TX.
Fox Chase Cancer Center · USThe University of Texas MD Anderson Cancer Center · USCity of Hope · USCornell University · USUniversity of Chicago · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Dietmar J Kappes · 1985 to 2026
$138.8M
NCI NIH HHS P30 CA006927
6 · The paper itself

Abstract

backgroundProgrammed cell death-1 (PD-1) and programmed death-ligand 1 (PD-L1) are frequently expressed in T-cell lymphomas. This provides a rationale for exploration of immune checkpoint inhibitors in the management of T-cell lymphomas. PATIENTS AND

methodsIn this phase II single-arm multicenter trial, patients with relapsed or refractory systemic T-cell lymphoma were treated with 200 mg pembrolizumab intravenously every 21 days. The primary endpoint was progression-free survival (PFS). The secondary endpoints were response rate, overall survival, response duration, and safety. We assessed PD-L1, p-AKT expression, and peripheral blood immune cells as potential predictive biomarkers.

resultsOf 18 enrolled patients, 13 were evaluable for the primary endpoint. The trial was halted early after a preplanned interim futility analysis. The overall response rate was 33% (95% confidence interval [CI], 9%-55%); 4 patients achieved a complete response (27%; 95% CI, 5%-49%). The median PFS was 3.2 months (95% CI, 1.2-3.7 months), and the median overall survival was 10.6 months (95% CI, 3.2-100 months). The median duration of response was 2.9 months (95% CI, 0-10.1 months). Two of the 4 complete responders remain in remission > 15 months. Rash was the most common adverse event (17%; n = 3). The most common ≥ grade 3 treatment-emergent adverse events were rash and pneumonitis (11%; n = 2 each). Neither PD-L1 nor p-AKT expression were associated with outcomes. However, a higher relative frequency of CD4

conclusionPembrolizumab demonstrated modest single-agent activity in relapsed or refractory T-cell lymphoma.

Indexed as

AdolescentAdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalBiomarkers, TumorDrug Resistance, NeoplasmFemaleHumansKaplan-Meier EstimateLymphoma, T-Cell, PeripheralMaleMiddle AgedProgrammed Cell Death 1 ReceptorProto-Oncogene Proteins c-aktAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalBiomarkers, TumorpembrolizumabProgrammed Cell Death 1 ReceptorProto-Oncogene Proteins c-aktAngioimmunoblastic lymphomaImmune checkpoint blockadeImmunotherapyPD-1 inhibitorPeripheral T cell lymphoma

Identifiers

PMID31029646
PMCPMC7433797
OpenAlexW2928054908

What OpenQuestion holds

Textmetadata
LicenceTDM
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.