Evidence map›Paper›PMID 28468799›Full record

ArticleBlood2017

PD-1 blockade for relapsed lymphoma post-allogeneic hematopoietic cell transplant: high response rate but frequent GVHD.

Bradley M Haverkos, Diana Abbott, Mehdi Hamadani, Philippe Armand, Mary E Flowers, Reid Merryman, Manali Kamdar, Abraham Sebastian Kanate, Ayman Saad, Amitkumar Mehta and 16 more

Registry-linked trialOpen access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03605589 (A Pilot Study of Blinatumomab in Combination With a PD1 Inhibitor, Pembrolizumab, in Pediatric and Young Adult Patients With Relapsed/Refractory CD19 Positive B-cell Acute Leukemia or Lymphoma), which is not on this map. Cited by 140 papers.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed
27.4field-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.

NCT03605589 phase1withdrawnnot on this mapstarted 2018, after this paper: background citation

A Pilot Study of Blinatumomab in Combination With a PD1 Inhibitor, Pembrolizumab, in Pediatric and Young Adult Patients With Relapsed/Refractory CD19 Positive B-cell Acute Leukemia or Lymphoma

TypeinterventionalSponsorChildren's Hospital Medical Center, CincinnatiRan2018 to 2022Enrolled0ConditionsLeukemia, B-cell, Lymphoma, B-CellArmsBlinatumomab, Pembrolizumab
3 · Its place in the literature

Who cites it

140 citing papers in PubMed, 239 citations in OpenAlex.

  1. Over-expression of PD-1 Does Not Predict Leukemic Relapse after Allogeneic Stem Cell Transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Trial
  2. Shortened-Duration Tacrolimus after Nonmyeloablative, HLA-Haploidentical Bone Marrow Transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2018
    Trial
  3. Biochemistry and biophysics reports · 2026
    Review
  4. The Immune Checkpoint Inhibitors Journey: From Early Promise to Lasting Impact.Journal of immunotherapy and precision oncology · 2026
    Review
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80 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 16 institutions in 1 country.

Bradley M HaverkosDivision of Hematology, University of Colorado School of Medicine, Denver, CO.ORCID 0000-0002-3872-0615
Diana AbbottDivision of Biostatistics, University of Colorado, Denver, CO.
Mehdi HamadaniDivision of Hematology and Oncology, Medical College of Wisconsin and Center for International Blood and Marrow Transplant Research, Milwaukee, WI.
Philippe ArmandDivision of Hematology, Dana-Farber Cancer Institute, Boston, MA.
Mary E FlowersClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Reid MerrymanDivision of Hematology, Dana-Farber Cancer Institute, Boston, MA.
Manali KamdarDivision of Hematology, University of Colorado School of Medicine, Denver, CO.
Abraham Sebastian KanateOsborn Hematopoietic Malignancy and Transplantation Program, West Virginia University, Morgantown, WV.
Ayman SaadBlood and Marrow Transplant Program, University of Alabama at Birmingham, Birmingham, AL.
Amitkumar MehtaBlood and Marrow Transplant Program, University of Alabama at Birmingham, Birmingham, AL.
Siddhartha GangulyDivision of Hematologic Malignancies and Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS.
Timothy S FenskeDivision of Hematology and Oncology, Medical College of Wisconsin and Center for International Blood and Marrow Transplant Research, Milwaukee, WI.
Parameswaran HariDivision of Hematology and Oncology, Medical College of Wisconsin and Center for International Blood and Marrow Transplant Research, Milwaukee, WI.
Robert LowskyDivision of Blood and Marrow Transplantation, Stanford University, Stanford, CA.
Leslie AndritsosDivision of Hematology, The Ohio State University, Columbus, OH.
Madan JagasiaDivision of Hematology-Oncology, Vanderbilt University Medical Center, Nashville, TN.
Asad BasheyBlood and Marrow Transplant Program, Northside Hospital, Atlanta, GA.
Stacey BrownBlood and Marrow Transplant Program, Northside Hospital, Atlanta, GA.
Veronika BachanovaDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN.
Deborah StephensDivision of Hematology and Hematologic Malignancies, University of Utah, Salt Lake City, UT.
Shin MineishiDivision of Hematology, Penn State Cancer Institute, Hershey, PA.
Ryotaro NakamuraDivision of Hematology, City of Hope, Los Angeles, CA.
Yi-Bin ChenMassachusetts General Hospital, Boston, MA; and.
Bruce R BlazarDivision of Pediatric Blood and Marrow Transplantation, University of Minnesota, Minneapolis, MN.
Jonathan GutmanDivision of Hematology, University of Colorado School of Medicine, Denver, CO.
Steven M DevineDivision of Hematology, The Ohio State University, Columbus, OH.
University of Colorado Denver · USMedical College of Wisconsin · USDana-Farber Cancer Institute · USNorthside Hospital · USThe Ohio State University · USUniversity of Alabama at Birmingham · USUniversity of Minnesota · USCity of Hope · USFred Hutch Cancer Center · USMassachusetts General Hospital · USPennsylvania State University · USStanford Blood Center · USUniversity of Kansas Medical Center · USUniversity of Utah · USVanderbilt University Medical Center · USWest Virginia University · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Mark J Osborn · 1995 to 2026
$48.2M
Transgenic/KnockoutP01AI056299 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SHARPE, ARLENE H. · 2003 to 2023
$42.5M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)KL2TR000113 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$5.4M
In Vivo Prevention of Murine GVHDR37AI034495 · NIAID · UNIVERSITY OF MINNESOTA · PI Bruce R Blazar · 2017 to 2026
$5.4M
NCATS NIH HHS KL2 TR000113NCATS NIH HHS UL1 TR000114NCI NIH HHS L30 CA189070NCI NIH HHS P01 CA065493NCI NIH HHS P30 CA046934NIAID NIH HHS P01 AI056299NIAID NIH HHS R37 AI034495
6 · The paper itself

Abstract

Given the limited treatment options for relapsed lymphoma post-allogeneic hematopoietic cell transplantation (post-allo-HCT) and the success of programmed death 1 (PD-1) blockade in classical Hodgkin lymphoma (cHL) patients, anti-PD-1 monoclonal antibodies (mAbs) are increasingly being used off-label after allo-HCT. To characterize the safety and efficacy of PD-1 blockade in this setting, we conducted a multicenter retrospective analysis of 31 lymphoma patients receiving anti-PD-1 mAbs for relapse post-allo-HCT. Twenty-nine (94%) patients had cHL and 27 had ≥1 salvage therapy post-allo-HCT and prior to anti-PD-1 treatment. Median follow-up was 428 days (range, 133-833) after the first dose of anti-PD-1. Overall response rate was 77% (15 complete responses and 8 partial responses) in 30 evaluable patients. At last follow-up, 11 of 31 patients progressed and 21 of 31 (68%) remain alive, with 8 (26%) deaths related to new-onset graft-versus-host disease (GVHD) after anti-PD-1. Seventeen (55%) patients developed treatment-emergent GVHD after initiation of anti-PD-1 (6 acute, 4 overlap, and 7 chronic), with onset after a median of 1, 2, and 2 doses, respectively. GVHD severity was grade III-IV acute or severe chronic in 9 patients. Only 2 of these 17 patients achieved complete response to GVHD treatment, and 14 of 17 required ≥2 systemic therapies. In conclusion, PD-1 blockade in relapsed cHL allo-HCT patients appears to be highly efficacious but frequently complicated by rapid onset of severe and treatment-refractory GVHD. PD-1 blockade post-allo-HCT should be studied further but cannot be recommended for routine use outside of a clinical trial.

Indexed as

Hematopoietic Stem Cell TransplantationAdultAgedAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsFemaleGene ExpressionGraft vs Host DiseaseHodgkin DiseaseHumansMaleMiddle AgedNeoplasm Recurrence, LocalNivolumabProgrammed Cell Death 1 ReceptorAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsNivolumabPDCD1 protein, humanpembrolizumabProgrammed Cell Death 1 Receptor

Identifiers

PMID28468799
PMCPMC5510790
OpenAlexW2611189127

What OpenQuestion holds

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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.