Evidence map›Paper›PMID 33710337›Full record

ArticleBlood advances2021

Autologous stem cell transplantation after anti-PD-1 therapy for multiply relapsed or refractory Hodgkin lymphoma.

Reid W Merryman, Robert A Redd, Taiga Nishihori, Julio Chavez, Yago Nieto, Justin M Darrah, Uttam Rao, Michael T Byrne, David A Bond, Kami J Maddocks and 32 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

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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

42 authors at 20 institutions in 1 country.

Reid W MerrymanDivision of Hematologic Malignancies and.
Robert A ReddDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA.
Taiga NishihoriDepartment of Blood & Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL.
Julio ChavezDepartment of Blood & Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL.
Yago NietoDepartment of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX.
Justin M DarrahDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA.
Uttam RaoDivision of Hematology-Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Michael T ByrneDivision of Hematology-Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
David A BondDivision of Hematology, Department of Internal Medicine, Arthur G. James Comprehensive Cancer Center, The Ohio State University Hospital, Columbus, OH.
Kami J MaddocksDivision of Hematology, Department of Internal Medicine, Arthur G. James Comprehensive Cancer Center, The Ohio State University Hospital, Columbus, OH.
Michael A SpinnerDivision of Oncology, Department of Medicine, Stanford University, Stanford, CA.
Ranjana H AdvaniDivision of Oncology, Department of Medicine, Stanford University, Stanford, CA.
Hatcher J BallardDivision of Hematology-Oncology, Department of Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA.
Jakub SvobodaDivision of Hematology-Oncology, Department of Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA.
Anurag K SinghDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS.
Joseph P McGuirkDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS.
Dipenkumar ModiDepartment of Oncology, Karmanos Cancer Institute/Wayne State University, Detroit, MI.
Radhakrishnan RamchandrenDivision of Hematology/Oncology, University of Tennessee School of Medicine, Knoxville, TN.
Jason RomancikDepartment of Hematology and Medical Oncology, Emory University-Winship Cancer Institute, Atlanta, GA.
Jonathon B CohenDepartment of Hematology and Medical Oncology, Emory University-Winship Cancer Institute, Atlanta, GA.
Matthew J FrigaultBone Marrow Transplantation Program, Massachusetts General Hospital, Boston, MA.
Yi-Bin ChenBone Marrow Transplantation Program, Massachusetts General Hospital, Boston, MA.
Anthony V SerritellaSection of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL.
Justine KlineSection of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL.
Stephen AnsellDivision of Hematology, Mayo Clinic, Rochester, MN.
Sunita NathanSection of Bone Marrow Transplant and Cell Therapy, Rush University Medical Center, Chicago, IL.
Maryam RahimianBeth Israel Deaconess Medical Center, Boston, MA.
Robin M JoyceBeth Israel Deaconess Medical Center, Boston, MA.
Mansi ShahRutgers Cancer Institute of New Jersey, New Brunswick, NJ.
Kevin A DavidRutgers Cancer Institute of New Jersey, New Brunswick, NJ.
Steven ParkDepartment of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Charlotte, NC.
Anne W BeavenDivision of Hematology, University of North Carolina, Chapel Hill, NC.
Alma HabibDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN.
Veronika BachanovaDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN.
Shazia NakhodaDivision of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA; and.
Nadia KhanDivision of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA; and.
Ryan C LynchUniversity of Washington/Fred Hutchinson Cancer Research Center, Seattle, WA.
Stephen D SmithUniversity of Washington/Fred Hutchinson Cancer Research Center, Seattle, WA.
Vincent T HoDivision of Hematologic Malignancies and.
Ann LaCasceDivision of Hematologic Malignancies and.
Philippe ArmandDivision of Hematologic Malignancies and.
Alex F HerreraDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA.
Beth Israel Deaconess Medical Center · USEmory University · USFox Chase Cancer Center · USHospital of the University of Pennsylvania · USMassachusetts General Hospital · USMoffitt Cancer Center · USRutgers, The State University of New Jersey · USStanford University · USThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USUniversity of Chicago · USUniversity of Kansas Medical Center · USUniversity of Minnesota · USUniversity of Washington · USVanderbilt University Medical Center · USCedars-Sinai Medical Center · USCity of Hope · USDana-Farber Cancer Institute · USLevine Cancer Institute · USMayo Clinic in Arizona · USRush University Medical Center · US

Funding

Transplant for Lymphoma:Therapy-Related LeukemiaP50CA107399 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI KWAK, LARRY W · 2004 to 2022
$35.5M
NCI NIH HHS P50 CA107399
6 · The paper itself

Abstract

Autologous stem cell transplantation (ASCT) can be curative for patients with relapsed/refractory Hodgkin lymphoma (HL). Based on studies suggesting that anti-PD-1 monoclonal antibodies (mAbs) can sensitize patients to subsequent chemotherapy, we hypothesized that anti-PD-1 therapy before ASCT would result in acceptable outcomes among high-risk patients who progressed on or responded insufficiently to ≥1 salvage regimen, including chemorefractory patients who are traditionally considered poor ASCT candidates. We retrospectively identified 78 HL patients who underwent ASCT after receiving an anti-PD-1 mAb (alone or in combination) as third-line or later therapy across 22 centers. Chemorefractory disease was common, including 42 patients (54%) refractory to ≥2 consecutive systemic therapies immediately before anti-PD-1 treatment. Fifty-eight (74%) patients underwent ASCT after anti-PD-1 treatment, while 20 patients (26%) received additional therapy after PD-1 blockade and before ASCT. Patients received a median of 4 systemic therapies (range, 3-7) before ASCT, and 31 patients (41%) had a positive pre-ASCT positron emission tomography (PET) result. After a median post-ASCT follow-up of 19.6 months, the 18-month progression-free survival (PFS) and overall survival were 81% (95% CI, 69-89) and 96% (95% confidence interval [CI], 87-99), respectively. Favorable outcomes were observed for patients who were refractory to 2 consecutive therapies immediately before PD-1 blockade (18-month PFS, 78%), had a positive pre-ASCT PET (18-month PFS, 75%), or received ≥4 systemic therapies before ASCT (18-month PFS, 73%), while PD-1 nonresponders had inferior outcomes (18-month PFS, 51%). In this high-risk cohort, ASCT after anti-PD-1 therapy was associated with excellent outcomes, even among heavily pretreated, previously chemorefractory patients.

Indexed as

Hematopoietic Stem Cell TransplantationHodgkin DiseaseAntineoplastic Combined Chemotherapy ProtocolsHumansNeoplasm Recurrence, LocalRetrospective StudiesTransplantation, Autologous

Identifiers

PMID33710337
PMCPMC7993097
OpenAlexW3133701998

What OpenQuestion holds

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Registered trials

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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.