Evidence map›Paper›PMID 30816957›Full record

ArticleJAMA oncology2019

Maintenance Therapies for Hodgkin and Non-Hodgkin Lymphomas After Autologous Transplantation: A Consensus Project of ASBMT, CIBMTR, and the Lymphoma Working Party of EBMT.

Abraham S Kanate, Ambuj Kumar, Peter Dreger, Martin Dreyling, Steven Le Gouill, Paolo Corradini, Chris Bredeson, Timothy S Fenske, Sonali M Smith, Anna Sureda and 17 more

Erratum issuedOpen access · greenAbstract readConsensus Statement
In one paragraph

Article in JAMA oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 pooled it
5.7field-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

35 citing papers in PubMed, 2 syntheses or guidelines pooled it, 56 citations in OpenAlex.

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  11. Antibody-drug conjugates come of age in oncology.Nature reviews. Drug discovery · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 20 institutions in 7 countries.

Abraham S KanateSection of Hematology and Oncology, West Virginia University, Morgantown, West Virginia.
Ambuj KumarProgram for Comparative Effectiveness Research, University of South Florida Morsani College of Medicine, Tampa.
Peter DregerUniversity of Heidelberg, Heidelberg, Germany.
Martin DreylingDepartment of Medicine III, University Hospital, LMU Munich, Germany.
Steven Le GouillService d'Hématologie, Centre Hospitalo-Universitaire Nantes, Nantes, France.
Paolo CorradiniDepartment of Oncology and Hematology, Fondazione Istituto Nazionale dei Tumori Milano University of Milano, Milano, Italy.
Chris BredesonThe Ottawa Hospital Bone Marrow Transplant Programme, University of Ottawa, Ottawa, Ontario, Canada.
Timothy S FenskeDivision of Hematology and Oncology, Medical College of Wisconsin, Milwaukee.
Sonali M SmithSection of Hematology/Oncology, The University of Chicago, Chicago, Illinois.
Anna SuredaHematology Department, Institut Català d'Oncologia-Hospitalet, Barcelona, Spain.
Alison MoskowitzDepartment of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York.
Jonathan W FriedbergUniversity of Rochester, Rochester, New York.
David J InwardsDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Alex F HerreraDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, California.
Mohamed A Kharfan-DabajaBlood and Marrow Transplantation Program, Division of Hematology-Oncology, Mayo Clinic, Jacksonville, Florida.
Nishitha ReddyDivision of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Silvia MontotoDepartment of Haemato-Oncology, St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.
Stephen P RobinsonUniversity Hospital Bristol NHS Foundation Trust, London, United Kingdom.
Syed A AbutalibSection of Hematology and Oncology, Cancer Treatment Centers of America, Zion, Illinois.
Christian GisselbrechtHôpital Saint Louis, Paris, France.
Julie VoseDivision of Oncology & Hematology, University of Nebraska Medical Center, Omaha.
Ajay GopalUniversity of Washington, Fred Hutchinson Cancer Research Center, Seattle.
Mazyar ShadmanUniversity of Washington, Fred Hutchinson Cancer Research Center, Seattle.
Miguel-Angel PeralesDepartment of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York.
Paul CarpenterUniversity of Washington, Fred Hutchinson Cancer Research Center, Seattle.
Bipin N SavaniDivision of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Mehdi HamadaniDivision of Hematology and Oncology, Medical College of Wisconsin, Milwaukee.
Fred Hutch Cancer Center · USMedical College of Wisconsin · USMemorial Sloan Kettering Cancer Center · USVanderbilt University Medical Center · USBarts Health NHS Trust · GBCancer Treatment Centers of America · USCentre Hospitalier Universitaire de Nantes · FRCity Of Hope National Medical Center · USHeidelberg University · DEHôpital Saint-Louis · FRInstitut Català d'Oncologia · ESLudwig-Maximilians-Universität München · DEMayo Clinic · USMayo Clinic in Florida · USUniversity Hospitals Bristol NHS Foundation Trust · GBUniversity of Chicago · USUniversity of Milan · ITUniversity of Nebraska Medical Center · USUniversity of Ottawa · CAUniversity of Rochester · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
NCI NIH HHS P30 CA008748NCI NIH HHS U24 CA076518
6 · The paper itself

Abstract

importanceMaintenance therapies are often considered as a therapeutic strategy in patients with lymphoma following autologous hematopoietic cell transplantation (auto-HCT) to mitigate the risk of disease relapse. With an evolving therapeutic landscape, where novel drugs are moving earlier in therapy lines, evidence relevant to contemporary practice is increasingly limited. The American Society for Blood and Marrow Transplantation (ASBMT), Center for International Blood and Marrow Transplant Research (CIBMTR), and European Society for Blood and Marrow Transplantation (EBMT) jointly convened an expert panel with diverse expertise and geographical representation to formulate consensus recommendations regarding the use of maintenance and/or consolidation therapies after auto-HCT in patients with lymphoma. OBSERVATIONS: The RAND-modified Delphi method was used to generate consensus statements where at least 75% vote in favor of a recommendation was considered as consensus. The process included 3 online surveys moderated by an independent methodological expert to ensure anonymity and an in-person meeting. The panel recommended restricting the histologic categories covered in this project to Hodgkin lymphoma (HL), mantle cell lymphoma (MCL), diffuse large B-cell lymphoma (DLBCL), and follicular lymphoma. On completion of the voting process, the panel generated 22 consensus statements regarding post auto-HCT maintenance and/or consolidation therapies. The grade A recommendations included endorsement of: (1) brentuximab vedotin (BV) maintenance and/or consolidation in BV-naïve high-risk HL, (2) rituximab maintenance in MCL undergoing auto-HCT after first-line therapy, (3) rituximab maintenance in rituximab-naïve FL, and (4) No post auto-HCT maintenance was recommended in DLBCL. The panel also developed consensus statements for important real-world clinical scenarios, where randomized data are lacking to guide clinical practice. CONCLUSIONS AND RELEVANCE: In the absence of contemporary evidence-based data, the panel found RAND-modified Delphi methodology effective in providing a rigorous framework for developing consensus recommendations for post auto-HCT maintenance and/or consolidation therapies in lymphoma.

Indexed as

Hematopoietic Stem Cell TransplantationMaintenance ChemotherapyAntineoplastic Agents, ImmunologicalBrentuximab VedotinDelphi TechniqueFemaleHodgkin DiseaseHumansLymphoma, Non-HodgkinMaleRituximabTransplantation, AutologousAntineoplastic Agents, ImmunologicalBrentuximab VedotinRituximab

Identifiers

PMID30816957
PMCPMC6988125
OpenAlexW2915997210

What OpenQuestion holds

Textmetadata
LicenceTDM
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.