Evidence map›Paper›PMID 39213424›Full record

ArticleBlood advances2024

Evaluation of prognostic factors in patients with high-risk classical Hodgkin lymphoma undergoing autologous transplantation.

Narendranath Epperla, Ying Huang, Amanda F Cashen, John L Vaughn, Walter Hanel, Talha Badar, Stefan K Barta, Paolo F Caimi, Tarsheen K Sethi, Nishitha Reddy and 15 more

Abstract readMulticenter Study
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
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

25 authors.

Narendranath EpperlaDivision of Hematology, Department of Medicine, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH.ORCID 0000-0002-8216-3457
Ying HuangDivision of Hematology, Department of Medicine, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH.
Amanda F CashenDepartment of Medicine, Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO.
John L VaughnDivision of Hematology, Department of Medicine, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH.
Walter HanelDivision of Hematology, Department of Medicine, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH.
Talha BadarDepartment of Medicine, Medical College of Wisconsin, Milwaukee, WI.ORCID 0000-0003-1548-918X
Stefan K BartaDepartment of Medicine, Fox Chase Cancer Center, Philadelphia, PA.
Paolo F CaimiDepartment of Medicine, Case Western Reserve, Cleveland, OH.
Tarsheen K SethiDepartment of Medicine, Smilow Cancer Hospital, Yale New Haven, New Haven, CT.
Nishitha ReddyDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Reem KarmaliDepartment of Medicine, Robert H. Lurie Cancer Center, Northwestern University, Chicago, IL.ORCID 0000-0003-0984-4376
Celeste BelloDepartment of Medicine, H. Lee Moffitt Cancer Center and Research Institute, Lutz, FL.
Julio C ChavezDepartment of Medicine, H. Lee Moffitt Cancer Center and Research Institute, Lutz, FL.
Shalin K KothariDepartment of Medicine, Smilow Cancer Hospital, Yale New Haven, New Haven, CT.
Francisco J Hernandez-IlizaliturriDepartment of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, NY.
Jakub SvobodaDepartment of Medicine, Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA.
Frederick LansiganDepartment of Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, NH.
Martha J GlennDivision of Hematology and Hematologic Malignancies, Department of Medicine, Huntsman Cancer Institute, The University of Utah, Salt Lake City, UT.
Jonathon B CohenDepartment of Medicine, Winship Cancer Institute, Emory University, Atlanta, GA.ORCID 0000-0002-2723-6481
Caryn SorgeDepartment of Medicine, University of Kentucky, Lexington, KY.
Beth ChristianDivision of Hematology, Department of Medicine, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH.
Alex F HerreraDepartment of Medicine, City of Hope National Medical Center, Duarte, CA.ORCID 0000-0002-9665-7415
Mehdi HamadaniDepartment of Medicine, Medical College of Wisconsin, Milwaukee, WI.ORCID 0000-0001-5372-510X
Luciano J CostaDepartment of Medicine, The University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0001-5362-2469
Ana C XavierDepartment of Pediatrics, The University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0002-3659-3798

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
NCATS NIH HHS UL1 TR001863
6 · The paper itself

Abstract

abstractThere are limited data assessing the risk scores for primary treatment failure (PTF) in patients with classical Hodgkin lymphoma (cHL; PTF-cHL) undergoing autologous hematopoietic cell transplantation (auto-HCT). ECLIPSE (Evaluation of Classical Hodgkin Lymphoma patients wIth Primary treatment failure and analySis of outcomEs) is a multicenter retrospective cohort of patients with PTF-cHL (aged ≥15 years) diagnosed on or after 1 January 2005, at 15 US medical centers. PTF was defined as 1 of the following patterns of failure: (1) progressive disease by imaging during or within 6 weeks of completion of frontline chemotherapy (primary progression [PP]); (2) partial response (PR) or stable disease (SD) by imaging after completion of frontline treatment (PR/SD); (3) progression of disease by imaging (and confirmed by biopsy) within 12 months of frontline therapy completion after prior documentation of complete response (CR; early relapse [ER]). A total of 478 patients were included in the analysis. Among these, 217 (45%) were PP, 86 (18%) were PR/SD, and 175 (37%) were ER. The 6-month and 1-year cumulative incidence of nonrelapse mortality after auto-HCT were 0.9% and 1.1%, respectively. The median progression-free survival (PFS) and overall survival (OS) after auto-HCT were 4.33 and 10.09 years, respectively. Although those not in CR at the time of auto-HCT were associated with inferior PFS and OS, advanced age and diagnosis before 2011 were associated with inferior OS. This study showcases the safety and long-term efficacy of auto-HCT, even in patients with high-risk disease who are traditionally considered chemotherapy refractory, and will serve as a benchmark for the ongoing transplant vs no transplant trials.

Indexed as

Hematopoietic Stem Cell TransplantationHodgkin DiseaseTransplantation, AutologousAdolescentAdultAgedFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesRisk FactorsYoung Adult

Identifiers

PMID39213424
PMCPMC11532746

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.