Evidence map›Paper›PMID 37722357›Full record

ArticleBlood advances2023

Prognostic model using 18F-FDG PET radiomics predicts progression-free survival in relapsed/refractory Hodgkin lymphoma.

Julia Driessen, Gerben J C Zwezerijnen, Heiko Schöder, Marie José Kersten, Alison J Moskowitz, Craig H Moskowitz, Jakoba J Eertink, Martijn W Heymans, Ronald Boellaard, Josée M Zijlstra

3 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.3field-weighted citation impact, top 6% 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.

NCT00255723 phase2completednot on this map

Risk-Adapted High Dose Chemoradiotherapy and Autologous Stem Cell Transplantation for Patients With Relapsed and Primary Refractory Hodgkin's Lymphoma

TypeinterventionalSponsorMemorial Sloan Kettering Cancer CenterRan2004 to 2012Enrolled98ConditionsLymphomaArmscarboplatin, etoposide, ifosfamide
NCT01508312 phase2completednot on this map

Brentuximab Vedotin (SGN-35) in Transplant Eligible Patients With Relapsed or Refractory Hodgkin Lymphoma

TypeinterventionalSponsorMemorial Sloan Kettering Cancer CenterRan2012 to 2024Enrolled66ConditionsHodgkin's LymphomaArmsbrentuximab vedotin (SGN-35), Brentuximab Vedotin (SGN-35)
NCT02280993 phase1unknown statusnot on this map

Phase I/II Feasibility Study Combining Brentuximab Vedotin With Second Line Salvage Chemotherapy (DHAP) in Hodgkin Lymphoma Patients Refractory to First Line Chemotherapy or in First Relapse Who Are Eligible for High Dose Treatment Followed by Autologous Peripheral Blood Stem Cell Transplantation (ASCT)

TypeinterventionalSponsorMarjolein SpieringRan2014 to 2020Enrolled72ConditionsHodgkin Lymphoma, Refractory, RelapseArmsDHAP, Brentuximab Vedotin, Autologous Peripheral Blood Stem Cell Transplantation
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Prognostic value of baselineQuantitative imaging in medicine and surgery · 2026
    Article
  6. Article
  7. Review
  8. Summary Report of the SNMMI AI Task Force Radiomics Challenge 2024.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2025
    Article
  9. Article
  10. Review
  11. Review
  12. The predictive power ofAnnals of hematology · 2025
    Article
  13. Review
  14. Review
  15. Semiquantitative 2-[Frontiers in medicine · 2024
    Review
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

10 authors at 4 institutions in 2 countries.

Julia DriessenDepartment of Hematology, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0001-9364-2501
Gerben J C ZwezerijnenDivision of Imaging and Biomarkers, Cancer Center Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-9571-9362
Heiko SchöderDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-5170-4185
Marie José KerstenDepartment of Hematology, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-8904-3802
Alison J MoskowitzDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-3408-050X
Craig H MoskowitzDepartment of Medicine, Sylvester Comprehensive Cancer Center, Miami, FL.ORCID 0000-0002-9189-3152
Jakoba J EertinkDivision of Imaging and Biomarkers, Cancer Center Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-6094-0016
Martijn W HeymansDepartment of Epidemiology and Data Science, Amsterdam Public Health Research Institute, Amsterdam, The Netherlands.ORCID 0000-0002-3889-0921
Ronald BoellaardDivision of Imaging and Biomarkers, Cancer Center Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-0313-5686
Josée M ZijlstraDivision of Imaging and Biomarkers, Cancer Center Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0003-1074-5922
Amsterdam University Medical Centers · NLMemorial Sloan Kettering Cancer Center · USGGD Amsterdam · NLUniversity of Miami · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Investigating prognostic factors in patients with relapsed or primary refractory classical Hodgkin lymphoma (R/R cHL) is essential to optimize risk-adapted treatment strategies. We built a prognostic model using baseline quantitative 18F-fluorodeoxyglucose positron emission tomography (PET) radiomics features and clinical characteristics to predict the progression-free survival (PFS) among patients with R/R cHL treated with salvage chemotherapy followed by autologous stem cell transplantation. Metabolic tumor volume and several novel radiomics dissemination features, representing interlesional differences in distance, volume, and standard uptake value, were extracted from the baseline PET. Machine learning using backward selection and logistic regression were applied to develop and train the model on a total of 113 patients from 2 clinical trials. The model was validated on an independent external cohort of 69 patients. In addition, we validated 4 different PET segmentation methods to calculate radiomics features. We identified a subset of patients at high risk for progression with significant inferior 3-year PFS outcomes of 38.1% vs 88.4% for patients in the low-risk group in the training cohort (P < .001) and 38.5% vs 75.0% in the validation cohort (P = .015), respectively. The overall survival was also significantly better in the low-risk group (P = .022 and P < .001). We provide a formula to calculate a risk score for individual patients based on the model. In conclusion, we developed a prognostic model for PFS combining radiomics and clinical features in a large cohort of patients with R/R cHL. This model calculates a PET-based risk profile and can be applied to develop risk-stratified treatment strategies for patients with R/R cHL. These trials were registered at www.clinicaltrials.gov as #NCT02280993, #NCT00255723, and #NCT01508312.

Indexed as

Hematopoietic Stem Cell TransplantationHodgkin DiseaseAntineoplastic Combined Chemotherapy ProtocolsClinical Trials as TopicFluorodeoxyglucose F18HumansPositron-Emission TomographyPrognosisProgression-Free SurvivalTransplantation, AutologousFluorodeoxyglucose F18

Identifiers

PMID37722357
PMCPMC10651466
OpenAlexW4386823030

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.