Evidence map›Paper›PMID 35606338›Full record

ArticleHematological oncology2022

Prognostic value of lesion dissemination in doxorubicin, bleomycin, vinblastine, and dacarbazine-treated, interimPET-negative classical Hodgkin Lymphoma patients: A radio-genomic study.

Rexhep Durmo, Benedetta Donati, Louis Rebaud, Anne Segolene Cottereau, Alessia Ruffini, Maria Elena Nizzoli, Sabino Ciavarella, Maria Carmela Vegliante, Christophe Nioche, Michel Meignan and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Hematological oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Article
  7. PSMA-PET-derived distance features as biomarkers for predicting outcomes in primary prostate cancer post-radical prostatectomy.Cancer imaging : the official publication of the International Cancer Imaging Society · 2025
    Article
  8. Article
  9. Article
  10. Baseline and earlyCancer imaging : the official publication of the International Cancer Imaging Society · 2024
    Article
  11. 2-[Annals of hematology · 2024
    Article
  12. Article
  13. Article
  14. IsJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2024
    Article
  15. Article
  16. Semiquantitative 2-[Frontiers in medicine · 2024
    Review
  17. Article
  18. Article
  19. Review
  20. 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

15 authors at 6 institutions in 2 countries.

Rexhep DurmoNuclear Medicine Unit, Azienda USL-IRCCS, Reggio Emilia, Italy.
Benedetta DonatiTranslational Research Laboratory, Azienda USL-IRCCS, Reggio Emilia, Italy.
Louis RebaudLaboratoire d'Imagerie Translationnelle en Oncologie, Institut Curie, U1288 Inserm, PSL, Orsay, France.
Anne Segolene CottereauDepartment of Nuclear Medicine, Cochin Hospital, AP-HP, Université de Paris, Paris, France.
Alessia RuffiniHematology Unit, Azienda USL-IRCCS, Reggio Emilia, Italy.
Maria Elena NizzoliHematology Unit, Azienda USL-IRCCS, Reggio Emilia, Italy.
Sabino CiavarellaHematology and Cell Therapy Unit, IRCCS-Istituto Tumori 'Giovanni Paolo II', Bari, Italy.
Maria Carmela VeglianteHematology and Cell Therapy Unit, IRCCS-Istituto Tumori 'Giovanni Paolo II', Bari, Italy.ORCID https://orcid.org/0000-0002-3165-1768
Christophe NiocheLaboratoire d'Imagerie Translationnelle en Oncologie, Institut Curie, U1288 Inserm, PSL, Orsay, France.
Michel MeignanLysa Imaging, Henri Mondor University Hospital, AP-HP, University Paris East, Creteil, France.
Francesco MerliHematology Unit, Azienda USL-IRCCS, Reggio Emilia, Italy.
Annibale VersariNuclear Medicine Unit, Azienda USL-IRCCS, Reggio Emilia, Italy.
Alessia CiarrocchiTranslational Research Laboratory, Azienda USL-IRCCS, Reggio Emilia, Italy.ORCID https://orcid.org/0000-0002-5541-2075
Irene BuvatLaboratoire d'Imagerie Translationnelle en Oncologie, Institut Curie, U1288 Inserm, PSL, Orsay, France.
Stefano LuminariHematology Unit, Azienda USL-IRCCS, Reggio Emilia, Italy.
Azienda Sanitaria Unità Locale di Reggio Emilia · ITInserm · FRIstituto Tumori Bari · ITUniversity of Modena and Reggio Emilia · ITUniversité Paris Cité · FRUniversité Paris-Est Créteil · FR

Funding

Associazione Italiana per la Ricerca sul CancroGRADE OnlusItalian Ministry of Health - Ricerca Corrente Annual Program 2023
6 · The paper itself

Abstract

We evaluated the prognostic role of the largest distance between two lesions (Dmax), defined by positron emission tomography (PET) in a retrospective cohort of newly diagnosed classical Hodgkin Lymphoma (cHL) patients. We also explored the molecular bases underlying Dmax through a gene expression analysis of diagnostic biopsies. We included patients diagnosed with cHL from 2007 to 2020, initially treated with ABVD, with available baseline PET for review, and with at least two FDG avid lesions. Patients with available RNA from diagnostic biopsy were eligible for gene expression analysis. Dmax was deduced from the three-dimensional coordinates of the baseline metabolic tumor volume (MTV) and its effect on progression free survival (PFS) was evaluated. Gene expression profiles were correlated with Dmax and analyzed using CIBERSORTx algorithm to perform deconvolution. The study was conducted on 155 eligible cHL patients. Using its median value of 20 cm, Dmax was the only variable independently associated with PFS (HR = 2.70, 95% CI 1.1-6.63, pValue = 0.03) in multivariate analysis of PFS for all patients and for those with early complete metabolic response (iPET-). Among patients with iPET-low Dmax was associated with a 4-year PFS of 90% (95% CI 82.0-98.9) significantly better compared to high Dmax (4-year PFS 72.4%, 95% CI 61.9-84.6). From the analysis of gene expression profiles differences in Dmax were mostly associated with variations in the expression of microenvironmental components. In conclusion our results support tumor dissemination measured through Dmax as novel prognostic factor for cHL patients treated with ABVD.

Indexed as

Hodgkin DiseaseAntineoplastic Combined Chemotherapy ProtocolsBleomycinDacarbazineDoxorubicinFluorodeoxyglucose F18GenomicsHumansPositron-Emission TomographyPrognosisRetrospective StudiesRNAVinblastineBleomycinDacarbazineDoxorubicinFluorodeoxyglucose F18RNAVinblastineDmaxgene expression profilingHodgkin's lymphomaPETtumor disseminationtumor microenvironment

Identifiers

PMID35606338
PMCPMC9796042
OpenAlexW4281397645

What OpenQuestion holds

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LicenceCC BY-NC
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.