Evidence map›Paper›PMID 40270216›Full record

ArticleHaematologica2025

A simplified frailty score predicts outcome in curatively treated older patients with classical Hodgkin lymphoma.

Kjersti Lia, Rasmus Rask Kragh Jørgensen, Per Wikman, Bente L Wold, Ninja Övergaard, Øystein Fluge, Unn-Merete Fagerli, Hanne Bersvendsen, Idun B Bø, Sameer Bhargava and 2 more

Erratum issuedAbstract readValidation Study
In one paragraph

Article in Haematologica, 2025. 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–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

9 citing papers in PubMed.

  1. Article
  2. Haematologica · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
4 · The record

Corrections and comments

  • Erratum issued
    2026
5 · Who and what money

Authors and funding

12 authors.

Kjersti LiaMedical Department, Bærum Hospital, Vestre Viken Hospital Trust, Gjettum, Norway; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway; Department of Oncology, Oslo University Hospital, Oslo. kjerli@vestreviken.no.
Rasmus Rask Kragh JørgensenCenter for Clinical Data Science, Aalborg University and Aalborg University Hospital, Aalborg, Denmark; Department of Hematology, Clinical Cancer Research Centre, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Medicine, Aalborg University, Alborg.
Per WikmanDepartment of Immunology, Genetics and Pathology, Cancer Immunotherapy, Uppsala University, Uppsala.
Bente L WoldDepartment of Oncology, Oslo University Hospital, Oslo.
Ninja ÖvergaardDepartment of Immunology, Genetics and Pathology, Cancer Immunotherapy, Uppsala University, Uppsala, Sweden; Department of Clinical Pathology, Uppsala University, Uppsala.
Øystein FlugeDepartment of Oncology, Haukeland University Hospital, Bergen.
Unn-Merete FagerliDepartment of Oncology, St. Olavs Hospital, Trondheim, Norway; Institute of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, Trondheim.
Hanne BersvendsenDepartment of Oncology, University Hospital of North Norway, Tromsø.
Idun B BøDepartment of Hematology, Stavanger University Hospital, Stavanger, Norway; Institute of Clinical medicine 2, University of Bergen, Bergen.
Sameer BhargavaCancer Registry of Norway, Norwegian Institute of Public Health, Oslo, Norway; South-Eastern Norway Regional Health Authority, Oslo.
Daniel MolinDepartment of Immunology, Genetics and Pathology, Cancer Immunotherapy, Uppsala University, Uppsala.
Alexander FossåDepartment of Oncology, Oslo University Hospital, Oslo, Norway; KG Jebsen Centre for B-cell Malignancies, University of Oslo, Oslo.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Older patients with classical Hodgkin lymphoma (cHL) have lower tolerance and inferior outcomes after standard chemotherapy regimens. To identify patient-derived indicators of frailty associated with outcome, we retrospectively analyzed patient and disease characteristics, treatment and outcome in a Norwegian population-based cohort of older (≥60 years) patients with cHL diagnosed 2000-2015. We included 279 patients (median age 69 years, range 60-90) treated with curative intent, defined as any typical cHL regimen with ≥50% standard doxorubicin dose in the first cycle. In this Norwegian cohort, treatment-related mortality was 8%, median progression-free survival (PFS) and overall survival (OS) were 7.1 years (95% confidence interval [CI]: 5.0-9.3) and 8.7 years (95% CI: 7.0-10.4), respectively. Multivariable analyses identified patient-derived prognostic factors working independently of stage, histology, and International Prognostic Score. We derived a frailty index ranging from 0-3 with one point each for age ≥70 years, Eastern Cooperative Oncology Group status ≥2, and a Cumulative Illness Rating Scale in Geriatrics score ≥8. Patients were categorized as fit (score 0, 34% of patients), unfit (score 1-2, 60%), and frail (score 3, 7%), with 5-year PFS of 74%, 49%, and 11%, and 5-year OS of 86%, 52%, and 22%, respectively. The proposed frailty score was validated in an external cohort of 792 similarly selected patients from the Swedish Lymphoma Register, where comorbidities were scored based on the Charlson comorbidity index (0-2 vs. 3 or higher). In this comprehensive study, we develop a frailty score for elderly cHL patients to inform clinical decisions and prospective trials evaluating selective therapies for older patients.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsFrailtyGeriatric AssessmentHodgkin DiseaseAgedAged, 80 and overClinical Decision-MakingDoxorubicinFemaleHumansMaleMiddle AgedNeoplasm StagingNorwayPrognosisProgression-Free SurvivalDoxorubicin

Identifiers

PMID40270216
PMCPMC12485341

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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.