Evidence map›Paper›PMID 38350338›Full record

ArticleESMO open2024

Treatment-specific risk of subsequent malignant neoplasms in five-year survivors of diffuse large B-cell lymphoma.

Y M Geurts, S I M Neppelenbroek, B M P Aleman, C P M Janus, A D G Krol, D J van Spronsen, W J Plattel, J M Roesink, K M S Verschueren, J M Zijlstra and 20 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in ESMO open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

30 authors at 20 institutions in 4 countries.

Y M GeurtsDepartment of Epidemiology, Netherlands Cancer Institute, Amsterdam.
S I M NeppelenbroekDepartment of Epidemiology, Netherlands Cancer Institute, Amsterdam.
B M P AlemanDepartment of Radiation Oncology, Netherlands Cancer Institute, Amsterdam.
C P M JanusDepartment of Radiotherapy, Erasmus Medical Centre, Rotterdam.
A D G KrolDepartment of Radiation Oncology, Leiden University Medical Centre, Leiden.
D J van SpronsenDepartment of Hematology, Radboud University Medical Centre, Nijmegen.
W J PlattelDepartment of Hematology, University Medical Centre Groningen, Groningen.
J M RoesinkDepartment of Radiotherapy, University Medical Centre Utrecht, Utrecht.
K M S VerschuerenDepartment of Radiation Oncology, Institute Verbeeten, Tilburg.
J M ZijlstraDepartment of Hematology, Amsterdam UMC location Vrije Universiteit, Cancer Centre Amsterdam, Amsterdam.
H R KoeneDepartment of Internal Medicine, St. Antonius Hospital, Nieuwegein.
M R NijzielCatharina Cancer Institute, Department of Hemato-Oncology, Catharina Hospital, Eindhoven.
E C SchimmelRadiotherapiegroep, Arnhem.
E de JonghDepartment of Internal Medicine, Albert Schweitzer Hospital, Dordrecht.
F OngDepartment of Radiotherapy, Medisch Spectrum Twente, Enschede.
L C J Te BoomeDepartment of Hematology, Haaglanden Medical Centre, The Hague.
R S van RijnDepartment of Internal Medicine, Medical Centre Leeuwarden, Leeuwarden.
L H BöhmerDepartment of Hematology, Haga Teaching Hospital, The Hague.
B D P TaDepartment of Radiation Oncology (MAASTRO), GROW School for Oncology, Maastricht University Medical Centre+, Maastricht.
H P J VisserDepartment of Hematology, Noordwest Ziekenhuisgroep Alkmaar, Alkmaar.
E F M PosthumaDepartment of Internal Medicine, Reinier de Graaf Hospital, Delft.
Y M BilginDepartment of Internal Medicine, ADRZ, Goes.
K MullerRadiotherapiegroep, Deventer.
D van KampenZuidwest Radiotherapeutisch Instituut, Vlissingen.
C So-OsmanDepartment of Hematology, Erasmus Medical Centre, Rotterdam; Unit Transfusion Medicine, Sanquin Blood Supply Foundation, Amsterdam.
J S P VermaatDepartment of Hematology, Leiden University Medical Centre, Leiden.
R J de WeijerDepartment of Hematology, University Medical Centre Utrecht, Utrecht.
M J KerstenDepartment of Hematology, Amsterdam UMC location University of Amsterdam, Cancer Centre Amsterdam and LYMMCARE, Amsterdam, The Netherlands.
F E van LeeuwenDepartment of Epidemiology, Netherlands Cancer Institute, Amsterdam.
M SchaapveldDepartment of Epidemiology, Netherlands Cancer Institute, Amsterdam. Electronic address: m.schaapveld@nki.nl.
The Netherlands Cancer Institute · NLAmsterdam University Medical Centers · NLRadboud University Nijmegen · NLRadiotherapiegroep · NLUniversity Medical Center Utrecht · NLAdmiraal De Ruyter Ziekenhuis · NLAlbert Schweitzer Hospital · GAErasmus University Rotterdam · NLHaga Hospital · NLLeiden University · NLLeiden University Medical Center · NLMaastricht University Medical Centre · NLMedisch Centrum Haaglanden · NLMedisch Centrum Leeuwarden · NLMedisch Spectrum Twente · NLNoordwest Ziekenhuisgroep · NLRadiation Oncology Institute · USReinier de Graaf Hospital · NLSanquin · NLSt. Antonius Ziekenhuis · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe introduction of rituximab significantly improved the prognosis of diffuse large B-cell lymphoma (DLBCL), emphasizing the importance of evaluating the long-term consequences of exposure to radiotherapy, alkylating agents and anthracycline-containing (immuno)chemotherapy among DLBCL survivors.

methodsLong-term risk of subsequent malignant neoplasms (SMNs) was examined in a multicenter cohort comprising 2373 5-year DLBCL survivors treated at ages 15-61 years in 1989-2012. Observed SMN numbers were compared with expected cancer incidence to estimate standardized incidence ratios (SIRs) and absolute excess risks (AERs/10 000 person-years). Treatment-specific risks were assessed using multivariable Cox regression.

resultsAfter a median follow-up of 13.8 years, 321 survivors developed one or more SMNs (SIR 1.5, 95% CI 1.3-1.8, AER 51.8). SIRs remained increased for at least 20 years after first-line treatment (SIR ≥20-year follow-up 1.5, 95% CI 1.0-2.2, AER 81.8) and were highest among patients ≤40 years at first DLBCL treatment (SIR 2.7, 95% CI 2.0-3.5). Lung (SIR 2.0, 95% CI 1.5-2.7, AER 13.4) and gastrointestinal cancers (SIR 1.5, 95% CI 1.2-2.0, AER 11.8) accounted for the largest excess risks. Treatment with >4500 mg/m

conclusionFive-year DLBCL survivors have an increased risk of SMNs. Risks were higher for survivors ≤40 years at first treatment and survivors treated with >4500 mg/m

Indexed as

Lymphoma, Large B-Cell, DiffuseNeoplasms, Second PrimaryCyclophosphamideDoxorubicinHumansRituximabSurvivorsCyclophosphamideDoxorubicinRituximabalkylating agentsanthracyclinesdiffuse large B-cell lymphomaradiotherapysubsequent neoplasmssurvivorship

Identifiers

PMID38350338
PMCPMC10937196
OpenAlexW4391756421

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.