Evidence map›Paper›PMID 42322517›Full record

ArticleLa Radiologia medica2026

Splenic FDG PET uptake and CT volume as prognostic biomarkers in diffuse large B cell lymphoma.

Jacopo D'Argenzio, Nicolò Rampi, Jacopo Pozzi, Valentina Vespro, Matilde Pavan, Elena Casiraghi, Francesca G Rossi, Angelo Castello, Laura V Forzenigo, Massimo Castellani and 3 more

Abstract read
In one paragraph

Article in La Radiologia medica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Jacopo D'Argenzio *Postgraduate School in Radiodiagnostics, Università Degli Studi Di Milano, Via Festa del Perdono 7, 20122, Milan, Italy.
Nicolò Rampi *Hematology Department, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Via Francesco Sforza 35, 20122, Milan, Italy.
Jacopo PozziPostgraduate School in Radiodiagnostics, Università Degli Studi Di Milano, Via Festa del Perdono 7, 20122, Milan, Italy. jacopo.pozzi@unimi.it.ORCID http://orcid.org/0009-0000-6564-6724
Valentina VesproRadiology Department, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Via Francesco Sforza 35, 20122, Milan, Italy.
Matilde PavanPostgraduate School in Radiodiagnostics, Università Degli Studi Di Milano, Via Festa del Perdono 7, 20122, Milan, Italy.
Elena CasiraghiUniversità Degli Studi Di Milano, Via Festa del Perdono 7, 20122, Milan, Italy.
Francesca G RossiHematology Department, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Via Francesco Sforza 35, 20122, Milan, Italy.
Angelo CastelloNuclear Medicine Department, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Via Francesco Sforza 35, 20122, Milan, Italy.
Laura V ForzenigoRadiology Department, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Via Francesco Sforza 35, 20122, Milan, Italy.
Massimo CastellaniNuclear Medicine Department, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Via Francesco Sforza 35, 20122, Milan, Italy.
Massimo ZilocchiRadiology Department, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Via Francesco Sforza 35, 20122, Milan, Italy.
Francesco PassamontiHematology Department, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Via Francesco Sforza 35, 20122, Milan, Italy.
Gianpaolo CarrafielloRadiology Department, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Via Francesco Sforza 35, 20122, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo evaluate whether baseline splenic ^18F-FDG PET uptake and CT-derived spleen volume predict early progression (≤ 36 months) and progression-free survival (PFS) in diffuse large B cell lymphoma (DLBCL), and whether they interact. MATERIALS AND

methodsRetrospective cohort of adults with newly diagnosed DLBCL undergoing baseline ^18F-FDG PET/CT and CT. Splenic PET positivity was defined visually (uptake exceeding hepatic background); spleen volume was measured semi-automatically. Early progression/relapse was analysed as a 36-month milestone endpoint and PFS as time-to-event. Multivariable logistic and Cox models included IPI, sex, treatment, splenic PET, spleen volume, and a PET × volume interaction. A prespecified PFS sensitivity analysis re-included event-free patients censored before 36 months.

results124 patients were included (68 men; median age 68 years [IQR 57-77]); 45/124 (36.3%) were PET-positive; median spleen volume was 3.13 dL (IQR 1.92-5.79). IPI predicted ≤ 36-month progression (OR 1.52; p = 0.021) and PFS (HR 1.44; p = 0.004). Splenic PET positivity predicted ≤ 36-month progression (OR 2.83; p = 0.048) but not PFS (p = 0.103). The PET × volume interaction was significant (OR 0.70; p = 0.021; HR 0.81; p = 0.033). In PET-negative patients, larger spleen volume predicted higher risk (OR 1.42; p = 0.027; HR 1.22; p = 0.042), whereas volume was neutral in PET-positive cases. In the PFS sensitivity analysis (N = 145), the interaction attenuated (HR 0.83; p = 0.057) and the PET-negative volume effect was borderline (HR 1.21; p = 0.053).

conclusionSplenic PET positivity is a dominant risk marker in DLBCL in this cohort. CT-derived spleen volume may add conditional prognostic information in PET-negative patients, but the incremental value of the PET × volume interaction is modest and requires external validation.

Indexed as

Fluorodeoxyglucose F18Lymphoma, Large B-Cell, DiffusePositron Emission Tomography Computed TomographyRadiopharmaceuticalsSpleenTomography, X-Ray ComputedAgedDisease ProgressionFemaleHumansMaleMiddle AgedOrgan SizePredictive Value of TestsPrognosisProgression-Free SurvivalFluorodeoxyglucose F18RadiopharmaceuticalsComputed tomographyDiffuse large B cell lymphomaPositron emission tomographyPrognostic BiomarkersSpleen

Identifiers

PMID42322517
PMCPMC13526055

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