Evidence map›Paper›PMID 41862725›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2026

Diagnostic brain-to-liver [

Maria Emilia S Takahashi, Tiago P Dos Santos, Christopher Cralcev, Eliana Miranda, Marcos Paulo D S Silva, Felipe C Souza, José Barreto C Carvalheira, Carmino A de Souza, Celso Dario Ramos

Abstract read
In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

9 authors.

Maria Emilia S TakahashiInstituto de Física Gleb Wataghin, Universidade Estadual de Campinas (UNICAMP), Campinas, SP, Brazil.ORCID 0000-0002-3680-6642
Tiago P Dos SantosFaculdade de Ciências Médicas, Universidade Estadual de Campinas (UNICAMP), Campinas, SP, Brazil.ORCID 0009-0002-9755-5506
Christopher CralcevCentro de Hematologia e Hemoterapia, Universidade Estadual de Campinas (UNICAMP), Campinas, SP, Brazil.ORCID 0009-0005-0266-610X
Eliana MirandaCentro de Hematologia e Hemoterapia, Universidade Estadual de Campinas (UNICAMP), Campinas, SP, Brazil.ORCID 0000-0002-7177-7664
Marcos Paulo D S SilvaInstituto de Física Gleb Wataghin, Universidade Estadual de Campinas (UNICAMP), Campinas, SP, Brazil.ORCID 0009-0002-6956-3701
Felipe C SouzaInstituto de Física Gleb Wataghin, Universidade Estadual de Campinas (UNICAMP), Campinas, SP, Brazil.ORCID 0009-0003-3340-1214
José Barreto C CarvalheiraDepartamento de Radiologia e Oncologia, Universidade Estadual de Campinas (UNICAMP), PO Box 6149, Zeferino Vaz Avenue, S/N, 13080-000, Campinas, Brazil.ORCID 0000-0002-0136-0943
Carmino A de SouzaCentro de Hematologia e Hemoterapia, Universidade Estadual de Campinas (UNICAMP), Campinas, SP, Brazil.ORCID 0000-0001-8656-8374
Celso Dario RamosDepartamento de Radiologia e Oncologia, Universidade Estadual de Campinas (UNICAMP), PO Box 6149, Zeferino Vaz Avenue, S/N, 13080-000, Campinas, Brazil. cdramos@unicamp.br.ORCID 0000-0002-1312-1026

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose[¹⁸F]FDG PET/CT has been widely used in oncology for diagnosis and treatment monitoring. Reduced cerebral [¹⁸F]FDG uptake has been observed in patients with disseminated malignancies, potentially associated with the Warburg effect and elevated lactate levels. This study investigated the prognostic relevance of the brain-to-liver [¹⁸F]FDG uptake ratio (BLR) in MM patients who underwent PET/CT at diagnosis.

methodsBLR was calculated as the ratio between the mean standardized uptake value (SUV) of the whole brain and that of the liver. A total of 72 patients were retrospectively included in the study (58% male; median age 65 years (IQR55;70); 67% were classified as ISS stage III).

resultsBLR, as a continuous variable, showed a statistically significant difference between groups according to sex (p = 0.004), overweight status (p = 0.005), and ISS stage (p = 0.03), and was negatively correlated with β₂-microglobulin (r= - 0.42, p < 0.001). With a median follow-up of 23 months (IQR 8; 65), 74% patients had died from MM-related causes. Patients with BLR > 2.7 demonstrated superior 60-month overall survival (52%vs.10%, p = 0.002) and progression-free survival (19%vs.3%, p = 0.003), respectively. Multivariate Cox regression confirmed BLR (HR 1.86 95%CI: 1.03-3.33, p = 0.038 (OS); HR 1.93 95%CI: 1.13-3.29, p = 0.016 (PFS))as an independent factor and the use of autologous hematopoietic cell transplantation (HCT) as consolidation for both OS and PFS. In addition, ISS stage III was also a prognostic factor for OS.

conclusionHigher brain-to-liver [¹⁸F]FDG uptake ratio (> 2.7) at diagnosis predicts better clinical outcomes in multiple myeloma. BLR is significantly associated with established clinical markers of tumor burden in multiple myeloma. These findings suggest that BLR is a feasible and reproducible metric with potential prognostic value in multiple myeloma.

Indexed as

BrainFluorodeoxyglucose F18LiverMultiple MyelomaPositron Emission Tomography Computed TomographyAgedBiological TransportFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesSurvival AnalysisFluorodeoxyglucose F18[18F]FDG PET/CTBrain-to-liver ratioMultiple myelomaSUV

Identifiers

PMID41862725
PMCPMC13249654

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.