Evidence map›Paper›PMID 26025244›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2015

Could semiquantitative FDG analysis add information to the prognosis in patients with stage II/III breast cancer undergoing neoadjuvant treatment?

Laura Evangelista, Anna Rita Cervino, Cristina Ghiotto, Tania Saibene, Silvia Michieletto, Bozza Fernando, Enrico Orvieto, Valentina Guarneri, Pierfranco Conte

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In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. La Radiologia medica · 2025
    Article
  3. Review
  4. Comparison of MRI vs. [Journal of clinical medicine · 2023
    Review
  5. Article
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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 at 3 institutions in 1 country.

Laura EvangelistaRadiotherapy and Nuclear Medicine Unit, Veneto Institute of Oncology IOV - IRCCS, Via Gattamelata, 64, 35128, Padua, Italy. laura.evangelista@ioveneto.it.
Anna Rita CervinoRadiotherapy and Nuclear Medicine Unit, Veneto Institute of Oncology IOV - IRCCS, Via Gattamelata, 64, 35128, Padua, Italy.
Cristina GhiottoMedical Oncology 2 Unit, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Tania SaibeneBreast Unit, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Silvia MichielettoBreast Unit, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Bozza FernandoBreast Unit, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Enrico OrvietoDepartment of Pathology, University Hospital of Padua, Padua, Italy.
Valentina GuarneriMedical Oncology 2 Unit, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Pierfranco ConteMedical Oncology 2 Unit, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Istituti di Ricovero e Cura a Carattere Scientifico · ITIstituto Oncologico Veneto · ITUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe investigated whether maximum standardized uptake value (SUVmax), metabolic tumour volume (MTV), total lesion glycolysis (TLG) and whole-body (WB) SUVmax, WB MTV and WB TLG measured by (18)F-FDG PET/CT could improve prognostic stratification in patients with stage II/III breast cancer (BC).

methodsWe prospectively enrolled 99 consecutive women (median age 50 years, range 27 - 77 years) with pathologically proven stage II/III BC who underwent pretreatment FDG PET/CT. WB SUVmax, WB MTV and WB TLG were measured in all malignant lesions. Survival was analysed using the Kaplan-Meier method. Cox proportional hazards models were constructed to test for relationships among WB SUVmax, WB MTV, WB TLG, and overall survival (OS) and disease-free survival (DFS), after adjustment for age, and histopathological and immunohistochemical features (oestrogen/progesterone and HER2 expression, proliferation index and grade).

resultsThe median values of WB SUVmax, WB MTV and WB TLG were 16.2 (range 1.5 - 33.1), 14 cm(3) (range 0.03 - 708.6 cm(3)) and 62.5 (0.06 - 3869.4), respectively. All WB semiquantitative values were higher in patients with higher TNM stage, although not significantly (all p > 0.05). The median follow-up for surviving patients was 30 months, with a range of 13 - 45 months. Both PFS and OS of patients with low WB SUVmax, WB MTV and WB TLG were longer than that of patients with high WB values for progression, although not statistically significant. However, stratifying the patients in accordance with the stage of disease, both PFS and OS were significantly lower in patients with high WB TLG and stage III than in patients with stage II (p < 0.05). In multivariate analyses, WB MTV and WB TLG were independent prognostic factors for PFS (hazard ratio 1.004, 95% confidence interval 1.002 - 1.006, p < 0.001, and hazard ratio 1.001, 95% confidence interval 1.000 - 1.001, p = 0.011, respectively).

conclusionThe addition of WB TLG to clinical data may provide a more detailed prediction of outcome in patients with stage III BC. Moreover, WB MTV and WB TLG are independent factors predicting recurrence of BC. On the contrary, WB SUVmax has poor prognostic significance in this cohort of patients.

Indexed as

Fluorodeoxyglucose F18Neoadjuvant TherapyAdultAgedBreast NeoplasmsDisease-Free SurvivalFemaleHumansMiddle AgedMultimodal ImagingNeoplasm StagingPositron-Emission TomographyRetrospective StudiesTomography, X-Ray ComputedFluorodeoxyglucose F18

Identifiers

PMID26025244
OpenAlexW854484239

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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.