Evidence map›Paper›PMID 40163089›Full record

ArticleStrahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]2025

Association of long-term treatment outcomes with changes in PET/MRI characteristics and the type of early treatment response during concurrent radiochemotherapy in patients with locally advanced cervical cancer.

Radovan Vojtíšek, Jan Baxa, Petr Hošek, Petra Kovářová, Martin Vítovec, Emília Sukovská, Jan Kosťun, Pavel Vlasák, Jiří Presl, Jiří Ferda and 1 more

Abstract read
In one paragraph

Article in Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al], 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. 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

11 authors.

Radovan VojtíšekFaculty of Medicine, Charles University, Pilsen, Czech Republic. vojtisekr@fnplzen.cz.ORCID 0000-0001-7318-7927
Jan BaxaDepartment of Imaging Methods, University Hospital in Pilsen, alej Svobody 80, 304 60, Pilsen, Czech Republic.
Petr HošekBiomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 76, 323 00, Pilsen, Czech Republic.
Petra KovářováDepartment of Oncology and Radiotherapy, University Hospital in Pilsen, alej Svobody 80, 304 60, Pilsen, Czech Republic.
Martin VítovecDepartment of Imaging Methods, University Hospital in Pilsen, alej Svobody 80, 304 60, Pilsen, Czech Republic.
Emília SukovskáDepartment of Oncology and Radiotherapy, University Hospital in Pilsen, alej Svobody 80, 304 60, Pilsen, Czech Republic.
Jan KosťunDepartment of Gynecology and Obstetrics, University Hospital in Pilsen, alej Svobody 80, 304 60, Pilsen, Czech Republic.
Pavel VlasákDepartment of Gynecology and Obstetrics, University Hospital in Pilsen, alej Svobody 80, 304 60, Pilsen, Czech Republic.
Jiří PreslDepartment of Gynecology and Obstetrics, University Hospital in Pilsen, alej Svobody 80, 304 60, Pilsen, Czech Republic.
Jiří FerdaDepartment of Imaging Methods, University Hospital in Pilsen, alej Svobody 80, 304 60, Pilsen, Czech Republic.
Jindřich FínekDepartment of Oncology and Radiotherapy, University Hospital in Pilsen, alej Svobody 80, 304 60, Pilsen, Czech Republic.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe aimed to find predictive tumour characteristics as detected by interim positron-emission tomography/magnetic resonance imaging (PET/MRI) in cervical cancer patients. We also investigated the type of interim response. Furthermore, we compared the investigated parameters with disease-free (DFS) and overall survival (OS) outcomes.

methodsWe evaluated 108 patients treated between August 2015 and January 2023 with external-beam radiotherapy (EBRT) and image-guided adaptive brachytherapy (IGABT) who had undergone pretreatment staging, subsequent mid-treatment evaluation after completed EBRT and definitive restaging 3 months after completing the whole treatment using PET/MRI. Patients were then divided into two groups based on the RECIST and PERCIST criteria: responders (achieving complete metabolic response, CMR) and non-responders (non-CMR). These two groups were compared using selected parameters obtained at pre-PET/MRI and mid-PET/MRI. The early response to treatment as evaluated by mid-PET/MRI was categorized into three types: interim complete metabolic response, interim nodal response and interim nodal persistence.

resultsMid-TLG‑S (the sum of total lesion glycolysis for the primary tumour plus pelvic and para-aortic lymph nodes) parameter showed the best discriminatory ability for predicting non-CMR. The second factor with significant discriminatory ability was mid-MTV‑S (the sum of the metabolic tumour volume of the primary tumour plus pelvic and para-aortic lymph nodes). The strongest factor, mid-TLG‑S, showed a sensitivity of 40% and a specificity of 90% at a threshold value of 70. We found a statistically significant association of DFS and OS with the following parameters: number of chemotherapy cycles, early response type and CMR vs. non-CMR.

conclusionWe were able to identify thresholds for selected parameters that can be used to identify patients who are more likely to have worse DFS and OS. The type of early response during concurrent chemoradiotherapy (CCRT) was also significantly associated with DFS and OS. These aspects represent an important contribution to the possible stratification of patients for subsequent individualised adjuvant treatment.

Indexed as

ChemoradiotherapyMagnetic Resonance ImagingMultimodal ImagingPositron-Emission TomographyUterine Cervical NeoplasmsAdultAgedBrachytherapyDisease-Free SurvivalFemaleHumansMiddle AgedNeoplasm StagingRadiotherapy, Image-GuidedTreatment OutcomeBrachytherapyMagnetic resonance imagingPositron-emission tomographySurvivalUterine cervical neoplasms

Identifiers

PMID40163089
PMCPMC12014719

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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.