Evidence map›Paper›PMID 39665773›Full record

Observational studyJMIR cancer2024

Correlation Between Electronic Patient-Reported Outcomes and Biological Markers of Key Parameters in Acute Radiation Cystitis Among Patients With Prostate Cancer (RABBIO): Prospective Observational Study.

Carole Helissey, Sophie Cavallero, Nathalie Guitard, Hélène Thery, Charles Parnot, Antoine Schernberg, Imen Aissa, Florent Raffin, Christine Le Coz, Stanislas Mondot and 6 more

Abstract readObservational Study
In one paragraph

Observational study in JMIR cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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

16 authors.

Carole HelisseyClinical Unit Research, Military Hospital Begin, 69 avenue de Paris, Saint-Mandé, 94240, France, 33 679526487.ORCID 0000-0002-7774-349X
Sophie CavalleroDepartment of Radiation Biological Effects, French Armed Forces Biomedical Research Institute, IRBA, Brétigny-sur-Orge, France.ORCID 0000-0001-6581-3369
Nathalie GuitardDepartment of Radiation Biological Effects, French Armed Forces Biomedical Research Institute, IRBA, Brétigny-sur-Orge, France.ORCID 0000-0002-6208-1147
Hélène TheryDepartment of Radiation Biological Effects, French Armed Forces Biomedical Research Institute, IRBA, Brétigny-sur-Orge, France.ORCID 0000-0002-3809-2516
Charles ParnotCureety, Dinan, France.ORCID 0000-0002-7346-5883
Antoine SchernbergClinical Unit Research, Military Hospital Begin, 69 avenue de Paris, Saint-Mandé, 94240, France, 33 679526487.ORCID 0000-0002-2513-4721
Imen AissaMEDIAXE, CLAMART, France.ORCID 0000-0003-2645-2948
Florent RaffinDepartment of Radiation Biological Effects, French Armed Forces Biomedical Research Institute, Brétigny-sur-Orge, France.ORCID 0000-0002-6532-5338
Christine Le CozDepartment of Radiation Biological Effects, French Armed Forces Biomedical Research Institute, Brétigny-sur-Orge, France.ORCID 0009-0004-6929-2889
Stanislas MondotParis-Saclay University, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.ORCID 0000-0003-3668-3168
Christos ChristopoulosDepartment of Radiotherapy, Le Raincy Montfermeil General Hospital, Montfermeil, France.ORCID 0009-0009-7018-9770
Karim MalekDepartment of Radiotherapy, Le Raincy Montfermeil General Hospital, Montfermeil, France.ORCID 0000-0003-2150-4024
Emmanuelle MalaurieDepartment of Radiotherapy, Centre Hospitalier Intercommunal de Créteil, Créteil, France.ORCID 0000-0003-0882-2167
Pierre BlanchardDepartment of Radiation Oncology, Gustave Roussy Cancer Campus, Université Paris-Saclay, Oncostat U1018 INSERM, Gustave-Roussy, Villejuif, France.ORCID 0000-0003-4785-3409
Cyrus ChargariDepartment of Radiation Oncology, Pitié Salpêtrière University Hospital, Paris, France.ORCID 0000-0003-0119-3695
Sabine FrancoisDepartment of Radiation Biological Effects, French Armed Forces Biomedical Research Institute, Brétigny-sur-Orge, France.ORCID 0000-0002-3193-6122

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Despite advances in radiation techniques, radiation cystitis (RC) remains a significant cause of morbidity from pelvic radiotherapy, which may affect patients' quality of life (QoL). The pathophysiology of RC is not well understood, which limits the development of effective treatments. Objective: The Radiotoxicity Bladder Biomarkers study aims to investigate the correlation between blood and urinary biomarkers and the intensity of acute RC symptoms and QoL in patients undergoing localized prostate cancer radiotherapy. Methods: This study included patients with low- or intermediate-risk localized prostate cancer who were eligible for localized radiotherapy. Blood and urinary biomarkers were analyzed before radiotherapy was initiated and at weeks 4 and 12 of radiation therapy. Patients completed questionnaires related to RC symptoms and QoL (International Prostate Symptom Score and Functional Assessment of Cancer Therapy-Prostate [FACT-P]) using a digital remote monitoring platform. The information was processed by means of an algorithm, which classified patients according to the severity of symptoms and adverse events reported. Levels of blood and urinary biomarkers were tested with the severity of acute RC symptoms and patient-reported QoL. Results: A total of 401 adverse events questionnaires were collected over the duration of this study from 20 patients. The most frequently reported adverse events at week 4 were pollakiuria, constipation, and diarrhea. In comparison with baseline, the mean FACT-P score decreased at week 4. A significant increase in the proportion of M2 phenotype cells (CD206+, CD163+, CD204+) at W12 compared to W0 was observed. An increase in serum and urine levels of macrophage colony-stimulating factor (M-CSF), hepatocyte growth factor, and macrophagic inflammatory protein was observed at week 12 compared to baseline levels. Baseline serum and urine M-CSF concentrations showed a significant negative correlation with FACT-P scores at weeks 4 and 12 (r=-0.65, P=.04, and r=-0.76, P=.02, respectively). Conclusions: The Radiotoxicity Bladder Biomarkers study is the first to explore the overexpression of inflammatory proteins in blood and urine of patients with symptoms of acute RC. These preliminary findings suggest that serum and urine levels of hepatocyte growth factor, M-CSF, and macrophagic inflammatory protein, as well as macrophage polarization, are mobilized after prostate radiotherapy. The elevated M-CSF levels in serum and urine at baseline were associated with the deterioration of QoL during radiotherapy. The results of this study may help to develop mitigation strategies to limit radiation damage to the bladder.

Indexed as

CystitisPatient Reported Outcome MeasuresProstatic NeoplasmsQuality of LifeRadiation InjuriesAgedBiomarkersHumansMaleMiddle AgedProspective StudiesSurveys and QuestionnairesBiomarkersacute radiation cystitisbiomarkerselectronic patient-reported outcomee-PROprostate cancerquality of life

Identifiers

PMID39665773
PMCPMC11656992

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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.