Evidence map›Paper›PMID 42398048›Full record

ArticleThe oncologist2026

The impact of relative dose intensity on pathological complete response in neoadjuvant chemotherapy of muscle-invasive urothelial cancer: a multicenter retrospective study.

Giuseppe Neola, Fabiano Flauto, Carmine Caso, Giuseppina Montuori, Marco Maruzzo, Eleonora Lai, Giuseppe Luigi Banna, Michele Maffezzoli, Mimma Rizzo, Francesco Massari and 16 more

Abstract readMulticenter Study
In one paragraph

Article in The oncologist, 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

26 authors.

Giuseppe NeolaDepartment of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, Naples, 80131, Italy.ORCID 0009-0009-2412-1310
Fabiano FlautoDepartment of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, Naples, 80131, Italy.ORCID 0009-0006-5699-4958
Carmine CasoDepartment of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, Naples, 80131, Italy.
Giuseppina MontuoriDepartment of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, Naples, 80131, Italy.
Marco MaruzzoOncology Unit 3, Istituto Oncologico Veneto - IOV IRCCS, Padova, 35128, Italy.
Eleonora LaiOncology Unit 3, Istituto Oncologico Veneto - IOV IRCCS, Padova, 35128, Italy.
Giuseppe Luigi BannaPortsmouth Hospitals University NHS Trust, Portsmouth, PO63LY, UK.ORCID 0000-0003-0764-3650
Michele MaffezzoliDepartment of Medicine and Surgery, University Hospital of Parma-Medical Oncology Unit, University of Parma, Parma, 43126, Italy.ORCID 0000-0001-7877-8988
Mimma RizzoMedical Oncology Unit, Azienda Ospedaliera Universitaria Consorziale Policlinico di Bari, Bari, 70124, Italy.
Francesco MassariMedical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, 40138, Italy.
Veronica MollicaMedical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, 40138, Italy.
Sarah ScagliariniUOC di Oncologia, Azienda Ospedaliera di Rilievo Nazionale Cardarelli di Napoli, Naples, 80131, Italy.
Vincenza ConteducaUnit of Medical Oncology and Biomolecular Therapy, Department of Medical and Surgical Sciences, University of Foggia, Policlinico Riuniti, 71122, Italy.ORCID 0000-0002-6921-714X
Patrizia GiannatempoGenitourinary Medical Oncology-Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, 80131, Italy.
Alessandro RamettaGenitourinary Medical Oncology-Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, 80131, Italy.
Brigida Anna MaioranoDepartment of Medical Oncology, IRCCS San Raffaele Hospital, Milan, 20132, Italy.
Gaetano FacchiniOncology Unit, S. Maria Delle Grazie Hospital, Pozzuoli, Naples, 80078, Italy.
Edoardo LenciMedical Oncology Unit, Azienda Ospedaliera Ospedali Riuniti Marche Nord, Pesaro, 61121, Italy.
Rosa TambaroUro-Gynecological Oncology, Istituto Nazionale Tumori-IRCCS-Fondazione G. Pascale, Naples, 80131, Italy.
Francesco GrilloneSOC Oncologia, PO Pugliese-Ciaccio, Azienda Ospedaliera Universitaria Renato Dulbecco, Catanzaro, 88100, Italy.
Davide BossoMedical Oncology Unit, Ospedale del Mare, Naples, 80147, Italy.ORCID 0009-0004-8045-3460
Felice CrocettoDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples Federico II, Naples, 80131, Italy.
Ciro ImbimboDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples Federico II, Naples, 80131, Italy.
Alberto ServettoDepartment of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, Naples, 80131, Italy.ORCID 0000-0003-3624-224X
Roberto BiancoDepartment of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, Naples, 80131, Italy.ORCID 0000-0003-3311-260X
Luigi FormisanoDepartment of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, Naples, 80131, Italy.ORCID 0000-0001-7205-5105

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCisplatin-based neoadjuvant chemotherapy (NAC) improves survival in muscle-invasive urothelial cancer (MIUC), yet pathological complete response (pCR) is achieved in a minority of patients. Relative dose intensity (RDI) is a potentially modifiable determinant of chemotherapy efficacy, but its impact during NAC in MIUC remains unexplored.

methodsThis multicenter retrospective study included patients with MIUC treated with cisplatin-gemcitabine NAC followed by radical cystectomy. Relative dose intensity was calculated from original administration records and categorized as ≥85% vs <85%. The primary endpoint was pCR (ypT0N0M0). Secondary endpoints included overall survival (OS) and event-free survival (EFS).

resultsA total of 330 patients were included; 66% maintained RDI ≥ 85%. Overall pCR rate was 25.2%. Patients with RDI ≥ 85% achieved higher pCR rates compared with those with RDI < 85% (29.7% vs 16.2%; P = .008). Relative dose intensity  ≥ 85% remained independently associated with pCR in multivariable analysis (odds ratio = 2.10; P = .032). Preserved RDI was also associated with improved EFS (hazard ratio [HR] = 0.65; P = .039) and OS (HR = 0.53; P = .026) at univariate analysis. Achievement of pCR was strongly associated with superior EFS (HR = 0.23; P < .001) and OS (HR = 0.35; P = .009).

conclusionPreservation of cisplatin RDI ≥ 85% during NAC is independently correlated with higher pCR rates and associated to a better survival trend in MIUC. Optimization of chemotherapy delivery represents a clinically actionable strategy to enhance neoadjuvant efficacy.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsNeoadjuvant TherapyUrinary Bladder NeoplasmsAgedCisplatinDeoxycytidineFemaleGemcitabineHumansMaleMiddle AgedPathologic Complete ResponseRetrospective StudiesCisplatinDeoxycytidineGemcitabinebladder cancerneoadjuvantpathological complete responserelative dose intensityurothelial cancer

Identifiers

PMID42398048
PMCPMC13395094

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.