Hyperthermic Mitomycin C in Intermediate-risk Non-muscle-invasive Bladder Cancer: Results of the HIVEC-1 Trial

dc.contributor.authorAngulo Cuesta, Javier
dc.contributor.authorÁlvarez Ossorio, José L.
dc.contributor.authorDomínguez Escrig, José L.
dc.contributor.authorMoyano, J. L.
dc.contributor.authorSousa, Alejandro
dc.contributor.authorFernández Gómez, Jesús María
dc.contributor.authorGómez Veiga, Francisco
dc.contributor.authorUnda, Miguel
dc.contributor.authorCarballido Rodríguez, Joaquín
dc.contributor.authorPalou, Joan
dc.contributor.authorEt al.
dc.date.accessioned2023-12-15T20:05:29Z
dc.date.available2023-12-15T20:05:29Z
dc.date.issued2023
dc.description.abstractBackground: Optimising therapeutic strategies of intermediate-risk non-muscle-invasive bladder cancer (IR-NMIBC) is needed. Objective: To compare recurrence-free survival (RFS) with adjuvant intravesical mitomycin C (MMC) at normothermia or hyperthermia using the COMBAT bladder recirculation system at 43 °C for 30 and 60 min. Design, setting, and participants: A prospective open-label, phase 3 randomised controlled trial (HIVEC-1) accrued across 13 centres between 2014 and 2020 in Spain. After complete transurethral resection of the bladder and immediate postoperative MMC instillation, patients with IR-NMIBC were randomised (1:1:1) to four weekly followed by three monthly 40-mg MMC instillations at normothermia (control; n = 106), 43 °C for 30 min (n = 107), or 43 °C for 60 min (n = 106) were investigated. Therapeutic compliance was defined as four or more instillations. Outcome measurements and statistical analysis: The primary outcome was RFS at 24 mo in the intention-to-treat (ITT) and per-protocol (PP) populations. The secondary outcomes included progression-free survival at 24 mo, safety outcome measures, and changes in health-related quality of life. Log-rank, Fisher, χ2, and analysis of variance tests were used. Results and limitations: The ITT 24-mo RFS was 77% for control, 82% for 43 °C-30 min, and 80% for 43 °C-60 min (p = 0.6). The PP 24-mo RFS was 77% for control, 83% for 43 °C-30 min, and 80% for 43 °C-60 min (p = 0.59). Six patients progressed to muscle-invasive disease in the ITT population (four in the control, 43 °C-30 min, and 43 °C-60 min groups each) and four in the PP population (all controls). Serious adverse events occurred in 26 patients (8.1%), and we were unable to demonstrate a difference between groups (p = 0.5). Adverse events, mainly dysuria and spasms, occurred in 124 patients (33% in control, 35% in 43 °C-30 min, and 48% in 43 °C-60 min; p = 0.05). The total International Prostate Symptom Score worsened by 1.2 ± 7.3 points, similarly across groups (p = 0.29). The Functional Assessment of Cancer Therapy-Bladder domains and indexes showed no significant change. Conclusions: Four-month adjuvant hyperthermic MMC using the COMBAT system for 30 and 60 min in IR-NMIBC is well tolerated, but we did not find it to be superior to normothermic MMC at 24 mo.spa
dc.description.filiationUEMspa
dc.description.impact8.3 Q1 JCR 2023spa
dc.description.impact2.719 Q1 SJR 2023spa
dc.description.impactNo data IDR 2023spa
dc.description.sponsorshipSin financiaciónspa
dc.identifier.citationAngulo, J. C., Álvarez-Ossorio, J. L., Domínguez-Escrig, J. L., Moyano, J. L., Sousa, A., Fernández, J. M., Gómez-Veiga, F., Unda, M., Carballido, J., Carrero, V., Fernandez-Aparicio, T., García de Jalón, Á., Solsona, E., Inman, B., & Palou, J. (2023). Hyperthermic Mitomycin C in Intermediate-risk Non-muscle-invasive Bladder Cancer: Results of the HIVEC-1 Trial. European Urology Oncology, 6(1), 58–66. https://doi.org/10.1016/j.euo.2022.10.008spa
dc.identifier.doi10.1016/j.euo.2022.10.008
dc.identifier.issn2588-9311
dc.identifier.urihttp://hdl.handle.net/11268/12453
dc.language.isoengspa
dc.peerreviewedSispa
dc.relation.publisherversionhttps://doi.org/10.1016/j.euo.2022.10.008spa
dc.rights.accessRightsrestricted accessspa
dc.subject.otherNeoplasias de la próstataspa
dc.subject.unescoCáncerspa
dc.subject.unescoTratamiento médicospa
dc.titleHyperthermic Mitomycin C in Intermediate-risk Non-muscle-invasive Bladder Cancer: Results of the HIVEC-1 Trialspa
dc.typejournal articlespa
dspace.entity.typePublication
relation.isAuthorOfPublicationeaadbb3a-67c4-43f5-b477-5fb2318b809a
relation.isAuthorOfPublication.latestForDiscoveryeaadbb3a-67c4-43f5-b477-5fb2318b809a

Files