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Radiofrequency-induced thermo-chemotherapy effect versus a second course of Bacillus Calmette-Guérin or institutional standard in patients with recurrence of non-muscle-invasive bladder cancer following induction or maintenance Bacillus Calmette-Guérin therapy (HYMN): A phase III, open-label, randomised controlled trial

  • Sanjeev Madaan
  • , Tan WS
  • , Panchal A
  • , Buckley L
  • , Devall AJ
  • , Loubière LS
  • , Pope AM
  • , Feneley
  • , Cresswell J
  • , Issa R
  • , Mostafid H
  • , Bhatt R
  • , McGrath J
  • , Sangar V
  • , Griffiths TRL
  • , Page T
  • , Hodgson D
  • , Datta SN
  • , Billingham LJ
  • , Kelly JD

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Background:
    There is no effective intravesical second-line therapy for non-muscle-invasive bladder cancer (NMIBC) when bacillus Calmette-Guérin (BCG) fails.


    Objective:
    To compare disease-free survival time (DFS) between radiofrequency-induced thermo-chemotherapy effect (RITE) and institutional standard second-line therapy (control) in NMIBC patients with recurrence following induction/maintenance BCG.

    Design, settings, and participants:
    Open-label, phase III randomised controlled trial accrued across 14 centres between May 2010 and July 2013 (HYMN [ClinicalTrials.gov: NCT01094964]).

    Intervention:
    Patients were randomly assigned (1:1) to RITE (60min, 40mg mitomycin-C, 42±2°C) or control following stratification for carcinoma in situ (CIS) status (present/absent), therapy history (failure of previous induction/maintenance BCG), and treatment centre.

    Outcome measurements and statistical analysis:
    Primary outcome measures were DFS and complete response (CR) at 3 mo for the CIS at randomisation subgroup. Analysis was based on intention-to-treat.

    Results and limitations:
    A total of 104 patients were randomised (48 RITE: 56 control). Median follow-up for the 31 patients without a DFS event was 36 mo. There was no significant difference in DFS between treatment arms (hazard ratio [HR] 1.33, 95% confidence interval [CI] 0.84-2.10, p=0.23) or in 3-mo CR rate in CIS patients (n=71; RITE: 30% vs control: 47%, p=0.15). There was no significant difference in DFS between treatment arms in non-CIS patients (n=33; RITE: 53% vs control: 24% at 24 mo, HR 0.50, 95% CI 0.22-1.17, p=0.11). DFS was significantly lower in RITE than in control in CIS with/without papillary patients (n=71; HR 2.06, 95% CI 1.17-3.62, p=0.01; treatment-subgroup interaction p=0.007). Disease progression was observed in four patients in each treatment arm. Adverse events and health-related quality of life between treatment arms were comparable.

    Conclusions:
    DFS was similar between RITE and control. RITE may be a second-line therapy for non-CIS recurrence following BCG failure; however, confirmatory trials are needed. RITE patients with CIS with/without papillary had lower DFS than control. HYMN highlights the importance of the control arm when evaluating novel therapies.

    Patient summary:
    This study did not show a difference in bladder cancer outcomes between microwave-heated chemotherapy and standard of care treatment. Papillary bladder lesions may benefit from microwave-heated chemotherapy treatment; however, more research is needed. Both treatments are similarly well tolerated.
    Original languageEnglish
    Pages (from-to)63-71
    JournalEuropean Urology
    Volume75
    Issue number1
    DOIs
    Publication statusPublished - 28 Sept 2019

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • BCG failure
    • Bladder cancer
    • Chemotherapy
    • Device-assisted therapy
    • Hyperthermia
    • Mitomycin-C;
    • Radiofrequency
    • Randomised controlled trial
    • Thermotherapy

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