Intravesical Thermochemotherapy With Mitomycin-c

NCT ID: NCT03694535

Last Updated: 2018-10-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

44 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-01-01

Study Completion Date

2017-09-15

Brief Summary

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To investigate effect of intravesical mitomycin-C(MMC) applied with bladder wall thermotherapy system on reccurrence and progression status of intermediate and high risk non muscle invasive bladder cancer

Detailed Description

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Before the application of TCT, complete transurethral bladder tumour resection (TURBT) was performed. RE-TURBT was conducted within 4 weeks for patients with initial T1 pathology. The first TCT instillation was applied at 1mo following the TURBT or the RE-TURBT.

Thermochemotherapy application and treatment schedule:

The bladder wall TCT (BWT) system (Elmedical Ltd, Hod-Hasharon, Israel) was used as a conductive heating modality. MMC (40 mg; MMC Kyowa Hakko Kogyo Co., Ltd., Tokyo, Japan) was mixed with 50 mL of 0.9% saline solution and applied using a disposable silicone 20Fr 3-way TCT catheter (UniThermia catheter; Elmedical Ltd). In each session, the bladder was irrigated with MMC solution at 42°C-45°C for 45 min via the BWT system. The treatment schedule consisted of an initial 6-week instillation, followed by control cystoscopy and urine cytology in the 3rd month and monthly instillations up to 1 yr. Urine cytology and cystoscopy were performed every three months. The samples were collected from the suspected areas during cystoscopy. At the end of the first year, control cystoscopy with random bladder biopsies was conducted. During the second year, routine controls were conducted every three months. Subsequently, follow-ups were performed every six months. In case of development of any complication in a patient, TCT was discontinued. Before each instillation of TCT, clear urine cultures were obtained from all patients. No prophylactic anticholinergic was administered prior to intravesical TCT. If TUR BT pathology was Ta or T1 during the follow-up, it was accepted as a recurrence. If it was CIS or T2, it was accepted as a progression. All adverse events observed during the study were recorded according to the Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0 \[9. All study protocols were approved by the local ethical committee at our institution. An informed consent was obtained from all patients.

Conditions

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Bladder Cancer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

single group of patients composed of intermediate and high risk non muscle invasive bladder cancer
Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Bladder wall thermochemotherapy

Mitomycin-C application with bladder wall thermochemotherapy system after TUR bladder tumor in intermediate and high risk non muscle invasive bladder cancer

Group Type EXPERIMENTAL

bladder wall thermotherapy with Mitomycin-c

Intervention Type DRUG

application of intravesical mitomycin-C with hyperthermia

Interventions

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bladder wall thermotherapy with Mitomycin-c

application of intravesical mitomycin-C with hyperthermia

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* newly diagnosed or followed as recurrent intermediate-risk non muscle invasive non muscle invasive bladder cancer according to the criteria of European Association of Urology.
* newly diagnosed or followed as recurrent high-risk non muscle invasive non muscle invasive bladder cancer according to the criteria of European Association of Urology.
* pathology of urothelial carcinoma

Exclusion Criteria

* Low bladder capacity (\<150ml)
* increased post voiding residual urine (\>150ml)
* untreatable or uncontrollable urinary tract infection
* history of urethral stricture
* presence of bladder diverticula larger than 1 cm
* pathology other than urothelial carcinoma
* WHO (World Health Organization) performance status \> 2
* upper urinary tract urothelial carcinoma diagnosis
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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TC Erciyes University

OTHER

Sponsor Role lead

Responsible Party

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Abdullah Demirtas

Md, Assoc. Prof.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Abdullah Demirtas, MD

Role: PRINCIPAL_INVESTIGATOR

TC Erciyes University Medical Faculty

Locations

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Department of Urology, Ercieys University, Faculty Of Medicine,

Kayseri, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Moskovitz B, Meyer G, Kravtzov A, Gross M, Kastin A, Biton K, Nativ O. Thermo-chemotherapy for intermediate or high-risk recurrent superficial bladder cancer patients. Ann Oncol. 2005 Apr;16(4):585-9. doi: 10.1093/annonc/mdi124. Epub 2005 Feb 25.

Reference Type BACKGROUND
PMID: 15734775 (View on PubMed)

Colombo R, Salonia A, Leib Z, Pavone-Macaluso M, Engelstein D. Long-term outcomes of a randomized controlled trial comparing thermochemotherapy with mitomycin-C alone as adjuvant treatment for non-muscle-invasive bladder cancer (NMIBC). BJU Int. 2011 Mar;107(6):912-8. doi: 10.1111/j.1464-410X.2010.09654.x. Epub 2010 Oct 4.

Reference Type BACKGROUND
PMID: 21029314 (View on PubMed)

Other Identifiers

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2014/387

Identifier Type: -

Identifier Source: org_study_id

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