CTRI/2025/03/083504 [Registered on: 26/03/2025] Trial Registered Prospectively
Last Modified On:
13/03/2025
Post Graduate Thesis
No
Type of Trial
Observational
Type of Study
Cohort Study
Study Design
Other
Public Title of Study
Quality of Life and Survival between Surgery and Organ-Preservation Therapy in bladder cancer treatment
Scientific Title of Study
Quality of Life and Evaluation of
Survival in Treatment of Bladder Cancer
Trial Acronym
Secondary IDs if Any
Secondary ID
Identifier
NIL
NIL
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
Name
Dr Jayanta Chakrabarti
Designation
Director of Institute and Head of Surgical Oncology
Affiliation
Chittaranjan National Cancer Institute
Address
Director Office, Chittaranjan National Cancer Institute, 37 S P Mukherjee Road, Kolkata
Kolkata WEST BENGAL 700026 India
Phone
9836426866
Fax
Email
swayamjayanta@gmail.com
Details of Contact Person Scientific Query
Name
Dr Debjit Ghosh
Designation
Assistant Professor & Specialist Grade II
Affiliation
Chittaranjan National Cancer Institute
Address
Room no 25, Ground Floor, Department of Radiation Oncology, Chittaranjan National Cancer Institute, 37 S P Mukherjee Road, Kolkata Kolkata Kolkata WEST BENGAL 700026 India
Phone
7044690778
Fax
Email
debjitghosh15@gmail.com
Details of Contact Person Public Query
Name
Dr Debjit Ghosh
Designation
Assistant Professor & Specialist Grade II
Affiliation
Chittaranjan National Cancer Institute
Address
Room no 25, Ground Floor, Department of Radiation Oncology, Chittaranjan National Cancer Institute, 37 S P Mukherjee Road, Kolkata Kolkata Kolkata WEST BENGAL 700026 India
Phone
7044690778
Fax
Email
debjitghosh15@gmail.com
Source of Monetary or Material Support
Chittaranjan National Cancer Institute, 37 S P Mukherjee Road, Kolkata, West Bengal, India. PIN 700026
Primary Sponsor
Name
Chittaranjan National Cancer Institute
Address
Chittaranjan National Cancer Institute, 37 S P Mukherjee Road, Kolkata, West Bengal, India. PIN 700026
Type of Sponsor
Research institution and hospital
Details of Secondary Sponsor
Name
Address
NIL
NIL
Countries of Recruitment
India
Sites of Study
No of Sites = 1
Name of Principal
Investigator
Name of Site
Site Address
Phone/Fax/Email
Dr Debjit Ghosh
Chittaranjan National Cancer Institute
Chittaranjan National Cancer Institute, 37 S P Mukherjee Road, Kolkata Kolkata WEST BENGAL
07044690778
debjitghosh15@gmail.com
Details of Ethics Committee
No of Ethics Committees= 1
Name of Committee
Approval Status
Institutional Ethics Committee
Approved
Regulatory Clearance Status from DCGI
Status
Not Applicable
Health Condition / Problems Studied
Health Type
Condition
Patients
(1) ICD-10 Condition: C679||Malignant neoplasm of bladder, unspecified,
Intervention / Comparator Agent
Type
Name
Details
Comparator Agent
NIL
NIL
Intervention
NIL
NIL
Inclusion Criteria
Age From
18.00 Year(s)
Age To
80.00 Year(s)
Gender
Both
Details
Patients diagnosed with muscle-invasive bladder cancer (MIBC, cT2-T4aN0M0), eligible for both bladder preservation and radical cystectomy and giving informed consent to participate
ExclusionCriteria
Details
Patients with metastatic disease (M1) at presentation or having received prior pelvic irradiation or surgery affecting urinary/bowel function or patients unwilling to complete PROM questionnaires
Method of Generating Random Sequence
Not Applicable
Method of Concealment
Not Applicable
Blinding/Masking
Not Applicable
Primary Outcome
Outcome
TimePoints
To compare quality of life (QoL) outcomes between bladder preservation and radical cystectomy patients using validated PROM tools namely Bladder Cancer Index (BCI) & EORTC QLQ-C30
At 3 months, 6 months, 9 months, 12 months and thereafter annually all relevant follow up data and filled PROM questionnaires shall be collected, till completion of this study.
Secondary Outcome
Outcome
TimePoints
To assess overall survival (OS) and progression-free survival (PFS) of patients undergoing bladder preservation versus radical cystectomy & to correlate PROM-derived QoL scores with survival outcomes.
At 3 months, 6 months, 9 months, 12 months and thereafter annually all relevant follow up data and filled PROM questionnaires shall be collected, till completion of this study.
Target Sample Size
Total Sample Size="140" Sample Size from India="140" Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials" Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials"
Phase of Trial
N/A
Date of First Enrollment (India)
01/04/2025
Date of Study Completion (India)
Applicable only for Completed/Terminated trials
Date of First Enrollment (Global)
Date Missing
Date of Study Completion (Global)
Applicable only for Completed/Terminated trials
Estimated Duration of Trial
Years="3" Months="0" Days="0"
Recruitment Status of Trial (Global)
Not Yet Recruiting
Recruitment Status of Trial (India)
Not Yet Recruiting
Publication Details
N/A
Individual Participant Data (IPD) Sharing Statement
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - YES
What data in particular will be shared? Response - All of the individual participant data collected during the trial, after de-identiļ¬cation.
What additional supporting information will be shared? Response - Study Protocol Response - Statistical Analysis Plan Response - Informed Consent Form Response - Clinical Study Report Response - Analytic Code
Who will be able to view these files? Response - Anyone
For what types of analyses will this data be available? Response - Any purpose.
By what mechanism will data be made available? Response - Proposals should be directed to [debjitghosh15@gmail.com].
For how long will this data be available start date provided 01-08-2028 and end date provided 01-08-2033? Response - Beginning 3 months and ending 5 years following article publication.
Any URL or additional information regarding plan/policy for sharing IPD? Additional Information - NIL
Brief Summary
A Prospective Study on QoL and Survival of Bladder Cancer Patients Using Patient-Reported Outcome Measurements PROMs
Principal Investigator Dr. Jayanta Chakrabarti
Co-Investigators Dr. Ranti Ghosh, Dr. Debarshi Lahiri, Dr. Tapas Maji, Dr. Debjit Ghosh
Background and Rationale
Bladder cancer is one of the most common malignancies worldwide, with muscle-invasive bladder cancer MIBC constituting approximately 25 to 30 percent of newly diagnosed cases. MIBC stage T2-T4a poses a significant clinical challenge, as it requires multimodal treatment strategies to achieve optimal oncological control and maintain quality of life QoL.
Evolution of MIBC Management
Historically, neoadjuvant chemotherapy followed by radical cystectomy RC emerged as the cornerstone of curative treatment for MIBC. Introduced in the early 20th century, radical cystectomy involves removal of the bladder, surrounding organs, and lymph nodes, often accompanied by urinary diversion procedures such as ileal conduit, continent cutaneous diversion, or neobladder reconstruction. While RC provides effective local control and long-term survival, it is associated with significant perioperative morbidity, impact on urinary and sexual function, and deterioration in overall QoL.
Over the past few decades, there has been a paradigm shift towards bladder preservation strategies, driven by advancements in multidisciplinary oncology care. Bladder preservation typically involves trimodal therapy TMT, which combines
Maximal transurethral resection of bladder tumor TURBT
Concurrent chemoradiotherapy CRT
Meticulous surveillance to detect recurrence or progression
This approach gained traction following landmark studies demonstrating comparable oncological outcomes between bladder preservation and radical cystectomy in well-selected patients. The development of modern radiotherapy techniques, such as image-guided radiotherapy IGRT and intensity-modulated radiotherapy IMRT, has further improved tumor control while minimizing radiation toxicity to adjacent normal tissues. Concurrently, systemic therapies such as gemcitabine-based or cisplatin-based chemotherapy regimens have enhanced the radiosensitizing effects, improving the efficacy of bladder preservation approaches.
Bladder Preservation versus Radical Cystectomy The QoL Perspective
While survival and disease progression outcomes for TMT and RC are now considered equivalent in selected patients, their impact on QoL is markedly different. Radical cystectomy, despite being curative, often leads to profound changes in urinary, bowel, and sexual function due to the absence of the native bladder and the need for urinary diversion. Conversely, bladder preservation aims to maintain the natural bladder, thereby preserving functional outcomes and improving QoL for many patients.
Several studies, including an Indian study, have compared QoL between the two modalities using validated Patient-Reported Outcome Measures PROMs such as the Bladder Cancer Index BCI and the EORTC QLQ-C30. These studies consistently demonstrate that bladder preservation offers superior QoL, particularly in the domains of urinary function, bowel function, and sexual health. However, such data remain limited in the Indian context, where treatment decisions are influenced by socioeconomic, cultural, and logistical factors.
Need for the Current Study
Given the rising burden of bladder cancer and the increasing adoption of bladder preservation strategies, there is a need for institution-specific data to guide clinical decision-making. At our tertiary care cancer center in eastern India, we manage a substantial number of MIBC patients annually. While previous studies have provided valuable insights into QoL outcomes, there is limited evidence integrating QoL metrics with survival outcomes in a prospective cohort.
Given the large volume of bladder cancer patients treated annually at our center, there is a unique opportunity to replicate this study while also integrating survival outcomes with patient-reported QoL metrics. This will help establish institution-specific data to guide treatment planning and shared decision-making tailored to our patient population.
Objectives
Primary Objective
To compare quality of life QoL outcomes between bladder preservation and radical cystectomy patients using validated PROM tools
Bladder Cancer Index BCI
EORTC QLQ-C30
Secondary Objectives
To assess overall survival OS and progression-free survival PFS of patients undergoing bladder preservation versus radical cystectomy
To correlate PROM-derived QoL scores with survival outcomes
Methods
Study Design
A prospective observational cohort study.
Study Population
Inclusion Criteria
Patients diagnosed with muscle-invasive bladder cancer MIBC, cT2-T4aN0M0
Patients eligible for both bladder preservation and radical cystectomy
Age 18 years or older
Informed consent to participate
Exclusion Criteria
Patients with metastatic disease M1 at presentation
Prior pelvic irradiation or surgery affecting urinary or bowel function
Patients unwilling to complete PROM questionnaires
Sample Size
Based on the institutional annual caseload of bladder cancer and the expected response rates for PROMs, a total of n patients will be recruited over a 12-month enrollment period.
Study Groups
Patients will be stratified into two groups based on their treatment choice guided by informed consent forms in their mother tongue, explaining the pros and cons of each choice of modality
Group 1 Bladder preservation TURBT plus chemoradiation
Group 2 Neoadjuvant chemotherapy followed by radical cystectomy with or without adjuvant therapy
Study Tools
Bladder Cancer Index BCI A validated PROM tool measuring urinary, bowel, and sexual QoL domains
EORTC QLQ-C30 A global cancer QoL tool assessing functional, symptom, and global health status scales
Note The institution has secured the license to use BCI from the University of Michigan. Translations into local vernacular languages will be validated prior to use.
Follow-Up Intervals PROM assessments will be performed at 3 months 6 months 12 months Thereafter annually
Survival Data Overall survival and progression-free survival will be monitored at regular clinical follow-ups.
Statistical Analysis
Descriptive Statistics Mean, median, and standard deviation for QoL scores
Inferential Statistics Comparison of QoL between groups using t-tests or Mann-Whitney U tests. Kaplan-Meier curves for OS and PFS analysis. Cox proportional hazards regression to evaluate the correlation between QoL scores and survival outcomes
Software IBM SPSS version 25
Ethical Considerations
Ethics Approval The study will be submitted for approval to the Institutional Ethics Committee IEC
Informed Consent Written informed consent will be obtained from all participants after providing detailed information about the study
Confidentiality Patient data will be anonymized and stored securely in password-protected systems
PROM Tools Local vernacular translations will be validated as per standard protocols to ensure cultural appropriateness and linguistic accuracy
Timeline
Phase
Duration
IEC Approval and Study Setup
2 months
Participant Recruitment
12 months
Follow-up and Data Collection
12 months
Data Analysis and Manuscript
6 months
Total Study Duration Approximately 3 years
Expected Outcomes
A comprehensive comparison of QoL outcomes between bladder preservation and radical cystectomy in our patient population
Institution-specific survival data correlated with PROM-derived QoL scores
Insights to inform patient counseling, shared decision-making, and treatment planning