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Adjuvant Radiotherapy After Cystectomy for Muscle Invasive Bladder Cancer

Primary Purpose

Toxicity

Status
Active
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Adjuvant EBRT
Sponsored by
University Hospital, Ghent
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Toxicity focused on measuring assessment of QOL (EORTC QLQ-C30)

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: muscle invasive bladder cancer with:

  • ≥ pathological tumor stage (p)T3 stage + presence of lymphovascular invasion on pathological examination
  • pT4
  • <10 lymph nodes removed
  • positive lymph nodes
  • positive surgical margins

Exclusion Criteria:

-

Sites / Locations

  • Dept of Radiotherapy, University Hospital Ghent

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Adjuvant EBRT

Arm Description

Radiation up to a median dose of 50 Gy in 25 fractions will be delivered with IMAT to the pelvic lymph node regions. If there is a positive surgical margin, the operative bladder bed will be included in the radiation field. A simultaneous integrated boost to positive lymph nodes will be delivered.

Outcomes

Primary Outcome Measures

change from baseline in acute Radiation Therapy Oncology Group (RTOG) toxicity

Secondary Outcome Measures

change from baseline in late RTOG toxicity
change from baseline in local control
disease free survival
overall survival

Full Information

First Posted
November 19, 2014
Last Updated
October 19, 2023
Sponsor
University Hospital, Ghent
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1. Study Identification

Unique Protocol Identification Number
NCT02397434
Brief Title
Adjuvant Radiotherapy After Cystectomy for Muscle Invasive Bladder Cancer
Official Title
Adjuvant Radiotherapy After Cystectomy for Patients With Muscle Invasive Bladder Cancer: a Phase II Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 1, 2014 (Actual)
Primary Completion Date
October 30, 2018 (Actual)
Study Completion Date
October 30, 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Ghent

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
A radical cystectomy + extended pelvic lymph node dissection is considered to be the treatment of choice for patients with muscle invasive bladder cancer (MIBC). Despite this aggressive treatment the outcome is poor and ultimately, 30% of the patients with ≥pT3 tumors develop a pelvic recurrence. One- and 2-years survival for patients developing a local recurrence after cystectomy is only 8% and 3% respectively, with a median survival of <4 months. For patients with lymph node recurrence prognosis is somewhat better, but nevertheless still disappointing with reported 1- and 2 years survival of 42% and 11% respectively. The investigators hypothesize that an earlier implementation of external beam radiotherapy (EBRT) i.e. in the adjuvant setting, will prevent local and lymph node recurrence and improve disease free- and overall survival as local recurrence is linked to the development of distant metastasis. Adjuvant EBRT was tested in a prospective randomized trial and resulted in a 20% increase in 5-year disease free survival. Despite those impressive results, severe intestinal toxicity rates hampered the enthusiasm to use adjuvant EBRT, till now. In the last decade, great technological advancements in EBRT planning, such as intensity modulated arc therapy (IMAT), and positioning have been realised. This has resulted in a better coverage of the target volume while sparing normal tissue (mainly small bowel) and in a more precise delivery of the EBRT. Therefore, it is desirable to reconsider the use of adjuvant EBRT in selected MIBC patients.
Detailed Description
The investigators plan to perform a prospective phase 2 study including 76 patients. Radiation up to a median dose of 50 Gy in 25 fractions will be delivered with IMAT to the pelvic lymph node regions. If there is a positive surgical margin, the operative bladder bed will be included in the radiation field. A simultaneous integrated boost to 64 Gy to the positive lymph nodes will be delivered. Pathological evaluation on cystectomy specimen includes: tumor stage and grade, area of necrosis (absolute and relative), micro vessel density, epidermal growth factor receptor.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Toxicity
Keywords
assessment of QOL (EORTC QLQ-C30)

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
76 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Adjuvant EBRT
Arm Type
Experimental
Arm Description
Radiation up to a median dose of 50 Gy in 25 fractions will be delivered with IMAT to the pelvic lymph node regions. If there is a positive surgical margin, the operative bladder bed will be included in the radiation field. A simultaneous integrated boost to positive lymph nodes will be delivered.
Intervention Type
Radiation
Intervention Name(s)
Adjuvant EBRT
Intervention Description
Radiation up to a median dose of 50 Gy in 25 fractions will be delivered with IMAT to the pelvic lymph node regions. If there is a positive surgical margin, the operative bladder bed will be included in the radiation field. A simultaneous integrated boost to positive lymph nodes will be delivered.
Primary Outcome Measure Information:
Title
change from baseline in acute Radiation Therapy Oncology Group (RTOG) toxicity
Time Frame
last day of radiotherapy, 1 month and 3 months after last day of EBRT
Secondary Outcome Measure Information:
Title
change from baseline in late RTOG toxicity
Time Frame
at 6,9, 12, 18 and 24months after last day of EBRT
Title
change from baseline in local control
Time Frame
at 6,9, 12, 18 and 24months after last day of EBRT
Title
disease free survival
Time Frame
at 6,9, 12, 18 and 24months after last day of EBRT
Title
overall survival
Time Frame
at 6,9, 12, 18 and 24months after last day of EBRT

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: muscle invasive bladder cancer with: ≥ pathological tumor stage (p)T3 stage + presence of lymphovascular invasion on pathological examination pT4 <10 lymph nodes removed positive lymph nodes positive surgical margins Exclusion Criteria: -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Valérie Fonteyne
Organizational Affiliation
University Hospital, Ghent
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dept of Radiotherapy, University Hospital Ghent
City
Ghent
ZIP/Postal Code
9000
Country
Belgium

12. IPD Sharing Statement

Citations:
PubMed Identifier
28464906
Citation
Fonteyne V, Dirix P, Junius S, Rammant E, Ost P, De Meerleer G, Swimberghe M, Decaestecker K. Adjuvant radiotherapy after radical cystectomy for patients with muscle invasive bladder cancer: a phase II trial. BMC Cancer. 2017 May 2;17(1):308. doi: 10.1186/s12885-017-3302-9.
Results Reference
derived

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Adjuvant Radiotherapy After Cystectomy for Muscle Invasive Bladder Cancer

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