Trial of Neoadjuvant Intensity-Modulated Radiation Therapy Followed by Surgery and Intraoperative Radiation Therapy in Resectable Retroperitoneal Soft Tissue Sarcoma (RETRO-WTS)
Primary Purpose
Retroperitoneal Soft Tissue Sarcoma
Status
Completed
Phase
Phase 1
Locations
Germany
Study Type
Interventional
Intervention
Neoadjuvant intensity-modulated radiation therapy (IMRT)
intraoperative radiation therapy (IORT)
Sponsored by
About this trial
This is an interventional treatment trial for Retroperitoneal Soft Tissue Sarcoma focused on measuring retroperitoneal soft tissue sarcoma, IMRT, IORT
Eligibility Criteria
Inclusion Criteria:
- written informed consent
- histologically confirmed, primary or locally recurrent soft tissue sarcoma of the retroperitoneal space
- judged as at least marginally resectable
- absence of distant metastases
- tumor size ≥ 5 cm
Exclusion Criteria:
- missing written informed consent
- missing histological confirmation of soft tissue sarcoma
- Desmoid tumor (syn. aggressive fibromatosis)
- judged as gross incomplete or not resectable
- incomplete staging
- presence of distant metastases
- prior radiation therapy to the abdominal region
- participation in another clinical interventional study
- inflammatory bowel disease
Sites / Locations
- University Hospital Heidelberg
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
A
Arm Description
Neoadjuvant Intensity-Modulated Radiation Therapy Followed by Surgery and Intraoperative Radiation Therapy in Resectable Retroperitoneal Soft Tissue Sarcoma
Outcomes
Primary Outcome Measures
Local Control Rate
Secondary Outcome Measures
Progression free survival
Overall Survival
Acute toxicity
scored according to CTCAE 3.0
Late Toxicity
scored according to CTCAE 3.0 and RTOG criteria
Severe acute gastrointestinal toxicity
severe defined as grade >= III, scored according to CTC AE 3.0
Full Information
NCT ID
NCT01566123
First Posted
March 20, 2012
Last Updated
April 2, 2020
Sponsor
University Hospital Heidelberg
Collaborators
German Cancer Research Center
1. Study Identification
Unique Protocol Identification Number
NCT01566123
Brief Title
Trial of Neoadjuvant Intensity-Modulated Radiation Therapy Followed by Surgery and Intraoperative Radiation Therapy in Resectable Retroperitoneal Soft Tissue Sarcoma (RETRO-WTS)
Official Title
Clinical Phase I/II Trial to Investigate Preoperative Dose-Escalated Intensity-Modulated Radiation Therapy (IMRT) and Intraoperative Radiation Therapy (IORT) in Patients With Retroperitoneal Soft Tissue Sarcoma
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
March 2007 (Actual)
Primary Completion Date
January 2020 (Actual)
Study Completion Date
February 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Heidelberg
Collaborators
German Cancer Research Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Local control rates in patients with retroperitoneal soft tissue sarcoma (RSTS) remain disappointing even after gross total resection, mainly because wide margins are not achievable in the majority of patients. In contrast to extremity sarcoma, postoperative radiation therapy (RT) has shown limited efficacy due to its limitations in achievable dose and coverage. Although Intraoperative Radiation Therapy (IORT) has been introduced in some centers to overcome these dose limitations and resulted in improved outcome, local failure rates are still high even if considerable treatment related toxicity is accepted. As postoperative administration of RT has some general disadvantages, neoadjuvant approaches could offer benefits in terms of dose escalation, target coverage and reduction of toxicity, especially if highly conformal techniques like intensity-modulated radiation therapy (IMRT) are considered.
Therefore the RETROWTS trials has been designed as a prospective, one armed, single center phase I/II study investigating a combination of neoadjuvant dose-escalated IMRT (50-56 Gy) followed by surgery and IORT (10-12 Gy) in patients with at least marginally resectable RSTS. The primary objective is the local control rate after five years. Secondary endpoints are progression-free and overall survival, acute and late toxicity, surgical resectability and patterns of failure. The aim of accrual is 37 patients in the per-protocol population.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Retroperitoneal Soft Tissue Sarcoma
Keywords
retroperitoneal soft tissue sarcoma, IMRT, IORT
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
37 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
A
Arm Type
Experimental
Arm Description
Neoadjuvant Intensity-Modulated Radiation Therapy Followed by Surgery and Intraoperative Radiation Therapy in Resectable Retroperitoneal Soft Tissue Sarcoma
Intervention Type
Radiation
Intervention Name(s)
Neoadjuvant intensity-modulated radiation therapy (IMRT)
Intervention Description
neoadjuvant intensity-modulated radiation therapy, single dose 2.0-2.4 Gy, total dose 50-56 Gy
Intervention Type
Radiation
Intervention Name(s)
intraoperative radiation therapy (IORT)
Intervention Description
during surgery, 10-12 Gy (90% isodose) to the tumor bed or residual disease
Primary Outcome Measure Information:
Title
Local Control Rate
Time Frame
5 year
Secondary Outcome Measure Information:
Title
Progression free survival
Time Frame
up to 5 years from first day of treatment
Title
Overall Survival
Time Frame
up to five years from first day of treatment
Title
Acute toxicity
Description
scored according to CTCAE 3.0
Time Frame
up to 3 months from first day of treatment
Title
Late Toxicity
Description
scored according to CTCAE 3.0 and RTOG criteria
Time Frame
up to 5 years after first day of treatment
Title
Severe acute gastrointestinal toxicity
Description
severe defined as grade >= III, scored according to CTC AE 3.0
Time Frame
up to 3 months from first day of treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
written informed consent
histologically confirmed, primary or locally recurrent soft tissue sarcoma of the retroperitoneal space
judged as at least marginally resectable
absence of distant metastases
tumor size ≥ 5 cm
Exclusion Criteria:
missing written informed consent
missing histological confirmation of soft tissue sarcoma
Desmoid tumor (syn. aggressive fibromatosis)
judged as gross incomplete or not resectable
incomplete staging
presence of distant metastases
prior radiation therapy to the abdominal region
participation in another clinical interventional study
inflammatory bowel disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juergen Debus, M.D., Ph.D.
Organizational Affiliation
University Hospital Heidelberg
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Heidelberg
City
Heidelberg
State/Province
Baden-Württemberg
ZIP/Postal Code
69120
Country
Germany
12. IPD Sharing Statement
Citations:
PubMed Identifier
25163595
Citation
Roeder F, Ulrich A, Habl G, Uhl M, Saleh-Ebrahimi L, Huber PE, Schulz-Ertner D, Nikoghosyan AV, Alldinger I, Krempien R, Mechtersheimer G, Hensley FW, Debus J, Bischof M. Clinical phase I/II trial to investigate preoperative dose-escalated intensity-modulated radiation therapy (IMRT) and intraoperative radiation therapy (IORT) in patients with retroperitoneal soft tissue sarcoma: interim analysis. BMC Cancer. 2014 Aug 27;14:617. doi: 10.1186/1471-2407-14-617.
Results Reference
derived
PubMed Identifier
22788989
Citation
Roeder F, Schulz-Ertner D, Nikoghosyan AV, Huber PE, Edler L, Habl G, Krempien R, Oertel S, Saleh-Ebrahimi L, Hensley FW, Buechler MW, Debus J, Koch M, Weitz J, Bischof M. A clinical phase I/II trial to investigate preoperative dose-escalated intensity-modulated radiation therapy (IMRT) and intraoperative radiation therapy (IORT) in patients with retroperitoneal soft tissue sarcoma. BMC Cancer. 2012 Jul 12;12:287. doi: 10.1186/1471-2407-12-287.
Results Reference
derived
Learn more about this trial
Trial of Neoadjuvant Intensity-Modulated Radiation Therapy Followed by Surgery and Intraoperative Radiation Therapy in Resectable Retroperitoneal Soft Tissue Sarcoma (RETRO-WTS)
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