Preoperative vs Postoperative IMRT for Extremity/Truncal STS

Phase III Study of Preoperative vs Postoperative Intensity Modulated Radiation Therapy For Truncal/Extremity Soft Tissue Sarcoma

This study is designed to determine if preoperative image guided radiation therapy (IGRT) delivered using intensity modulated radiation therapy (IMRT) followed by surgery results in similar short-term wound healing complications as surgery followed by postoperative IGRT in patients with extremity or truncal soft tissue sarcoma. Half of the patients will receive preoperative radiotherapy, half will receive postoperative radiotherapy.

Study Overview

• Status: Active, not recruiting
• Conditions: Adult Soft Tissue Sarcoma
• Intervention / Treatment: Radiation: Preoperative intensity modulated radiation therapy; Radiation: Postoperative intensity modulated radiation therapy

Detailed Description

Perioperative RT in addition to surgery is widely accepted as standard management for soft tissue sarcoma (STS) of the extremity and trunk. However, controversy remains as to whether RT should be delivered preoperatively or postoperatively. While both confer similar rates of local control, preoperative RT leads to a decrease in late tissue morbidities such as fibrosis, limb edema, joint stiffness and fracture as compared to postoperative RT. The reasons for this are likely multifactorial, but are in part related to total dose delivered (50 Gray (GY) preoperatively and 60-66 Gy postoperatively) and, based on a previous National Cancer Institute (Canada) Phase III randomized controlled trial, the much larger volume treated in the postoperative setting compared to that in the preoperative setting. The optimal radiation dose used in the postoperative setting is unknown but has been developed empirically and doses of 60-66 Gy are generally employed.However, investigators in Norway/Sweden and France have found equivalent local control rates for patients with negative surgical margins treated with 50 GY postoperativelyThe main concern with preoperative RT has centered on the risk of an increased rate of delayed wound healing and major wound complications. Although some studies suggest it may be possible to reduce the incidence of acute wound healing complications associated with pre-operative radiation than previously seen in the 2D RT era, this has yet to be tested in the phase III setting. IG-IMRT allows a much higher degree of conformality and accurate delivery of dose to the tumour while sparing surrounding normal tissue. This may allow similar rates of acute wound healing complications for pre- and postoperative RT in the treatment of STS.

• Study Type: Interventional
• Enrollment (Actual): 210
• Phase: Phase 3

Contacts and Locations

Study Locations

• Belgium
  • Brussels, Belgium
    • Cliniques universitaires Saint-Luc
• Canada
  • Ontario
    • Ottawa, Ontario, Canada, K1H 8L6
      • The Ottawa Hospital Cancer Centre
    • Toronto, Ontario, Canada, M5G 2M9
      • Princess Margaret Cancer Centre
    • Toronto, Ontario, Canada, M5G 1X5
      • Mount Sinai Hospital
  • Quebec
    • Montreal, Quebec, Canada, H1T 2M4
      • Hôpital Maisonneuve-Rosemont
• United States
  • Massachusetts
    • Boston, Massachusetts, United States, 02215
      • Dana Farber Cancer Institute
  • Ohio
    • Cleveland, Ohio, United States, 44195
      • Cleveland Clinic Taussig Cancer Institute
  • Oregon
    • Portland, Oregon, United States, 97239-3098
      • Oregon Health & Science University

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 14 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

1. Histologically proven soft tissue sarcoma of the extremity or trunk following review by local reference pathologist.
2. Deemed appropriate for preoperative or postoperative radiotherapy and conservative surgery following patient assessment by a radiation oncologist and surgical oncologist.
3. Lesion is primary or locally recurrent. Patient may have undergone excisional biopsy with positive margins at a referring hospital and are eligible following discussion among the surgical oncologists and radiation oncologists that IMRT is an acceptable treatment for that case.
4. Eastern Cooperative Oncology Group (ECOG) score 0-3
5. Patient is aged 18years or older.
6. Patient is able to provide informed consent
7. Patient is available for treatment and follow-up.

Exclusion Criteria:

1. Benign histology.
2. Prior malignancy within the previous five years or concurrent malignancy with the exception of adequately treated basal cell carcinoma of the skin or carcinoma in-situ of the cervix.
3. Prior radiotherapy to the target site
4. Planned chemotherapy for (neo)adjuvant treatment
5. Conservative surgery to the target site
6. Presence of regional nodal disease or unequivocal distant metastases.
7. Other major medical illness deemed to preclude safe administration of protocol treatment or required follow-up.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Preoperative Radiation Therapy (Arm A); Preoperative intensity modulated radiation therapy followed by surgery	Radiation: Preoperative intensity modulated radiation therapy; 50 Gy delivered in 25 fractions 4-6 weeks prior to surgical excision
Experimental: Postoperative Radiation Therapy (Arm B); Surgery followed by postoperative intensity modulated radiation therapy	Radiation: Postoperative intensity modulated radiation therapy; Surgery followed by 50 Gy delivered in 25 fractions within 6 weeks of surgery for patients with negative margins; for patients with positive margins a boost of 16 Gy in 8 fractions will be added.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Incidence of acute wound healing complications	Secondary operations required for wound treatment (debridement, secondary closure procedures such as rotationplasty, free flaps or skin grafts);; Readmission to hospital for wound care;; Invasive procedures required for wound care (drainage of hematoma, seroma or infected wound collection);; Deep wound packing required at any time (deep packing defined as packing deep to dermis in an area of dehisced wound) to an area of the wound measuring at least 2 cm in length;; Prolonged dressing changes, including packing of the wound for greater than six weeks from wound breakdown;; Repeat surgery for revision of a split thickness skin graft or requirement for wet dressings for longer than four weeks. (It is permissible for a patient to protect a totally epithelialized skin graft with a dry dressing without declaring a major wound complication); Use of vacuum-assisted closure (VAC)	120 days post surgery

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Acute Radiation Toxicity	Acute radiation skin toxicity will be documented according to the Radiotherapy Oncology Group (RTOG) Acute Radiation Morbidity Scoring Criteria.	Once per week from the start of radiotherapy until its completion (5 weeks in total), then 1 week preop for Group 1; 4 weeks post completion of treatment for Group 2
Late Radiation Toxicity- RTOG Late Radiation Morbidity	Late radiation morbidity to skin, subcutaneous tissue, bone and joints will be documented according to the RTOG/EORTC Late Radiation Morbidity Scoring Scheme.	Every 3 months, from 3 months postop for Group 1 and 3 months post RT for Group 2, for 2 years, then 4 monthly for 1 year, then 6 monthly to 5 years.
Late Radiation Toxicity- Common Toxicity Criteria	Late radiation morbidity to skin, subcutaneous tissue, bone and joints will be documented according to the Common Toxicity Criteria v4.0	Every 3 months, from 3 months postop for Group 1 and 3 months post RT for Group 2, for 2 years, then 4 monthly for 1 year, then 6 monthly to 5 years.
Late Radiation Toxicity- Limb Edema	Peripheral limb edema will be documented according to the Late Limb Edema Scoring Criteria.	Every 3 months, from 3 months postop for Group 1 and 3 months post RT for Group 2, for 2 years, then 4 monthly for 1 year, then 6 monthly to 5 years.
Limb Function	Limb function will be documented according to the Musculoskeletal Tumor Society Rating Scale.	Within 14 days of randomization, then at 3 and 6 months, 1, 2, 3 and 5 years postop.
Patient function	Patient function will be documented according to the patient completed Toronto Extremity Salvage Score (TESS)	Within 14 days of randomization, then at 3 and 6 months, 1, 2, 3 and 5 years postop.
Overall Survival	Overall patient survival in months during the study period	Surgery Date until 5 years postoperative or death, whichever occurs first
Local recurrence-free survival	Patient survival without a local recurrence in months during the study period.	Surgery date until 5 years postoperative or local recurrence, whichever occurs first.
Metastasis-free survival	Patient survival without systemic metastases in months during the study period.	Surgery date until 5 years postoperative or systemic recurrence, whichever occurs first.

Collaborators and Investigators

• Sponsor: Mount Sinai Hospital, Canada
• Collaborators: Princess Margaret Hospital, Canada
• Investigators: Principal Investigator: Peter Ferguson, MD, FRCSC, Mount Sinai Hospital; Principal Investigator: Peter Chung, MD, Princess Margaret Cancer Centre

Study record dates

Study Major Dates

• Study Start (Actual): June 1, 2016
• Primary Completion (Estimated): October 1, 2024
• Study Completion (Estimated): May 1, 2029

Study Registration Dates

• First Submitted: September 18, 2015
• First Submitted That Met QC Criteria: September 29, 2015
• First Posted (Estimated): October 1, 2015

Study Record Updates

• Last Update Posted (Actual): February 20, 2024
• Last Update Submitted That Met QC Criteria: February 15, 2024
• Last Verified: February 1, 2024

More Information

Terms related to this study

• Keywords: Soft tissue sarcoma; Postoperative radiotherapy; Extremity; Preoperative radiotherapy
• Additional Relevant MeSH Terms: Neoplasms, Connective and Soft Tissue; Neoplasms by Histologic Type; Neoplasms; Sarcoma
• Other Study ID Numbers: OCREB # 15-070

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO