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Preoperative vs Postoperative IMRT for Extremity/Truncal STS

Phase 3
Active, not recruiting
Conditions
Adult Soft Tissue Sarcoma
Interventions
Radiation: Preoperative intensity modulated radiation therapy
Radiation: Postoperative intensity modulated radiation therapy
Registration Number
NCT02565498
Lead Sponsor
Mount Sinai Hospital, Canada
Brief Summary

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.

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.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
210
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 & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Preoperative Radiation Therapy (Arm A)Preoperative intensity modulated radiation therapyPreoperative intensity modulated radiation therapy followed by surgery
Postoperative Radiation Therapy (Arm B)Postoperative intensity modulated radiation therapySurgery followed by postoperative intensity modulated radiation therapy
Primary Outcome Measures
NameTimeMethod
Incidence of acute wound healing complications120 days post surgery

* 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)

Secondary Outcome Measures
NameTimeMethod
Acute Radiation ToxicityOnce 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

Acute radiation skin toxicity will be documented according to the Radiotherapy Oncology Group (RTOG) Acute Radiation Morbidity Scoring Criteria.

Late Radiation Toxicity- RTOG Late Radiation MorbidityEvery 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 morbidity to skin, subcutaneous tissue, bone and joints will be documented according to the RTOG/EORTC Late Radiation Morbidity Scoring Scheme.

Late Radiation Toxicity- Common Toxicity CriteriaEvery 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 morbidity to skin, subcutaneous tissue, bone and joints will be documented according to the Common Toxicity Criteria v4.0

Late Radiation Toxicity- Limb EdemaEvery 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.

Peripheral limb edema will be documented according to the Late Limb Edema Scoring Criteria.

Patient functionWithin 14 days of randomization, then at 3 and 6 months, 1, 2, 3 and 5 years postop.

Patient function will be documented according to the patient completed Toronto Extremity Salvage Score (TESS)

Limb FunctionWithin 14 days of randomization, then at 3 and 6 months, 1, 2, 3 and 5 years postop.

Limb function will be documented according to the Musculoskeletal Tumor Society Rating Scale.

Local recurrence-free survivalSurgery date until 5 years postoperative or local recurrence, whichever occurs first.

Patient survival without a local recurrence in months during the study period.

Overall SurvivalSurgery Date until 5 years postoperative or death, whichever occurs first

Overall patient survival in months during the study period

Metastasis-free survivalSurgery date until 5 years postoperative or systemic recurrence, whichever occurs first.

Patient survival without systemic metastases in months during the study period.

Trial Locations

Locations (8)

Cleveland Clinic Taussig Cancer Institute

🇺🇸

Cleveland, Ohio, United States

Dana Farber Cancer Institute

🇺🇸

Boston, Massachusetts, United States

Oregon Health & Science University

🇺🇸

Portland, Oregon, United States

Cliniques Universitaires Saint-Luc

🇧🇪

Brussels, Belgium

The Ottawa Hospital Cancer Centre

🇨🇦

Ottawa, Ontario, Canada

Mount Sinai Hospital

🇨🇦

Toronto, Ontario, Canada

Princess Margaret Cancer Centre

🇨🇦

Toronto, Ontario, Canada

Hopital Maisonneuve-Rosemont

🇨🇦

Montreal, Quebec, Canada

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