Feasibility of Total Neoadjuvant Treatment With HYPErthermia in Patients With High-risk Extremity and Trunk Soft Tissue Sarcoma (TNT-HYPE). A Multicenter, Single Arm, Open Label, Phase II Trial

Status: Recruiting
Location: See all (8) locations...
Intervention Type: Drug, Other, Procedure, Radiation
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Soft tissue sarcomas (STSs) are rare cancers with a 5-year survival rate of 60%, and there is no standard treatment for high-risk extremity and trunk STSs (eSTS). A phase III trial suggests that adding moderate regional hyperthermia (HT) to anthracycline-based chemotherapy, followed by surgery and radiotherapy (RT), can improve 10-year overall survival by 10%. This trial aims to optimize treatment by combining the most effective regimens from chemotherapy, HT, RT, and surgery, and will evaluate the feasibility of this new total neoadjuvant treatment (TNT) approach.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Histologically confirmed primary high-risk Soft tissue sarcoma (STS) of extremity or trunk.

• High-risk according to the prognostic Sarculator tool: 10-year OS probability \< 60%5.

• Resectable tumor: resectability is based on pre-operative imaging and has to be defined by the local treating sarcoma team. A patient is not considered resectable when the expectation is that only a R2 resection is feasible.

• Measurable disease per RECIST v1.1.

• Diagnostic biopsy is available for the central pathology review.

• Candidate for chemotherapy regimen according to protocol.

• Candidate for loco-regional HT.

• Adequate bone marrow function, hepatic function, renal function, cardiac function and coagulation function.

Locations
Other Locations
Switzerland
Kantonsspital Aarau
RECRUITING
Aarau
Universitaetsspital Basel
RECRUITING
Basel
EOC - Istituto Oncologico della Svizzera Italiana
RECRUITING
Bellinzona
Inselspital Bern - Universitätsklinik für Radioonkologie
RECRUITING
Bern
CHUV - Swiss Cancer Center Lausanne
RECRUITING
Lausanne
hoch Health Ostschweiz - Kantonsspital St. Gallen
RECRUITING
Sankt Gallen
Kantonsspital Winterthur
RECRUITING
Winterthur
Universitätsspital Zürich
RECRUITING
Zurich
Contact Information
Primary
Gwendoline Wicki
trials@sakk.ch
+41 31 389 91 91
Time Frame
Start Date: 2025-11-15
Estimated Completion Date: 2031-03-31
Participants
Target number of participants: 24
Treatments
Experimental: Neoadjuvant Treatment
Trial treatment consists of 3 neoadjuvant cycles of doxorubicin with either ifosfamide or dacarbazine (the latter only in case of leiomyosarcoma) combined with hyperthermia (HT), followed by radiotherapy (RT) and surgery. Each chemotherapy cycle will last 3 weeks. Trial treatment will last approximately 20 weeks. After surgery, a follow-up period of 36 months per patient is foreseen.
Related Therapeutic Areas
Sponsors
Leads: Swiss Cancer Institute

This content was sourced from clinicaltrials.gov