Feasibility of Total Neoadjuvant Treatment With HYPErthermia in Patients With High-risk Extremity and Trunk Soft Tissue Sarcoma (TNT-HYPE)
Sponsor: Swiss Cancer Institute · NCT06835049 on ClinicalTrials.gov ↗
Conditions studied
What it tests
- Doxorubicindrug
- Ifosfamidedrug
- Dacarbazinedrug
- Hyperthermiaother
- Radiotherapyradiation
- Surgeryprocedure
Where it's running8 sites
8 international sites
- Recruiting now
Kantonsspital Aarau
Aarau, Switzerland 5001
- Oliver Riesterer, Prof.(contact)+41 62 838 42 49[email protected]
- Oliver Riesterer, Prof.(principal investigator)
- Recruiting now
Universitaetsspital Basel
Basel, Switzerland CH-4031
- Fatime Krasniqi, MD(contact)+41 61 265 50 59[email protected]
- Fatime Krasniqi, MD(principal investigator)
- Recruiting now
EOC - Istituto Oncologico della Svizzera Italiana
Bellinzona, Switzerland 6500
- Thomas Zilli, Prof(contact)+41 91 811 86 75[email protected]
- Thomas Zilli, Prof(principal investigator)
- Recruiting now
Inselspital Bern - Universitätsklinik für Radioonkologie
Bern, Switzerland 3010
- Emanuel Stutz, MD(contact)+41 31 632 26 32[email protected]
- Emanuel Stutz, MD(principal investigator)
- Recruiting now
CHUV - Swiss Cancer Center Lausanne
Lausanne, Switzerland 1011
- Antonia Digklia, MD(contact)+41 21 314 79 28[email protected]
- Antonia Digklia, MD(principal investigator)
- Recruiting now
hoch Health Ostschweiz - Kantonsspital St. Gallen
Sankt Gallen, Switzerland 9007
- Christina Appenzeller, MD(contact)+41 71 494 29 22[email protected]
- Christina Appenzeller, MD(principal investigator)
- Recruiting now
Kantonsspital Winterthur
Winterthur, Switzerland 8401
- Ralph Zachariah, MD(contact)+41 52 266 30 65[email protected]
- Ralph Zachariah, MD(principal investigator)
- Recruiting now
Universitätsspital Zürich
Zurich, Switzerland 8091
- Lorenz Bankel, MD(contact)+41 44 255 22 14[email protected]
- Lorenz Bankel, MD(principal investigator)
See the official eligibility language
Shown exactly as written on ClinicalTrials.gov. Your oncologist is the right person to judge whether it fits your situation.
Main Inclusion Criteria: * 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. Main Exclusion Criteria: * Metastatic disease. * Previous Whoops resection. * Ex-ulcerating tumors or tumors infiltrating the skin. * Other invasive malignancy within 5 years, with the exception of adequately treated non melanoma skin cancer, localized cervical cancer, localized and Gleason ≤ 6 prostate cancer. * Any previous radiotherapy (RT) or systemic therapy for the present tumor. * Previous treatment with maximum cumulative doses (450 mg/m² doxorubicin or equivalent 900 mg/m² epirubicin) of doxorubicin, daunorubicin, epirubicin, idarubicin, and/or other anthracyclines and anthracenediones. * Concomitant or recent (within 30 days of registration) treatment with any other experimental drug. * Concomitant use of other anti-cancer drugs or RT. * No metal implants in the region of tumor or cardiac implant electronic devices (CIEDs). * Severe or uncontrolled cardiovascular disease (congestive heart failure NYHA III or IV), unstable angina pectoris, history of myocardial infarction within the last 12 months, serious arrhythmias requiring medication (with exception of atrial fibrillation or paroxysmal supraventricular tachycardia), significant QT-prolongation, uncontrolled hypertension. * Active and uncontrolled infections, in particular urinary tract infections. * Inflammation of the urinary bladder (interstitial cystitis). * History of cerebrovascular accident or intracranial hemorrhage within 6 months prior to registration. * Vaccination with live vaccines within 30 days prior to registration. * Known hypersensitivity to trial drug(s) or to any component of the trial drug(s).
Updated 2025-12-30 on ClinicalTrials.gov. Always confirm current details with the study team or your oncologist.