Safety Study of Whole Body Hyperthermia for Advanced Cancer

Inclusion criteria: 1. Patients between 18- and 75-years of age at time of signing the informed consent 2. Patients with advanced solid cancer (for cohort A1, A2 only) or metastatic pancreatic adenocarcinoma confirmed by histology (for cohort B/C/D only) 3. Patients previously treated or under treatment with standard of care treatment (cohort B/C/D only) or patients without treatment options 4. WHO performance status ≤ 1(see appendix V) 5. Maximum waist circumference ≤ 150 cm 6. Weight ≤ 100 kg 7. Height ≤ 1,90 m 8. Adequate liver structure (confirmed by CT scan) allowing the placement of the liver sensor 9. No (prostate) pathology that would interfere with the placement of the bladder catheter 10. Adequate bone marrow function defined as 1. white blood cell count ≥ 2000/µl 2. neutrophils ≥ 1500 cells/μL 3. platelets ≥ 100 x 109/L 4. hemoglobin ≥ 10 g/dl documented within 1 week prior to first treatment 11. Adequate coagulation defined as 1. PT (%) ≥ 70% 2. aPTT ≤ ULN 3. Von Willebrand Factor Antigen ≥ LLN 4. Von Willebrand Factor Activity ≥ LLN 5. PFA COL/EPI CT ≤ 1.15 ULN 6. PFA COL/ADP CT ≤ 1.15 ULN 12. Adequate liver function defined as 1. Transaminases (AST, ALT) ≤ 2.5 x ULN or ≤ 5.0 in presence of liver metastasis 2. bilirubin ≤ 2 x ULN documented 13. Adequate renal function defined as 1. serum creatinine ≤ 1.6 mg/dL (male); ≤ 1.3 mg/dL (female); 2. albumin ≥ 30g/L 3. calculated eGFR ≥ 60 mL/min (CKD-EPI equation) documented within 1 week prior to randomization 14. No blood donation 3 months prior to the WBHT treatment 15. No participation in other clinical trial 4 weeks prior to the WBHT treatment 16. No biological therapy 4 weeks prior to the WBHT treatment or during WBHT treatment 17. No surgery 4 weeks prior to the WBHT treatment 18. No radiotherapy 3 weeks prior to the WBHT treatment or during WBHT treatment 19. No chemotherapy 1 week prior to the WBHT treatment (for cohort A/B/C/D) or during WBHT treatment (for Cohort A1/A2) 20. No anti-platelet aggregation medication intake from 5 days prior to the first WBHT treatment until 5 days after the last treatment 21. No anticoagulant medication intake between screening and last follow-up visit. However, if deemed necessary by the investigator, the patient may receive prophylactic Low Molecular Weight Heparin on the day prior to the first WBHT treatment until 10 days after the last WBHT treatment 22. No transdermal patches during participation in the study 23. No piercings (internally or externally)during WBHT treatment 24. Life expectancy of at least 18 weeks 25. Effective contraception for both male and female patients if applicable. Women of childbearing potential must have negative blood pregnancy test at screening visit. 26. Written informed consent must be given according to good clinical practice and national/local regulations. Exclusion criteria: 1. Pregnant or breastfeeding women (based on HCG levels) 2. Presence of brain metastasis (known or suspected) 3. Other malignant diseases in the medical history during the last 5 years (exceptions: carcinoma in situ of the cervix or adequately treated basal cell carcinoma of the skin) 4. Serious medical risk factors involving any of the major organ systems, including high cardiovascular risk, coronary stenting or myocardial infarction in the last year 5. Clinically significant pulmonary disease which might interfere with mechanical ventilation 6. History of autonomic dysfunction (due to the influence on skin blood flow) 7. History of malignant hyperthermia or a positive diagnostic test (Caffeine-Halothane Contracture test) in case of family history of malignant hyperthermia. 8. History of untreated endocrine pathology (e.g. diabetes type II, hyper- or hypothyroidism). 9. Primary diabetes type I (due to vascular complications) 10. Known allergies to drugs that will be used during the trial (e.g. anesthetic, analgesic, (chemotherapy used in cohort B/C/D)) 11. Active infections not controlled by medication 12. Severe, non-healing wounds, ulcers or bone fractures 13. Organ allografts requiring immunosuppressive therapy 14. (History of) clinically significant (investigator decision) psychiatric disorder and/or psychosocial disorder that may interfere with adequate compliance to the protocol or signature of the informed consent 15. Other clinically significant disease which could impair the patient's ability to participate in the study according to the investigator's opinion 16. Participation in another clinical trial during this trial