Study of DPPG2-TSL-DOX Combined With Hyperthermia in Soft Tissue Sarcoma

• Status: Recruiting
• Trial end date: 2024-06-01
• Target enrollment: 0
• Participant gender: All

Summary

This study aims to explore a new therapeutic approach for advanced soft tissue sarcoma (STS) by investigating the safety, tolerability, and maximum tolerable dose (MTD) of DPPG2-TSL-DOX combined with regional hyperthermia (RHT) in patients who have been pre-treated with doxorubicin (DOX).

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Thermosome GmbH
• Treatments: Doxorubicin

Criteria

Inclusion Criteria:

• Age at the time of consent ≥18 years

• Patient has provided written informed consent prior to any study-specific procedure

• Locally advanced (unresectable) or metastatic soft tissue sarcoma (STS) histologically diagnosed by local pathology review for which treatment with doxorubicin (DOX) monotherapy is appropriate, as confirmed by the investigator

• Pretreatment with DOX combination chemotherapy (DOX/ifosfamide, DOX/dacarbazine or other anthracycline combination therapies) provided at least stable disease was achieved. For patients who received DOX in an adjuvant setting, local recurrence free interval of > 6 months is required

• Progressive disease not suitable for surgery after

1. only one further line of chemotherapy (including tyrosine-kinase inhibitor) if the regional hyperthermia (RHT) field targets the clinically relevant tumor manifestation/s (e.g., locally advanced or multifocal intraabdominal STS; diffuse metastatic STS in which RHT of a tumor manifestation [e.g., liver] is considered relevant although other systemic metastases are present that do not endanger the patient, as per the judgment of the investigator), or

2. two or more further lines of chemotherapies (including TKI) for patients with metastatic STS and a tumor manifestation suitable for RHT

• All previous oncological treatments must have been completed ≥3 weeks (21 days) prior to the first dose of study treatment, ensuring a sufficient washout period

• Measurable disease as defined by the Response Evaluation Criteria in Solid Tumors (RECIST 1.1) (Eisenhauer et al. 2009)

• Tumor accessible for RHT

• Left ventricular ejection fraction (LVEF) >50% (within 28 days prior to enrolment)

• Adequate hematologic, organ and coagulation function within 14 days prior to enrolment as assessed by local lab:

1. Absolute neutrophil count (ANC) ≥1.5×10^9/L. Granulocyte-colony stimulating factor (G-CSF) cannot be administered within 2 weeks (14 days) prior to enrolment

2. Platelet count ≥100×10^9/L

3. Hemoglobin ≥9.0 g/dL. No transfusions are allowed within 2 weeks (14 days) prior to enrolment

4. Serum creatinine ≤1.5 times upper limit of normal (ULN)

5. Negative dipstick for proteinuria or if proteinuria ≥2+, then additional 24 h urine collection <1g protein/ 24 h

6. Total bilirubin within ULN (except for patients with Gilbert's syndrome, who must have a total bilirubin <3 mg/dL)

7. Alanine aminotransferase (ALT)/ Aspartate aminotransferase (AST) ≤3.0×ULN; if the liver has tumor involvement, AST and ALT ≤5.0×ULN are acceptable

8. An adequate coagulation function as defined by international normalized ratio (INR) ≤1.5×ULN or prothrombin time ≤1.5×ULN, and partial thromboplastin time ≤1.5×ULN (unless receiving anticoagulant therapy). Patients receiving phenprocoumon are recommended to switch to low molecular weight heparin and should have achieved stable coagulation status prior to the first dose of study treatment

• Tubular excretion rate (TER) by Mercaptoacetyltriglycin-3 (MAG-3)-clearance ≥ TERLoLi (TERLoLi = 70% TERNorm)

• Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2

• If female, must:

1. Be not of child-bearing potential due to surgical sterilization (at least 6 weeks following surgical bilateral oophorectomy with or without hysterectomy or tubal ligation) confirmed by medical history or menopause

2. Be a post-menopausal woman, defined as a woman meeting either of the following criteria:

i. spontaneous amenorrhea for at least 12 months, not induced by a medical condition such as anorexia nervosa and not taking medications during the amenorrhea that induced the amenorrhea (for example, oral contraceptives, hormones, gonadotropin-releasing hormone, antiestrogens, selective estrogen receptor modulators [SERMs], or chemotherapy) ii. spontaneous amenorrhea for 6 to 12 months and a follicle-stimulating hormone level >40 mIU/mL

• Women of childbearing potential (WOCBP) and men able to father a child must be ready and able to use two medically acceptable methods of birth control per ICH M3 (R2) that result in a low failure rate of less than 1 percentage per year when used consistently and correctly beginning at screening, during trial participation, and until 6 months after last dose of study treatment. Also, partner of male participants, who is of childbearing potential must use a highly effective method of contraception during the same duration.

• At least 3 months' life expectancy in the investigator's assessment

Exclusion Criteria:

• Progressive disease under previous treatment with anthracyclines

• Patients already enrolled in any clinical study involving an investigational product or medical device or have participated within the past 30 days in a clinical trial involving an investigational product or medical device

• History of another primary malignancy, with the exception of:

1. curatively treated non-melanomatous skin cancer

2. curatively treated cervical carcinoma in situ

3. non-metastatic prostate cancer, or

4. other primary non-hematologic malignancies that had been treated with curative intent, no known active disease, and no treatment administered during the last 3 years prior to enrolment that the investigator agrees will not affect the interpretation of study results or would be unsuitable for participation in the study

• Active fungal, bacterial and/or known viral infection including human immunodeficiency virus or viral (A, B, or C) hepatitis

• Resting heart rate of >100 bpm

• Uncontrolled intercurrent illness including, but not limited to, an ongoing/active infection - - Have a serious cardiac condition, such as:

1. unstable angina pectoris

2. angioplasty, cardiac stenting, or myocardial infarction within 6 months of enrolment

3. valvulopathy that is severe, moderate, or deemed clinically significant

4. arrhythmias that are symptomatic or require treatment

• Have a QTcF interval of >450 msec for males and >470 msec for females on screening electrocardiogram (ECG) utilizing Fridericia's correction

• Psychiatric illness or social situation that would limit compliance with study requirements.

• Any planned or required major surgery during the course of the study

• Pregnant or breastfeeding female

• Individuals who are institutionalized on a judicial or regulatory order