Sodium Thiosulfate Otoprotection During Salvage Cisplatin Therapy

Trial Title: Sodium Thiosulfate Otoprotection During Salvage Cisplatin Therapy

NCT ID: NCT05756660

Condition: Ototoxicity, Drug-Induced

Conditions: Official terms:
Hepatoblastoma
Ototoxicity
Sodium thiosulfate
Cisplatin
Vorinostat

Conditions: Keywords:
Cisplatin
Sodium Thiosulfate
Relapsed/Refractory Hepatoblastoma
PedMark
Embryonal Tumor

Study type: Interventional

Study phase: Early Phase 1

Overall status: Recruiting

Study design:

Allocation: Non-Randomized

Intervention model: Parallel Assignment

Intervention model description: Three strata are identified for this study: Stratum 1: Cisplatin sensitive/no progression on cisplatin (when given at first diagnosis): Regimen Cisplatin/STS (CS) Stratum 2A: Cisplatin resistant or progressed on cisplatin after initial response (when given at first diagnosis): Regimen Cisplatin/STS/SAHA (CSS) Stratum 2B: Wilms tumor, Germ Cell tumor, Neuroblastoma: Regimen CSS Within each of the 3 eligible strata, patients will be enrolled and directly assigned to their respective protocol therapy, yielding 3 independent single-arm cohorts. Patients will receive protocol therapy for up to 6 3-week cycles before moving to follow-up.

Primary purpose: Supportive Care

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Sodium Thiosulfate
Description: This goal of this study is to evaluate the efficacy of the proposed regimens in patients with relapsed/refractory platinum pre-treated patients with Hepatoblastoma, Wilms tumor, Germ Cell Tumor (GCT), and Neuroblastoma. The patients' initial cisplatin response (hepatoblastoma) and diagnosis will determine their treatment regimen on this study.
Arm group label: Stratum 1- Regimen CS
Arm group label: Stratum 2A- Regimen CSS
Arm group label: Stratum 2B- Regimen CSS

Other name: Cisplatin

Other name: Vorinostat/ SAHA

Summary: This study will attempt to demonstrate the efficacy of Sodium Thiosulfate (STS) in preventing hearing loss in patients re-treated with cisplatin-based therapy according to regimens Cisplatin and STS (regimen CS) and Cisplatin, STS and Vorinostat/SAHA (regimen CSS).

Detailed description: This trial will assess the effect of STS in preventing subsequent hearing loss when patients are re-challenged with cisplatin therapy at relapse/progression, as well as the efficacy of cisplatin/STS or cisplatin/STS/SAHA for patients with relapsed hepatoblastoma, Wilms, Germ Cell Tumor (GCT) and Neuroblastoma stratified by initial cisplatin sensitivity. Important pharmacokinetic measurements focused on cisplatin and STS in children, with varying degrees of renal function, will be assessed. Such pharmacokinetic data will fill a current gap in our clinical knowledge base and enable safer use of such agents for all children with such cancers, regardless of kidney function, in the future.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Patients must be > 1 month and ≤ 39 years old at study enrollment - Histologically proven, at time of diagnosis or relapse: 1. Stratum 1: Arm CS (Cisplatin/STS): Previously chemosensitive to cisplatin defined as an AFP drop of 1 log (90%) and/or an objective tumor response of 30% or greater on imaging while receiving cisplatin. 2. Stratum 2A: Cisplatin/STS/SAHA (CSS): Previously chemosensitive but with noted subsequent progression on cisplatin or initially chemoresistant to cisplatin (all other hepatoblastoma patients). Resistance to cisplatin is defined as rising alpha-fetoprotein (AFP) x 2 consecutive measurements or imaging progression including growth of known lesions or new lesions while patient is receiving a cycle of chemotherapy containing cisplatin or relapse noted within 3 months of last cisplatin administration. 3. Stratum 2B: CSS: Relapsed/refractory Wilms tumor, Germ Cell Tumor, or Neuroblastoma - Patients must have a life expectancy of ≥ 8 weeks. - Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study: 1. Myelosuppressive chemotherapy: Must not have received within 2 weeks of entry onto this study. Previous SAHA administration is permitted. Tacrolimus and Sirolimus with levels <= 10 ng/ml are not considered myelosuppressive. 2. Immunotherapy: Must not have received within 2 weeks of entry onto this study. 3. Radiation therapy (RT): greater than or equal to 2 weeks for local palliative RT (small port); greater than or equal to 6 months must have elapsed if prior craniospinal RT or if greater than or equal to 50% radiation of pelvis - Patients may not be enrolled on another clinical trial or receiving any other investigational therapies (within 2 weeks prior to study enrollment). - Organ Function Requirements 1. Adequate Bone Marrow Function Defined as: 1. Peripheral absolute neutrophil count (ANC) greater than or equal to 750/uL 2. Platelet count greater than or equal to 75,000/uL (transfusion independent defined as no platelet transfusions within 7 days) 3. Hemoglobin greater than or equal to 8.0 g/dL (may receive red blood cell transfusions) 2. Adequate Liver Function Defined As: 1. Total OR direct bilirubin less than or equal to 1.5 x upper limit of normal (ULN) for age, and 2. Aspartate aminotransferase (AST) or Alanine transaminase (ALT) < 10x ULN 3. Adequate Renal Function Defined As: 1. Creatinine clearance or radioisotope glomerular filtration rate (GFR) > 30 mL/min/1.73 m2 - Baseline Audiology Requirements: 1. Subjects must have a successful audiology examination prior to enrollment. Patients may have Boston grade III or IV hearing loss and still be eligible to enroll as long as they did not receive 3 or more cycles of cisplatin during upfront therapy WITH sodium thiosulfate. There is no specific baseline hearing level/grade requirement beyond that to be eligible, but the baseline level of hearing must be clearly established and recorded Exclusion Criteria: - Patients with any uncontrolled, intercurrent illness including, but not limited to, uncontrolled infection - Patients with symptomatic congestive heart failure (defined as Grade 2 or higher heart failure per CTCAE version 5.0) - Patients with Renal Tubular Acidosis (RTA) as evidenced by serum bicarbonate < 16 mmol/L and serum phosphate ≤ 2 mg/dL (or < 0.8 mmol/L) without supplementation. Patients requiring electrolyte supplementation for RTA will be permitted if bicarbonate ≥16 mmol/L and phosphate > 2mg/dL after at least 7 days of stable supplementation regimen - Pregnancy and Breastfeeding: 1. Female patients who are pregnant or breast-feeding will not be entered in the study. A negative pregnancy test within 72 hours of starting therapy is required for female patients of childbearing potential 2. Lactating females who plan to breastfeed their infants. 3. Sexually active patients of reproductive potential must agree to use an effective contraceptive method for the duration of their study participation - Patients on tacrolimus and/or sirolimus with levels of either targeted > 10 ng/mL - Known allergy to any component of CS or CSS therapy, as indicated

Gender: All

Minimum age: 1 Month

Maximum age: 39 Years

Healthy volunteers: No

Locations:

Facility:
Name: Cincinnati Children's Hospital Medical Center

Address:
City: Cincinnati
Zip: 45229
Country: United States

Status: Recruiting

Contact:
Last name: Site Public Contact

Phone: 513-636-2799
Email: cancer@cchmc.org

Investigator:
Last name: James Geller, MD
Email: Principal Investigator

Start date: March 1, 2023

Completion date: January 2027

Lead sponsor:
Agency: Children's Hospital Medical Center, Cincinnati
Agency class: Other

Source: Children's Hospital Medical Center, Cincinnati

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05756660
http://www.cincinnatichildrens.org/service/c/cancer-blood