A Phase Ib Trial of Eribulin in Combination with Irinotecan and Temozolamide in Children with Relapsed or Refractory Solid Tumors

Trial Title: A Phase Ib Trial of Eribulin in Combination with Irinotecan and Temozolamide in Children with Relapsed or Refractory Solid Tumors

NCT ID: NCT06006273

Condition: Refractory Solid Tumors

Conditions: Official terms:
Neoplasms
Irinotecan
Temozolomide

Study type: Interventional

Study phase: Phase 1/Phase 2

Overall status: Recruiting

Study design:

Allocation: Randomized

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Eribulin
Description: Given by vein (IV)
Arm group label: Arm A: Dose expansion-Ewings sarcoma
Arm group label: Arm B: Dose expansion -Rhabdomyosarcoma
Arm group label: Arm C: Dose expansion- other solid tumor histologies
Arm group label: Arm D: Dose finding levels 0,-1 and -2

Intervention type: Drug
Intervention name: Irinotecan
Description: Given by vein (IV)
Arm group label: Arm A: Dose expansion-Ewings sarcoma
Arm group label: Arm B: Dose expansion -Rhabdomyosarcoma
Arm group label: Arm C: Dose expansion- other solid tumor histologies
Arm group label: Arm D: Dose finding levels 0,-1 and -2

Intervention type: Drug
Intervention name: Temozolomide
Description: Given by PO
Arm group label: Arm A: Dose expansion-Ewings sarcoma
Arm group label: Arm B: Dose expansion -Rhabdomyosarcoma
Arm group label: Arm C: Dose expansion- other solid tumor histologies
Arm group label: Arm D: Dose finding levels 0,-1 and -2

Summary: To find the recommended dose of eribulin that can be given in combination with irinotecan and temozolomide to treat relapsed and/or refractory solid tumors.

Detailed description: Primary Objectives: - To determine the maximum tolerated dose (MTD)/ recommended phase 2 dose (RP2D) of eribulin in combination with fixed doses of irinotecan and temozolomide. - To determine the safety and tolerance of Eribulin when given in conjunction with Irinotecan and Temozolamide (IT) in children with refractory and relapsed (R/R) solid tumors. Secondary Objectives: --To observe and record disease response (anti-tumor activity). Although the clinical benefit of Eribulin when given together with Irinotecan and Temozolamide has not yet been established, the intent of offering this treatment is to provide a possible therapeutic benefit, and thus the patient will be carefully monitored for tumor response and symptom relief. Outcomes for disease response include Best Overall Response (BOR), Duration of Response (DOR), and Progression-Free Survival (PFS).

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Age: Patients must be > 1 year of age and ≤ 25 years of age at time of initiation of protocol therapy. - Diagnosis: Patients have a histologically or radiographically confirmed relapsed or refractory solid tumor. - Disease Status: Patients must have evaluable disease. - Patients may have CNS metastases at study entry, if they are previously treated or stable (defined by not requiring initation or increased steroids for 7 days). - Performance Level: Karnofsky ≥ 50% for patients >16 years old, and Lansky ≥ 50 for patients 1-16 years old. (Appendix I) - Prior Therapy: Patients may have received prior therapy including single-agent irinotecan or temozolomide. Patients may not have previously been treated with combination therapy of irinotecan and temozolomide. - Patients must be fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study. 1. Hematopoietic growth factor: At least 7 days must have elapsed since the last administration of filgrastim, or 14 days since administration of pegfilgrastim. 2. XRT: At least 7 days since the last dose of local palliative radiation therapy. Greater than 6 months must have elapsed since the last day of treatment if given total body irradiation, craniospinal irradiation. 3. Autologous or Allogenic Stem Cell Transplant: Complete resolution of graft versus host disease and no current need for immunosuppressive medication. Greater than 3 months must have elapsed since engraftment and no longer requiring transfusion of platelets or injection of colony stimulating factors. - Organ Function Requirements - Bone Marrow Function: 1. Peripheral absolute neutrophil count (ANC) ≥ 750/µL 2. Platelet count ≥ 75,000/µL (no platelet transfusion within 7 days prior to obtaining laboratory result) - Adequate Renal Function: a. Creatinine clearance or glomerular filtration rate ≥ 70ml/min/1.73m2 (calculated or measured as appropriate for age and level of concern by treating MD) - Adequate Liver Function: 1. Total bilirubin ≤ 1.5x upper limit of normal (ULN) for age 2. SGPT (ALT) ≤ 3 x ULN 3. Serum albumin ≥ 2gm/dL Due to the risk of hepatic injury, including fatal hepatic failure, temozolomide should not be administered if total bilirubin is >2.0 mg/dl or SGPT(ALT)> 3 x ULN. Informed Consent: All patients ≥ 18 years of age must sign a written informed consent. For patients < 18 years old, the patient's parents or legal guardians must sign a written informed consent, unless the patient is an emancipated minor. Childhood Assent, when age appropriate as per institutional guidelines, should be signed by the participating patient. Consent may be obtained virtually, as per institutional guidelines. Exclusion Criteria: - Significant organ dysfunction, not meeting inclusion criteria. - Pediatric subjects who are considered wards of some entity - Pregnancy or Breast-Feeding - Pregnant or breast-feeding woman will not be entered on this study due to risks of fetal and teratogenic adverse events as seen in animal/human studies. - Concomitant Medications: - Growth factor: Growth factors that support platelet or white cell number of function must not have been administered within the past 7 days. - Investigational Drugs: Patients who are currently receiving another investigational drug. (Please refer to Prior Therapy, section 2.1.5) - Anti-cancer Agents: Patients who are currently receiving other anti-cancer agents. (Please refer to Prior Therapy, section 2.1.5.1) - Medication Allergy: 1. Allergy or intolerance to agents on this protocol: irinotecan, temozolomide, or eribuin 2. Allergy to cephalosporins, without a reasonably available antibiotic alternative - Infection: Patients who have uncontrolled infection, positive blood cultures within the past 48 hours, or receiving treatment for Clostridium difficile infection.

Gender: All

Minimum age: 1 Year

Maximum age: 25 Years

Healthy volunteers: No

Locations:

Facility:
Name: M D Anderson Cancer Center

Address:
City: Houston
Zip: 77030
Country: United States

Status: Recruiting

Contact:
Last name: Fiorela Hernandez Tejada, MD

Phone: (832) 306-9802
Email: fnhernandez@mdanderson.org

Contact backup:
Last name: Fiorela Hernandez Tejada, MD

Start date: August 16, 2023

Completion date: December 31, 2028

Lead sponsor:
Agency: M.D. Anderson Cancer Center
Agency class: Other

Source: M.D. Anderson Cancer Center

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

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06006273
http://www.mdanderson.org