Lurbinectedin for the Treatment of Patients with Relapsed FET-Fused Tumors
This phase I/II tests the safety, side effects, effectiveness and best dose of lurbinectedin for the treatment of patients with FET-fused tumors that has come back after a period of improvement (relapsed). Chemotherapy drugs, such as lurbinectedin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading.
Inclusion Criteria
- Age ≥ 10 years
- PHASE I: Histological confirmed diagnosis of recurrent or relapsed solid tumor failing primary therapy. Patients must have a known FET fusion (fusion that contains EWSR1, FUS, or TAF15) as documented by next generation sequencing, polymerase chain reaction (PCR) or fluorescence in situ hybridization (FISH). Patients with a histological diagnosis of Ewing sarcoma with EWS-FLI1 are eligible for dose escalation but not for the exploratory cohort. Please note patients with Ewing sarcoma and alternative FET-ETS fusions (including but not limited to EWS-ERG, EWS-ETV1, EWS-ETV4, EWS-FEV, FUS-ERG, FUS-FEV) are eligible for the exploratory cohort
- PHASE II: Histologically confirmed diagnosis of recurrent or relapsed Ewing sarcoma failing primary therapy with confirmation of EWS-FLI1 fusion and breakpoint by next generation sequencing or PCR or EWSR1 rearrangement confirmed by FISH and available tissue for central confirmation of EWS-FLI1 fusion and breakpoint
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 (age >16 years) or Lansky of at least 60 (age <16 years)
- Disease status (baseline imaging must be performed within 28 days of day 1 of study treatment): * Phase 1: At least one site of measurable disease on CT or MRI as defined by RECIST 1.1 OR evaluable disease with at least one site of disease that has not been previously radiated * Phase 2: At least one site of measurable disease on CT or MRI as defined by RECIST 1.1
- Alanine aminotransferase (ALT) =< 2.5X upper limit of normal (ULN) * For the purposes of this study the ULN for ALT is 45 U/L
- Aspartate aminotransferase (AST) =< 2.5 X ULN * For the purposes of this study the ULN for AST is 50 U/L
- Total bilirubin ≤ 1.5 X institutional ULN with the exception of patients with Gilbert’s syndrome who must have bilirubin < 3 X institutional ULN
- Creatinine Calculated creatinine clearance (by the Schwartz equation for patients <18 years of age and Cockroft-Gault formula for patients >18 years of age) or radionuclide glomerular filtration rate (GFR) ≥ 50 mL/min /m^2 or a serum creatinine less than or equal to the age/gender valued from the Schwartz formula for estimating GFR utilizing child length and stature data published by the Center for Disease Control (CDC)
- Absolute neutrophil count ≥ 1,000/µL (>one week since last dose of short acting medications (e.g. filgrastim) and > two weeks since last dose of long acting medications (e.g. peg-filgrastim) * Patients with a history of bone marrow involvement are required to have bilateral bone marrow aspirates and biopsies at baseline. Subjects with bone marrow disease are eligible as long as they meet the hematologic requirements above and are not known to be refractory to red cell or platelet transfusions
- Platelets (PLTs) ≥ 100,000/ µL (without platelet transfusion within previous 7 days of screening laboratories) * Patients with a history of bone marrow involvement are required to have bilateral bone marrow aspirates and biopsies at baseline. Subjects with bone marrow disease are eligible as long as they meet the hematologic requirements above and are not known to be refractory to red cell or platelet transfusions
- Creatine phosphokinase ≤ 2.5 x institutional ULN
- Left ventricular ejection fraction or shortening fraction per institutional norm. >= institutional lower limit of normal (LLN)
- Written, voluntary informed consent
- Fertile males and females of childbearing potential must agree to use an effective method of birth control from screening, through day 1 of study and for 6 months after last study drug administration for females and 4 months for males. Women of childbearing potential must have a negative pregnancy test during screening procedures. Effective methods of birth control include: double barrier method (condom, diaphragm), abstinence, an intrauterine device (IUD), levonorgestrol implants, medroxyprogesterone acetate injections, or oral contraception. For those subjects whose preferred and usual lifestyle employs abstinence, refraining from heterosexual intercourse must be practiced during the entire active phase of the trial
- Patients ≥18 years must be willing to undergo tumor biopsy at study entry. Patients with Ewing sarcoma or desmoplastic small round cell tumor (DSRCT) must be willing to undergo biopsy post-treatment. If biopsy is contraindicated, enrollment must be approved by study PI and archival tissue must be available
- Time elapsed from previous therapy: * Must be >= 3 weeks for systemic myelosuppressive therapy * >= 2 weeks for local radiation therapy (small field), > 150 days after total body irradiation (TBI), craniospinal radiation (XRT) or radiation to >50% of the pelvis * >= 2 weeks for major surgery * >= 2 weeks for monoclonal antibodies and oral kinase inhibitors * >= 6 weeks for autologous stem cell transplant. 6 months for allogeneic stem cell transplant * >= 6 weeks for any type of cellular therapy
- Patients must be recovered to baseline or grade ≤1from the acute adverse effects of prior treatments, with the exception of alopecia and decreased deep tendon reflexes
Exclusion Criteria
- Prior therapy with trabectedin or lurbinectedin
- Subjects with known brain metastases
- Subjects with a known bleeding diathesis
- Subjects who are pregnant or breastfeeding
- Concurrent therapy: * Patients who are currently receiving an investigational drug or another anticancer agent * Patients receiving over the counter or herbal supplement with significant potential hepatotoxicity in the opinion of the investigator * Patients receiving a medically necessary strong or moderate CYP3A4 inhibitor or inducer within 14 days prior to the first dose of study drug
- Clinically significant, unrelated illness or uncontrolled infection which would, in the opinion of the treating physician, compromise the patient’s ability to tolerate the investigational agents or be likely to interfere with the study procedures or results
- Subjects who, in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study, or in whom compliance is likely to be suboptimal, should be excluded
- Patients with known active viral hepatitis (i.e. hepatitis A, B, or C)
Additional locations may be listed on ClinicalTrials.gov for NCT05918640.
Locations matching your search criteria
United States
Massachusetts
Boston
Michigan
Ann Arbor
New York
New York
Pennsylvania
Philadelphia
PRIMARY OBJECTIVES:
I. To determine the safety, tolerability, pharmacokinetic profile and recommended phase 2 dose (RP2D) of lurbinectedin given on a day 1, 4 schedule every 21 days in patients with FET fusion tumors. (Phase I)
II. To determine the 6-month progression-free survival (PFS) in patients with Ewing sarcoma treated with lurbinectedin at the recommended phase 2 dose on a day 1, 4 q21d schedule. (Phase II)
SECONDARY OBJECTIVES:
I. To preliminarily evaluate the disease control rate (complete response [CR] +partial response [PR]) per Response Criteria in Solid Tumors (RECIST) 1.1, 6-month PFS, median progression free survival (mPFS), and duration of response in patients with FET-positive tumors treated with lurbinectedin. (Phase I)
II. To determine the disease control rate (CR + PR) per RECIST 1.1, 6-month PFS, mPFS, and duration of response in patients treated with lurbinectedin on a day 1,4 schedule at the RP2D in an exploratory cohort of patients with alternative (non-EWS-FLI1) FET fusions. (Phase I)
III. To determine the median progression-free survival rate for the intention-to-treat population (mPFS), duration of response, overall response rate, and disease control rate (CR + PR) per RECIST 1.1 in patients with Ewing sarcoma treated with lurbinectedin at the recommended phase 2 dose on a day 1, 4 q21d schedule. (Phase II)
EXPLORATORY OBJECTIVES:
I. To determine the relationships between lurbinectedin serum pharmacokinetic (PK) and preclinical modeling as well as disease response. (Phase I)
II. To determine if circulating tumor DNA (ctDNA) correlates with tumor burden and disease response in FET-fusion tumors. (Phase I)
III. To determine the feasibility of capturing circulating tumor cells (CTCs) in FET fusion tumors for transcriptional profiling. (Phase I)
IV. To determine the feasibility of collecting ctDNA to determine chromatin structure in patients with FET fusion proteins. (Phase I)
V. In Ewing sarcoma patients only: To determine if 18F-fluoro-L-thymidine (18F-FLT) positron emission tomography (PET) avidity suppression correlates with tumor burden or disease response. (Phase I)
VI. In Ewing sarcoma patients only: To determine the consequence of lurbinectedin treatment on EWS-FLI1 transcriptional networks. (Phase I)
VII. In DSRCT patients only: To determine the consequence of lurbinectedin treatment on EWS-WT1 transcriptional networks. (Phase I)
VIII. In DSRCT patients only: To determine if fludeoxyglucose F-18 (18F-FDG) PET avidity suppression correlates with tumor burden or disease response as measured by validated response criteria such as PET Response Criteria in Solid Tumors (PERCIST) 1.0. (Phase I)
IX. To determine the feasibility of establishing Patient Derived Xenografts (PDX) in a subset of patients. (Phase I) (Phase I)
X. To determine if 18F-FLT PET avidity suppression correlates with tumor burden or disease response in the subset of patients with Ewing sarcoma. (Phase II)
XI. To determine the consequence of lurbinectedin treatment on EWS-FLI1 transcriptional networks in Ewing sarcoma. (Phase II)
XII. To determine the feasibility of capturing CTCs in Ewing sarcoma patients for transcriptional profiling. (Phase II)
XIII. To determine if ctDNA correlates with tumor burden and disease response in Ewing sarcoma patients. (Phase II)
XIV. To determine the feasibility of collecting ctDNA to determine chromatin structure in patients with Ewing sarcoma. (Phase II)
XV. To determine the feasibility of establishing PDX in a subset of patients. (Phase II)
XVI. To determine if 18F-FDG PET avidity suppression correlates with tumor burden or disease response in DSRCT patients as measured by validated response criteria such as PERCIST 1.0. (Phase II)
OUTLINE:
Patients receive lurbinectedin intravenously (IV) over 1 hour, on days 1 and 4 of each cycle. Cycles repeat every 21 days for up to 28 cycles in the absence of disease progression or unacceptable toxicity. Patients may undergo 18F FLT PET scan during screening and tumor biopsy, computed tomography (CT) scan, magnetic resonance imaging (MRI) and blood sample collection and may undergo bone marrow aspiration and biopsy throughout the study.
After completion of study treatment, patients are followed up at 30 days and then 3, 6, 9, and 12 months, then yearly up to 5 years.
Trial PhasePhase I/II
Trial Typetreatment
Lead OrganizationChildren's Hospital of Philadelphia
Principal InvestigatorTheodore Willis Laetsch
- Primary ID22DT011
- Secondary IDsNCI-2023-06710
- ClinicalTrials.gov IDNCT05918640