Evaluation of LY2606368 Therapy in Combination With Cyclophosphamide or Gemcitabine for Children and Adolescents With Refractory or Recurrent Group 3/Group 4 or SHH Medulloblastoma Brain Tumors

Brain Tumor Clinical Trial

Official title:

St. Jude ELIOT: Phase 1 Evaluation of LY2606368, a Molecularly-Targeted CHK1/2 Inhibitor Therapy, in Combination With Cyclophosphamide or Gemcitabine for Children and Adolescents With Refractory or Recurrent Group 3/Group 4 or SHH Medulloblastoma Brain Tumors

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04023669
• Other study ID #: SJELIOT
• Secondary ID: NCI-2019-04787
• Status: Active, not recruiting
• Phase: Phase 1
• Start date: August 8, 2019
• Est. completion date: October 2024

Study information

• Verified date: March 2024
• Source: St. Jude Children's Research Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

SJELIOT is a phase 1 trial that aims to explore the combination of prexasertib with established DNA-damaging agents used in medulloblastoma to evaluate tolerance and pharmacokinetics in recurrent or refractory disease. Additionally, a small expansion cohort will be incorporated into the trial at the combination MTD/RP2D (maximum tolerated dose/recommended phase two dose) to detect a preliminary efficacy signal.

Stratum A: Prexasertib and Cyclophosphamide

Primary Objectives

• To determine the safety and tolerability and estimate the maximum tolerated dose (MTD)/recommended phase 2 dose (RP2D) of combination treatment with prexasertib and cyclophosphamide in participants with recurrent/refractory Group 3 and Group 4 medulloblastoma and recurrent/refractory sonic hedgehog (SHH) medulloblastoma.

• To characterize the pharmacokinetics of prexasertib in combination with cyclophosphamide.

Secondary Objectives

• To estimate the rate and duration of objective response and progression free survival (PFS) associated with prexasertib and cyclophosphamide treatment in this patient population.

• To characterize the pharmacokinetics of cyclophosphamide and metabolites.

Stratum B: Prexasertib and Gemcitabine

Primary Objectives

• To determine the safety and tolerability and estimate the MTD/RP2D of combination treatment with prexasertib and gemcitabine in participants with recurrent/refractory Group 3 and Group 4 medulloblastoma.

• To characterize the pharmacokinetics of prexasertib in combination with gemcitabine.

Secondary Objectives

• To estimate the rate and duration of objective response and PFS associated with prexasertib and gemcitabine treatment in this patient population.

• To characterize the pharmacokinetics of gemcitabine and gemcitabine triphosphate (only at St. Jude Children's Research Hospital).

Description:

Participants will be stratified by the biological characteristics of their tumor to one of two treatment strata:

STRATUM A

• Combination Treatment: prexasertib and cyclophosphamide

• Patient population: Participants with recurrent/refractory Group 3 and Group 4 (G3/G4) medulloblastoma, recurrent/refractory sonic hedgehog (SHH) medulloblastoma and medulloblastoma participants with Indeterminate molecular subgroup

STRATUM B

• Combination Treatment: prexasertib and gemcitabine

• Patient population: Participants with recurrent/refractory Group 3 and Group 4 medulloblastoma

Participants with a diagnosis of G3/G4 medulloblastoma who qualify for both treatment strata will be assigned per slot availability as well as institutional PI preference. If slots are available in both stratum A and stratum B, patients will be assigned to the dose level nearest completion.

The Rolling 6 design will be used separately in each stratum to estimate the maximum tolerated dose (MTD) or recommended phase two dose (RP2D). Therapy will be administered in cycles of 28 days and may be continued for up to 24 months (26 cycles) in the absence of disease progression or unacceptable toxicity.

Participants will receive doublet therapy in cycles of 28 days. The dose-limiting toxicity (DLT)-evaluation period will consist of the first cycle until day 1 criteria of cycle 2 has been met. Participants will be evaluated at least once a week during the DLT-evaluation period and at regular intervals thereafter. Standard tests (i.e. physical exams, blood tests, and disease evaluations) will be undertaken at regular intervals. Research-associated evaluations (i.e. pharmacokinetic studies, etc.) will also be carried out during therapy. Treatment may be continued for up to 2 years in the absence of disease progression or unacceptable toxicity.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 21
• Est. completion date: October 2024
• Est. primary completion date: May 1, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 1 Year to 24 Years

Eligibility

Inclusion Criteria: Screening Phase

• Participants with recurrent, refractory, or progressive medulloblastoma.

• Age = 1 year and < 25 years at the time of screening.

• Participants and/or guardian can understand and is willing to sign a written informed consent document according to institutional guidelines.

Exclusion Criteria: Screening Phase

• Previous exposure to any CHK1 inhibitor.

• Participants with a history of clinically significant, uncontrolled heart disease and/or repolarization abnormalities.

• Participants with any history of QTc prolongation (i.e. QTc interval of > 480 msec).

Inclusion Criteria: Strata A and B

• Participant must be =1 year and <25 years of age at time of screening.

• Participant must have recurrent, progressive or refractory Group 3/Group 4 or SHH medulloblastoma (per central pathology confirmation of primary tissue and/or relapsed tissue). Central pathology review previously completed at St. Jude Children's Research Hospital using equivalent methods can be used for enrollment. Note: Group 3/Group 4 may be referred to as Non-WNT Non-SHH (NWNS) in pathology reports. Medulloblastoma patients with indeterminate molecular subgroup after central pathology review are eligible for enrollment on stratum A.

• Participant must have measurable or evaluable disease as defined in the protocol.

• Participant must have received their last dose of myelosuppressive anticancer chemotherapy at least 3 weeks prior to study enrollment.

• Participants must have had their last fraction of radiation (including CSI) at least 4 weeks prior to study enrollment. Participants who received radiation therapy for palliation must have had their last fraction of radiation at least 2 weeks prior to study enrollment.

-- Note: Participants must have relapsed with recurrent, progressive or refractory disease after any prior radiation therapy that is not considered palliative. Palliative radiation therapy is defined as local small port RT to alleviate and/or palliate symptoms. (CSI, whole brain RT, large field/port RT, or large field/port multilevel spinal RT will not be considered palliative at any dose.)

• Participant who are receiving corticosteroids must be on a stable or decreasing dose for at least 1 week prior to enrollment with no plans for escalation.

• Participant must have a Lansky (= 16 years) or Karnofsky (> 16 years) performance score of =50 and, in the opinion of the investigator, a minimum life expectancy of at least 6 weeks.

-- Note: Participants who are unable to walk because of paralysis, but who are up in a wheelchair, will be considered ambulatory for the purpose of assessing the performance score.

• Participant must have adequate bone marrow and organ function as defined as:

• ANC = 1.0 x 10^9/L without growth factor support within 7 days

• Platelet count = 75x 10^9/L without support of a platelet transfusion within 7 days

• Hemoglobin =8.0 g/dL without support of a blood transfusion within 7 days

• Potassium, total calcium (corrected for serum albumin), magnesium, sodium and phosphorus within institutional normal limits or corrected to within normal limits with supplements before first dose of study medication

• Serum creatinine = the maximum serum creatinine based on age/gender: Age: 1 to < 2 years; maximum serum creatinine (mg/dL): 0.6 (male, female); Age: 2 to < 6 years; maximum serum creatinine (mg/dL): 0.8 (male, female); Age: 6 to < 10 years; maximum serum creatinine (mg/dL): 1 (male, female); Age: 10 to < 13 years; maximum serum creatinine (mg/dL): 1.2 (male, female); Age: 13 to < 16 years; maximum serum creatinine (mg/dL): 1.5 (male), 1.4 (female); Age := 16 years; maximum serum creatinine (mg/dL): 1.7 (male), 1.4 (female).

• Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) = 2.5 x ULN. For the purposes of this study the ULN of ALT and AST is 45 U/L.

• Total bilirubin = ULN; or if > ULN then direct bilirubin = 1.5 x ULN

• Female participants of childbearing age must have a negative pregnancy test at the time of enrollment.

• Participants of childbearing or child fathering potential must be willing to use medically acceptable form of birth control during treatment and for 16 weeks after stopping treatment.

• Participants and/or guardian have the ability to understand and the willingness to sign a written informed consent document according to institutional guidelines.

Exclusion Criteria: Strata A and B

• Participant who is receiving any other investigational agents.

• Participants with other clinically significant medical disorders (i.e. serious infections or significant cardiac, pulmonary, hepatic, psychiatric, or other organ dysfunction) that could compromise their ability to tolerate protocol therapy or would interfere with the study procedures or results.

• Participant with a history of clinically significant, uncontrolled heart disease and/or repolarization abnormalities as documented by a standard 12-lead ECG.

• Shortening fraction of <27% by ECHO or ejection fraction of <50% by gated radionuclide study.

• Prior history of QTc prolongation or QTc interval of > 480 msec.

• Female participants who are breastfeeding a child.

• Participants are excluded if unable to comply with guidelines listed in appendix I.

Related Conditions & MeSH terms

• Brain Cancer
• Brain Neoplasms
• Brain Tumor
• Brain Tumor, Pediatric
• Brain Tumor, Recurrent
• Brain Tumor, Refractory
• Central Nervous System Neoplasms
• CNS Cancer
• CNS Neoplasm
• CNS Tumor
• Medulloblastoma
• Medulloblastoma Recurrent
• Medulloblastoma, Non-WNT/Non-SHH
• Medulloblastoma, Non-WNT/Non-SHH, Group 3
• Medulloblastoma, Non-WNT/Non-SHH, Group 4
• Neoplasms
• Recurrence

Intervention

Drug:
• Prexasertib
IV
• Cyclophosphamide
IV
• Gemcitabine
IV

Biological:
• filgrastim
Given subcutaneously (SQ). Alternatively, pegfilgrastim may be given.
• peg-filgrastim
Given subcutaneously (SQ). Alternatively, filgrastim may be given.

Locations

Country	Name	City	State
United States	St. Jude Children's Research Hospital	Memphis	Tennessee

Sponsors (2)

Lead Sponsor	Collaborator
St. Jude Children's Research Hospital	Eli Lilly and Company

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Estimate the Maximum tolerated dose (MTD)/Recommended Phase 2 Dose (RP2D) of each doublet by stratum	The maximum tolerated dose (MTD) is empirically defined as the highest dose level at which six patients have been treated with at most one patient experiencing a dose-limiting toxicity (DLT) and the next higher dose level has been determined to be too toxic. The MTD estimate will not be available if the lowest dose level studied is too toxic or the highest dose level studied is considered safe. In the latter case, the highest studied safe dose may be considered as the recommended phase 2 dose (RP2D). The MTD estimation will be limited to evaluable patients and toxicity assessments from course 1 (28 days).	1 month after start of prexasertib and cyclophosphamide or gemcitabine treatment
Primary	To determine the safety and tolerability of combination treatment with prexasertib and cyclophosphamide or gemcitabine.	Incidence of adverse event data at least possibly related to treatment will be summarized in tables by treatment combination and by dose level.	Up to 2 years after start of prexasertib and cyclophosphamide or gemcitabine treatment
Primary	To characterize the area under the concentration-time curve (AUC0-8) of prexasertib in combination with cyclophosphamide or gemcitabine.	Prexasertib area under the curve (AUC0-8) is estimated based on course 1, days 2 through 7 PK samples.	prexasertib and cyclophosphamide or gemcitabine treatment course 1 days 2 through 7
Primary	To characterize the systemic clearance (CL) of prexasertib in combination with cyclophosphamide or gemcitabine.	Prexasertib systemic clearance (CL) is estimated based on course 1, days 2 through 7 pharmacokinetic samples.	prexasertib and cyclophosphamide or gemcitabine treatment course 1 days 2 through 7
Secondary	Rate of objective response (complete or partial response) by stratum	The incidence of objective responses (complete or partial response) observed during prexasertib and cyclophosphamide or gemcitabine treatment or during follow-up prior to progression or initiation of alternative cancer therapy.	Up to 1 year after completion of prexasertib and cyclophosphamide or gemcitabine treatment
Secondary	Duration of objective response by stratum	The duration of objective response is measured from the time the measurement criteria are met for complete response (CR) or partial response (PR), whichever is recorded first, until the first day on which recurrent or progressive disease is objectively documented.	Up to 1 year after completion of prexasertib and cyclophosphamide or gemcitabine treatment
Secondary	Progression-free survival for patients treated with prexasertib and cyclophosphamide or gemcitabine	Progression-free survival (PFS) is defined from the time of treatment initiation until disease progression or until death from any cause (whichever is earlier) for patients who experience an event and until the date of last follow-up for those who are alive and progression free at the time of analysis. PFS is estimated by Kaplan-Meier approach and median PFS is reported.	Up to 3 years from diagnosis
Secondary	To characterize the area under the concentration-time curve (AUC0-24h) of cyclophosphamide.	Cyclophosphamide area under the curve (AUC0-24h) is estimated based on course 1, days 1 and 2 PK samples.	prexasertib and cyclophosphamide treatment course 1, days 1 and 2
Secondary	To characterize the systemic clearance (CL) of cyclophosphamide.	Cyclophosphamide systemic clearance (CL) is estimated based on course 1, days 1 and 2 PK samples.	prexasertib and cyclophosphamide treatment course 1, days 1 and 2
Secondary	To characterize the area under the concentration-time curve (AUC0-24h) of 4-hydroxy-cyclophosphamide.	4-hydroxy-cyclophosphamide are under the curve AUC0-24h is estimated based on course 1, days 1 and 2 PK samples.	prexasertib and cyclophosphamide treatment course 1, days 1 and 2
Secondary	To characterize the area under the concentration-time curve (AUC0-24h) of carboxyethylphosphoramide mustard.	Carboxyethylphosphoramide mustard area under the curve (AUC0-24h) is estimated based on course 1, days 1 and 2. PK samples.	prexasertib and cyclophosphamide treatment course 1, days 1 and 2
Secondary	To characterize the area under the concentration-time curve (AUC0-4h) of gemcitabine.	Gemcitabine area under the curve (AUC0-4h) is estimated based on course 1, day 1 PK samples.	prexasertib and gemcitabine treatment course 1, day 1.
Secondary	To characterize the systemic clearance (CL) of gemcitabine.	Gemcitabine systemic clearance (CL) is estimated based on course 1, day 1 PK samples.	prexasertib and cyclophosphamide treatment course 1, day 1
Secondary	To characterize the area under the concentration-time curve (AUC0-4h) of gemcitabine triphosphate (only at St. Jude Children's Research Hospital).	Gemcitabine triphosphate are under the curve AUC0-4h is estimated based on course 1, day 1 PK samples.	prexasertib and cyclophosphamide treatment course 1, day 1

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