CAMPFIRE: A Study of Abemaciclib (LY2835219) in Participants With Ewing's Sarcoma

Lilly

Status and phase: Active, not recruiting; Phase 2

Conditions: Neoplasm Metastasis; Sarcoma, Ewing

Treatments: Drug: Temozolomide; Drug: Irinotecan; Drug: Abemaciclib

Study type: Interventional

Funder types: Industry

Identifiers

NCT05440786

2023-506772-28-00 (EU Trial (CTIS) Number)

18434

J1S-MC-JP04 (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to measure the benefit of adding abemaciclib to chemotherapy (irinotecan and temozolamide) for Ewing's sarcoma that has come back or did not respond to treatment. This trial is part of the CAMPFIRE master protocol, which is a platform to speed development of new treatments for children and young adults with cancer. Your participation in this trial could last 11 months or longer, depending on how you and your tumor respond.

Enrollment: 45 estimated patients

Sex: All

Ages: 1 to 39 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Diagnosis of Ewing's sarcoma or Ewing's sarcoma-like tumor by institutional pathologist. The original pathological report is required. Repeat biopsy at progression is not required

• Refractory disease or confirmed radiological progression or recurrence following first or later line of treatment of Ewing's sarcoma or Ewing's sarcoma-like tumor

  -- Must have one measurable or evaluable lesion per RECIST 1.1

• Adequate performance status based on age

  • For participants less than (<)16 years of age, a Lansky score greater than or equal to (≥)50, or
  • For participants ≥16 years of age, a Karnofsky score ≥50

• Participants must have discontinued all previous treatments for cancer or investigational agents ≥7 days after the last dose and must have recovered from the acute effects

• Adequate hematologic and organ function less than or equal to (≤)14 days prior to Day 1 of Cycle 1:

  • Absolute neutrophil count ≥1000/microliter (µL)
  • Platelets ≥75,000/cubic millimeter (mm³)
  • Hemoglobin ≥8 grams per deciLiter (g/Dl) (≥100 grams per Liter [g/L])
  • Total bilirubin ≤1.5 times (×) upper limit of normal (ULN)
  • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤3 × ULN
  • Creatinine clearance or calculated glomerular filtration rate (GFR) ≥60 milliliters per minute per square meter (Ml/min/m²) or serum creatinine based on age/gender

• Female participants of childbearing potential must have a negative urine or serum pregnancy test

• Body weight ≥10 kilograms (kg)

• Must be able to swallow and/or have a gastric/nasogastric tube

  -- Participants in the European Union must be able to swallow intact capsules

• Stable or decreasing dose of steroids at least 7 days prior to enrollment

• Life expectancy of at least 8 weeks and able to complete at least 1 cycle of treatment

• Participants/caregivers are able and willing to make themselves available for the duration of the study and are willing to follow study procedures, including adherence to the pharmacokinetic (PK) sampling schedule

Exclusion criteria

• Participants with severe and/or uncontrolled concurrent medical disease or psychiatric illness/social situation that in the opinion of the investigator could cause unacceptable safety risks or compromise compliance with the protocol

• Participants with an active fungal, bacterial, and/or known severe viral infection including, but not limited to, human immunodeficiency virus (HIV) or viral (A, B, or C) hepatitis.

• Participants who have had allogeneic bone marrow or solid organ transplant

• Surgery: Participants who have had, or are planning to have, the following invasive procedures:

  • Major surgical procedure, laparoscopic procedure, or significant traumatic injury within 28 days prior to enrollment
  • Surgical or other wounds must be adequately healed prior to enrollment

• Female participants who are pregnant or breastfeeding

• Have received any prior cyclin-dependent kinase (CDK) 4 and 6 inhibitor

• Progression during prior treatment with irinotecan and/or temozolomide

• Have a known intolerability or hypersensitivity to any of the study treatments or dacarbazine

• Diagnosed and/or treated additional malignancy within 3 years prior to enrollment

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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45 participants in 2 patient groups

Abemaciclib + Irinotecan +Temozolomide

Experimental group

Description:

Abemaciclib given orally in combination with irinotecan given IV and temozolomide given orally.

Treatment:

Drug: Abemaciclib

Drug: Irinotecan

Drug: Temozolomide

Irinotecan +Temozolomide

Experimental group

Description:

Irinotecan given IV and temozolomide orally.

Treatment:

Drug: Irinotecan

Drug: Temozolomide