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A Study of the Combination of Osimertinib, Platinum and Etoposide for Patients With Metastatic EGFR Mutant Lung Cancers

NCT03567642

Description:

The purpose of this study is to test the safety of combining Osimertinib with either Cisplatin or Carboplatin (at different dose levels) and Etoposide, to find out what effects, if any, this combination of drugs has on people with EGFR mutant lung cancer.

Related Conditions:
  • Non-Small Cell Lung Carcinoma
Recruiting Status:

Recruiting

Phase:

Phase 1

Trial Eligibility

Document

Title

  • Brief Title: A Study of the Combination of Osimertinib, Platinum and Etoposide for Patients With Metastatic EGFR Mutant Lung Cancers
  • Official Title: Phase 1 Study of Combination Osimertinib, Platinum, Etoposide for Patients With Metastatic EGFR Mutant Lung Cancers With Concurrent RB1 and TP53 Alterations

Clinical Trial IDs

  • ORG STUDY ID: 18-211
  • NCT ID: NCT03567642

Conditions

  • Lung Cancer

Interventions

DrugSynonymsArms
OsimertinibOsimertinib, Platinum (cisplatin or carboplatin) and Etoposide
PlatinumOsimertinib, Platinum (cisplatin or carboplatin) and Etoposide
EtoposideOsimertinib, Platinum (cisplatin or carboplatin) and Etoposide

Purpose

The purpose of this study is to test the safety of combining Osimertinib with either Cisplatin or Carboplatin (at different dose levels) and Etoposide, to find out what effects, if any, this combination of drugs has on people with EGFR mutant lung cancer.

Trial Arms

NameTypeDescriptionInterventions
Osimertinib, Platinum (cisplatin or carboplatin) and EtoposideExperimentalInitially, 6 patients will be enrolled and will begin treatment with osimertinib 80mg orally daily (3 who will be receiving cisplatin and 3 who will be receiving carboplatin). Cisplatin or carboplatin treatment will be decided by the treating physician prior to study registration. After 9 weeks (+/- 1 week)( 3 cycles) on osimertinib alone, carboplatin or cisplatin and etoposide will be added. Carboplatin is doses at an AUC of 5 or cisplatin at 60mg/m2 will be given on C4D1. Etoposide is dosed at 100mg/m2 given on Days 1-3 of C4. Only patients on osimertinib 80mg orally daily at the start of cycle 4 will be included in the 3+3 dose de-escalation portion of the study. Chemotherapy and osimertinib will be administered concurrently during cycles 4-7, and from cycle 8 onward, osimertinib monotherapy will be continued.
  • Osimertinib
  • Platinum
  • Etoposide

Eligibility Criteria

        Inclusion Criteria:

          -  Written informed consent

          -  Advanced biopsy-proven metastatic non-small cell lung cancer

          -  Either have not started an EGFR TKI or may have started osimertinib within the last 6
             weeks

          -  Somatic activating mutation in EGFR in pre-treatment tumor biopsy or cfDNA

          -  Evidence of a concurrent P53 alteration by IHC or NGS on pre-treatment tumor biopsy or
             cfDNA

          -  Evidence of a concurrent RB1 alteration by IHC or NGS on pre-treatment tumor biopsy or
             cfDNA

          -  Must have a site of disease amenable to repeat biopsy and be willing to undergo a
             biopsy during treatment

          -  Measurable (RECIST 1.1) indicator lesion not previously irradiated

          -  Karnofsky performance status (KPS) ≥ 70%

          -  Age >18 years old

          -  Ability to swallow oral medication

          -  Adequate organ function

               -  AST, ALT ≤ 3 x ULN

               -  Total bilirubin ≤ 1.5x ULN

               -  Creatinine ≤ 1.5x ULN OR calculated creatinine clearance ≥ 60ml/min

               -  Absolute neutrophil count (ANC) ≥ 1000 cells/mm^3

               -  Hemoglobin≥8.0 g/dL

               -  Platelets ≥100,000/mm^3

        Exclusion Criteria:

          -  Pregnant or lactating women

          -  Started an EGFR TKI other than osimertinib or started osimertinib more than 6 weeks
             ago

          -  Any radiotherapy within 1 week of starting treatment on protocol.

          -  Any major surgery within 1 weeks of starting treatment on protocol.

          -  Any evidence of active clinically significant interstitial lung disease

          -  Continue to have unresolved > grade 1 toxicity from any previous treatment

          -  Have pure small cell histology

          -  HQTc>475msec or any clinically significant (as deemed by the investigator)
             abnormalities in rhythm or conduction or morphology of the resting EKG.

          -  Patients are to be excluded from cisplatin treatment arm if they meet any of the
             following criteria:

          -  Creatinine clearance < 60 ml/min

          -  Hearing impairment requiring assistive device

          -  Neuropathy

          -  The treating provider does not feel as though the patient should receive cisplatin
      
Maximum Eligible Age:N/A
Minimum Eligible Age:18 Years
Eligible Gender:All
Healthy Volunteers:No

Primary Outcome Measures

Measure:The MTD (maximum tolerated dose)
Time Frame:2 years
Safety Issue:
Description:Determine the safety and toxicity profile of combination osimertinib, platinum (cisplatin or carboplatin), etoposide for patients with metastatic EGFR mutant lung cancers with concurrent RB1 and TP53 alterations.

Details

Phase:Phase 1
Primary Purpose:Interventional
Overall Status:Recruiting
Lead Sponsor:Memorial Sloan Kettering Cancer Center

Trial Keywords

  • Osimertinib
  • Platinum
  • Etoposide
  • EGFR Mutant
  • 18-211

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