4.7 Article

Phase 1 Dose-Escalation Study of Pegylated Arginine Deiminase, Cisplatin, and Pemetrexed in Patients With Argininosuccinate Synthetase 1-Deficient Thoracic Cancers

Journal

JOURNAL OF CLINICAL ONCOLOGY
Volume 35, Issue 16, Pages 1778-+

Publisher

AMER SOC CLINICAL ONCOLOGY
DOI: 10.1200/JCO.2016.71.3230

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Funding

  1. Cancer Research UK Experimental Cancer Medicine Center at Barts [C16420/A18066, C16420/A15583]
  2. Department of Health, England, via the National Institute for Health Research (NIHR) Biomedical Research Centre
  3. Guy's and St Thomas' NHS Foundation Trust
  4. King's College London
  5. King's College Hospital NHS Foundation Trust (and NIHR Clinical Research Facility)
  6. Spanish Society of Medical Oncology
  7. Higher Education Funding Council for England
  8. Cancer Research UK [16463] Funding Source: researchfish

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PurposePegylated arginine deiminase (ADI-PEG 20) depletes essential amino acid levels in argininosuccinate synthetase 1 (ASS1) -negative tumors by converting arginine to citrulline and ammonia. The main aim of this study was to determine the recommended dose, safety, and tolerability of ADI-PEG 20, cisplatin, and pemetrexed in patients with ASS1-deficient malignant pleural mesothelioma (MPM) or non-small-cell lung cancer (NSCLC).Patients and MethodsUsing a 3 + 3 + 3 dose-escalation study, nine chemotherapy-naive patients (five MPM, four NSCLC) received weekly ADI-PEG 20 doses of 18 mg/m(2), 27 mg/m(2), or 36 mg/m(2), together with pemetrexed 500 mg/m(2) and cisplatin 75 mg/m(2) which were given every three weeks (maximum of six cycles). Patients achieving stable disease or better could continue ADI-PEG 20 monotherapy until disease progression or withdrawal. Adverse events were assessed by Common Terminology Criteria for Adverse Events version 4.03, and pharmacodynamics and immunogenicity were also evaluated. Tumor response was assessed by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 for NSCLC and by modified RECIST criteria for MPM.ResultsNo dose-limiting toxicities were reported; nine of 38 reported adverse events (all grade 1 or 2) were related to ADI-PEG 20. Circulating arginine concentrations declined rapidly, and citrulline levels increased; both changes persisted at 18 weeks. Partial responses were observed in seven of nine patients (78%), including three with either sarcomatoid or biphasic MPM.ConclusionTarget engagement with depletion of arginine was maintained throughout treatment with no dose-limiting toxicities. In this biomarker-selected group of patients with ASS1-deficient cancers, clinical activity was observed in patients with poor-prognosis tumors. Therefore, we recommend a dose for future studies of weekly ADI-PEG 20 36 mg/m(2) plus three-weekly cisplatin 75 mg/m(2) and pemetrexed 500 mg/m(2).

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