A Study of Atezolizumab as First-line Monotherapy for Advanced or Metastatic Non-Small Cell Lung Cancer

  • Non-Small Cell Lung Cancer
Trial Status:

Completed

This trial runs in
Cities
  • Charlotte
  • Cleveland
  • Dallas
  • Falls Church
  • Farmington
  • Fresno
  • Hoffman Estates
  • Hollywood
  • Indianapolis
  • Lacey
  • Madison
  • Minneapolis
  • New York
  • Orlando
  • Philadelphia
  • Quincy
  • Sioux Falls
  • Stony Brook
  • Wichita
  • Ypsilanti
Trial Identifier:

NCT02848651 ML39237

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      The source of the below information is the publicly available website ClinicalTrials.gov. It has been summarised and edited into simpler language.

      The below information is taken directly from the publicly available website ClinicalTrials.gov within a week of any updates, and has not been edited.

      Results Disclaimer

      Trial Summary

      This was a Phase II, open-label, prospective, multicenter study designed to evaluate the efficacy and safety of single-agent atezolizumab as a first-line therapy in participants with locally advanced or metastatic non-small cell lung cancer (NSCLC). In addition, the primary biomarker objective was to measure blood tumor mutational burden (bTMB) and evaluate whether it can predict for improved clinical outcome with atezolizumab.

      Genentech, Inc. Sponsor
      Phase 2 Phase
      NCT02848651 , ML39237 Trial Identifier
      Atezolizumab Treatments
      Non-Small Cell Lung Cancer Condition
      Official Title

      A Phase II Single-Arm Study of Atezolizumab Monotherapy in Locally Advanced or Metastatic Non-Small Cell Lung Cancer: Clinical Evaluation of Novel Blood-Based Diagnostics

      Eligibility Criteria

      All Gender
      ≥18 Years Age
      No Healthy Volunteers
      Inclusion Criteria
      • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
      • Histologically or cytologically confirmed Stage IIIB-IVB NSCLC
      • For participants who have received prior neo-adjuvant/adjuvant chemotherapy or chemoradiotherapy with curative intent for non-metastatic disease: a treatment-free interval of at least 6 months prior to enrollment
      • Participants with any programmed death-ligand 1 (PD-L1) test result by immunohistochemistry (IHC) are eligible for the study
      • Participants without a PD-L1 test result are eligible for the study
      • Measurable disease per RECIST v1.1
      • Adequate hematologic and end-organ function
      • Agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive methods among women of childbearing potential
      Exclusion Criteria
      • Prior treatment with immunotherapy for any stage NSCLC, including early-stage (neoadjuvant or adjuvant) disease
      • Participants with epidermal growth factor receptor (EGFR) sensitizing mutations and anaplastic lymphoma kinase (ALK) rearrangements
      • Active central nervous system (CNS) metastases requiring treatment
      • Spinal cord compression not definitively treated or not clinically stable
      • Leptomeningeal disease
      • Uncontrolled tumor-related pain
      • Uncontrolled pleural, pericardial effusions, or ascites requiring recurrent drainage procedures
      • Uncontrolled or symptomatic hypercalcemia
      • Malignancies other than NSCLC within 5 years prior to enrollment, except for those curatively treated with negligible risk of metastasis or death
      • Pregnant or lactating women
      • History of autoimmune disease, significant pulmonary disease, or significant cardiovascular disease
      • Positive human immunodeficiency virus (HIV) or hepatitis B or C
      • Active tuberculosis
      • Severe infection or major surgery within 4 weeks, or oral or IV antibiotics treatment within 2 weeks prior to enrollment
      • Prior treatment with or hypersensitivity to study drug or related compounds
      • Prior allogeneic bone marrow or solid organ transplant
      • Administration of a live, attenuated vaccine within 4 weeks prior to enrollment
      • Treatment with systemic immunostimulatory agents within 4 weeks or 5 half-lives of the drug (whichever is longer) prior to enrollment
      • Treatment with systemic corticosteroids or other systemic immunosuppressive medications within 2 weeks prior to enrollment

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