Status:

COMPLETED

CARE Initiative: Real-world Emulation of the KEYNOTE-189 Trial [DS4]

Lead Sponsor:

Aetion, Inc.

Collaborating Sponsors:

AbbVie

Amgen

Conditions:

Metastatic Non Small Cell Lung Cancer

Eligibility:

All Genders

18+ years

Brief Summary

The goal of this non-interventional study is to emulate the KEYNOTE-189 randomized controlled trial of pembrolizumab for the treatment of metastatic non-small cell lung cancer using real-world, electr...

Detailed Description

The Coalition to Advance Real-World Evidence through Randomized Controlled Trial Emulation (CARE) Initiative is a program designed to build an empirical evidence base for the use of real-world data (R...

Eligibility Criteria

Inclusion

  • \- Non-small cell lung cancer (NSCLC) diagnosis
  • Histology not indicative of squamous cell carcinoma
  • Metastatic disease
  • Epidermal growth factor receptor (EGFR) and Anaplastic lymphoma kinase (ALK)-negative or Kirsten rat sarcoma viral oncogene homolog (KRAS)-positive
  • No prior systemic treatment for metastatic NSCLC
  • No record of adjuvant or neoadjuvant therapy in the 12 months before metastatic diagnosis
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or missing or Karnofsky performance status \>=70 or missing
  • No lab results indicating inadequate organ function, as defined in the KEYNOTE-189 RCT protocol

Exclusion

  • Histology indicative of squamous cell carcinoma or small cell elements
  • Receipt of an investigational agent or device in the 4 weeks before study drug initiation
  • Prior systemic treatment for metastatic NSCLC
  • Prior antineoplastic biological therapy
  • History of major cancer-related surgery in the 3 weeks before study drug initiation
  • Radiation therapy to the lung \>30 Gy in the 6 months before study drug initiation
  • Prior diagnosis of clinically active diverticulitis, intra-abdominal abscess, or gastrointestinal obstruction
  • Diagnosis of a second primary malignant neoplasm
  • Diagnosis of brain, central nervous system, and/or spinal cord metastases
  • Diagnosis of rheumatic disease in the 2 years prior to study drug initiation
  • Prior treatment with pembrolizumab or any other anti-PD-1, PD-L1, PDL2 agent or an antibody targeting other immuno-regulatory receptors or mechanisms
  • Diagnosis of human immunodeficiency virus infection

Key Trial Info

Start Date :

February 1 2010

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

April 13 2023

Estimated Enrollment :

304 Patients enrolled

Trial Details

Trial ID

NCT06585189

Start Date

February 1 2010

End Date

April 13 2023

Last Update

September 5 2024

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