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Phase 3 N=595 Randomized Treatment

A Global Study to Assess the Effects of MEDI4736 (Durvalumab), Given as Monotherapy or in Combination With Tremelimumab Determined by PD-L1 Expression Versus Standard of Care in Patients With Locally Advanced or Metastatic Non Small Cell Lung Cancer

Non - Small Cell Lung Cancer NSCLC

Enrolled (actual)
595
Serious AEs
32.7%
Results posted
Apr 2019
Primary outcome: Primary: Overall Survival (OS) — 11.7; 6.8; 11.5; 8.7 months — p=0.109

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
MEDI4736 (durvalumab) (Drug); Vinorelbine (Drug); Gemcitabine (Drug); Erlotinib (Drug); MEDI4736 (durvalumab) in combination with tremelimumab (anti-CTLA4) (Drug); tremelimumab (anti-CTLA4) (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
AstraZeneca
Primary completion
Feb 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Survival (OS)
11.7; 6.8; 11.5; 8.7 0.109
PRIMARY
Progression-Free Survival (PFS)
3.8; 2.2; 3.5; 3.5 0.056
SECONDARY
OS, Contribution of the Components Analysis of Sub-study B
11.5; 10.0; 6.9 0.885
SECONDARY
Percentage of Participants Alive at 12 Months (OS12)
49.3; 31.3; 49.5; 38.8; 43.6; 41.2 0.063
SECONDARY
PFS, Contribution of the Components Analysis of Sub-study B
3.5; 3.1; 2.1 0.282
SECONDARY
Objective Response Rate (ORR)
35.5; 12.5; 14.9; 6.8; 15.4; 6.7 0.037 sig
SECONDARY
Duration of Response (DoR)
9.5; 4.8; 12.2; 10.8; 10.0; 4.7
SECONDARY
Percentage of Participants Alive and Progression Free at 6 Months (APF6)
35.5; 24.1; 31.5; 27.6; 27.2; 14.5
SECONDARY
Percentage of Participants Alive and Progression Free at 12 Months (APF12)
19.4; 9.9; 20.6; 8.0; 15.0; 7.3
SECONDARY
Time From Randomisation to Second Progression (PFS2) of Sub-study B
9.1; 6.7; 8.0; 5.7 0.002 sig

Summary

This study is a Phase III, randomised, open label, multi-centre study assessing the efficacy and safety of MEDI4736 (durvalumab) versus Standard of Care in NSCLC patients with PD-L1 positive tumours and the combination of MEDI4736 (durvalumab) plus tremelimumab (MEDI4736+treme) versus Standard of Care in NSCLC patients with PD-L1-negative tumours in the treatment of male and female patients with locally advanced or metastatic NSCLC (Stage IIIB-IV), who have received at least 2 prior systemic treatment regimens including 1 platinum-based chemotherapy regimen for NSCLC. Patients with known EGFR (Epidermal growth factor receptor) tyrosine kinase (TK) activating mutations and anaplastic lymphoma kinase (ALK) rearrangements are not eligible for the study (prospective testing is not planned within this study). The Standard of Care options are: an EGFR tyrosine kinase inhibitor (erlotinib [TARCEVA®]), gemcitabine or vinorelbine (NAVELBINE®)

Eligibility Criteria

Inclusion Criteria

  • Aged at least 18 years
  • Documented evidence of NSCLC (Stage IIIB/ IV disease)
  • Disease progression or recurrence after both a platinum-based chemotherapy regimen and at least 1 additional regimen for treatment of NSCLC
  • World Health Organization (WHO) Performance Status of 0 or 1
  • Estimated life expectancy more than 12 weeks

Exclusion Criteria

  • Prior exposure to any anti-PD-1 or anti-PD-L1 antibody or anti-CTLA4
  • Brain metastases or spinal cord compression unless asymptomatic, treated and stable (not requiring steroids)
  • Active or prior documented autoimmune disease within the past 2 years
  • Evidence of severe or uncontrolled systemic disease, including active bleeding diatheses or active infections including hepatitis B, C and HIV
  • Any unresolved toxicity CTCAE (Common Terminology Criteria of Adverse Events) >Grade 2 from previous anti-cancer therapy
  • Known EGFR TK activating mutations or ALK rearrangements
  • Any prior Grade ≥3 immune-related adverse event (irAE) while receiving any previous immunotherapy agent, or any unresolved irAE >Grade 1
  • Active or prior documented inflammatory bowel disease (eg, Crohn's disease, ulcerative colitis)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02352948). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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