Real-world global data on targeting epidermal growth factor receptor mutations in stage III non-small-cell lung cancer: the results of the KINDLE study

Author:

Jazieh Abdul Rahman1,Onal Huseyin Cem2,Tan Daniel Shao-Weng3,Soo Ross A.4,Prabhash Kumar5,Kumar Amit6,Huggenberger Reto7,Cho Byoung Chul8ORCID

Affiliation:

1. Cincinnati Cancer Advisors, Cincinnati, OH, USA

2. Department of Radiation Oncology, Adana Dr. Turgut Noyan Research and Treatment Centre, Baskent University, Adana, Turkey

3. Division of Medical Oncology, National Cancer Centre, Singapore

4. National University Cancer Institute, Level 7 NUHS Tower Block, 1E Kent Ridge Road, Singapore 119228, Singapore

5. Department of Medical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India

6. AstraZeneca Pharma India Ltd, Bangalore, Karnataka, India

7. AstraZeneca, Switzerland

8. Yonsei University College of Medicine, Seoul, Republic of Korea

Abstract

Background: Tyrosine kinase inhibitors (TKIs) are the standard of care for resectable and metastatic non-small-cell lung cancer (NSCLC) harbouring epidermal growth factor receptor (EGFR) mutations (EGFRm). We describe the real-world practice of EGFRm testing, prevalence, treatment and outcomes in EGFRm stage III NSCLC from a multi-country, observational study. Methods: The KINDLE study retrospectively captured diagnostic information, treatments and survival outcomes in patients with stage III NSCLC from January 2013 to December 2017. Baseline characteristics and treatments were described and real-world outcomes from initial therapy were analysed using Kaplan–Meier methods. Results: A total of 3151 patients were enrolled across three regions: Asia ( n = 1874), Middle East and North Africa (MENA) ( n = 1046) and Latin America (LA) ( n = 231). Of these, 1114 patients (35%) were tested for EGFRm (46% in Asia, 17% in MENA and 32% in LA) and EGFRm was detected in 32% of tested patients (34.3% in Asia, 20.0% in MENA and 28.4% in LA). In a multi-variate analysis, overall EGFRm patients treated with EGFR-TKI monotherapy as initial treatment, without any irradiation, had twice the risk of dying (hazard ratio: 1.983, 95% confidence interval: 1.079–3.643; p = 0.027) versus any other treatment. Finally, unresectable patients with EGFRm NSCLC who received concurrent chemoradiotherapy (cCRT) as initial therapy had longer overall survival (OS) compared with their counterparts who only received TKI monotherapy without any irradiation (48 months versus 24 months; p < 0.001). Conclusion: The KINDLE study showed that a minority of stage III NSCLC patients were tested for EGFRm. Patients with EGFRm with unresectable NSCLC had similar outcomes from cCRT as initial therapy compared with EGFR wild type with a trend in OS favouring the EGFRm group. Outcomes with EGFR-TKI monotherapy as initial therapy, without any irradiation, were worse. The ongoing LAURA study (NCT03521154) will help define the role of EGFR-TKIs in EGFRm stage III NSCLC treated with cCRT. Trial Registration: NCT03725475.

Publisher

SAGE Publications

Subject

Oncology

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