Osimertinib or Platinum–Pemetrexed in <i>EGFR</i> T790M–Positive Lung Cancer

Осимертиниб или платино-пеметрексед при раке легкого с мутацией EGFR T790M
Tony Mok, Frances A. Shepherd, Marcelo Marotti, Suresh S. Ramalingam, Vassiliki A. Papadimitrakopoulou, Marina Chiara Garassino, Martin Sebastian, Helen Mann, Chee Khoon Lee, Serban Ghiorghiu, Yi‐Long Wu, Myung‐Ju Ahn, Hye Ryun Kim, Yong He, Hiroaki Akamatsu, Willemijn S.M.E. Theelen, Alison Templeton
2016-12-06

EGFR T790M-positive lung cancerNon-small-cell lung cancerOsimertinibPlatinum-pemetrexed therapyProgression-free survival
BACKGROUND: Osimertinib is an epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) that is selective for both EGFR-TKI sensitizing and T790M resistance mutations in patients with non-small-cell lung cancer. The efficacy of osimertinib as compared with platinum-based therapy plus pemetrexed in such patients is unknown. METHODS: In this randomized, international, open-label, phase 3 trial, we assigned 419 patients with T790M-positive advanced non-small-cell lung cancer, who had disease progression after first-line EGFR-TKI therapy, in a 2:1 ratio to receive either oral osimertinib (at a dose of 80 mg once daily) or intravenous pemetrexed (500 mg per square meter of body-surface area) plus either carboplatin (target area under the curve, 5 [AUC5]) or cisplatin (75 mg per square meter) every 3 weeks for up to six cycles; maintenance pemetrexed was allowed. In all the patients, disease had progressed during receipt of first-line EGFR-TKI therapy. The primary end point was investigator-assessed progression-free survival. RESULTS: The median duration of progression-free survival was significantly longer with osimertinib than with platinum therapy plus pemetrexed (10.1 months vs. 4.4 months; hazard ratio; 0.30; 95% confidence interval [CI], 0.23 to 0.41; P<0.001). The objective response rate was significantly better with osimertinib (71%; 95% CI, 65 to 76) than with platinum therapy plus pemetrexed (31%; 95% CI, 24 to 40) (odds ratio for objective response, 5.39; 95% CI, 3.47 to 8.48; P<0.001). Among 144 patients with metastases to the central nervous system (CNS), the median duration of progression-free survival was longer among patients receiving osimertinib than among those receiving platinum therapy plus pemetrexed (8.5 months vs. 4.2 months; hazard ratio, 0.32; 95% CI, 0.21 to 0.49). The proportion of patients with adverse events of grade 3 or higher was lower with osimertinib (23%) than with platinum therapy plus pemetrexed (47%). CONCLUSIONS: Osimertinib had significantly greater efficacy than platinum therapy plus pemetrexed in patients with T790M-positive advanced non-small-cell lung cancer (including those with CNS metastases) in whom disease had progressed during first-line EGFR-TKI therapy. (Funded by AstraZeneca; AURA3 ClinicalTrials.gov number, NCT02151981 .).
1
Among patients with central nervous system metastases, osimertinib prolonged median progression-free survival compared with platinum–pemetrexed: 8.5 versus 4.2 months.
2
Grade 3 or higher adverse events occurred less frequently with osimertinib than with platinum–pemetrexed chemotherapy: 23% versus 47%.
3
In EGFR T790M-positive advanced non-small-cell lung cancer progressing after first-line EGFR-TKI therapy, osimertinib significantly prolonged progression-free survival versus platinum–pemetrexed chemotherapy.
4
Median progression-free survival was 10.1 months with osimertinib versus 4.4 months with platinum–pemetrexed (hazard ratio, 0.30; P<0.001).
5
Osimertinib produced a significantly higher objective response rate than platinum–pemetrexed: 71% versus 31% (odds ratio, 5.39; P<0.001).

Patients with T790M-positive advanced non-small-cell lung cancer whose disease progressed after first-line EGFR-TKI therapy

Comparative efficacy and safety of osimertinib versus platinum–pemetrexed therapy, including progression-free survival, objective response, CNS disease control, and grade ≥3 adverse events

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2016-12-06
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Authors
Tony Mok
Frances A. Shepherd
Marcelo Marotti
Suresh S. Ramalingam
Vassiliki A. Papadimitrakopoulou
Marina Chiara Garassino
Martin Sebastian
Helen Mann
Chee Khoon Lee
Serban Ghiorghiu
Yi‐Long Wu
Myung‐Ju Ahn
Hye Ryun Kim
Yong He
Hiroaki Akamatsu
Willemijn S.M.E. Theelen
Alison Templeton
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