Neoadjuvant (neoadj) osimertinib (osi) ± chemotherapy (CT) vs CT alone in resectable (R) epidermal growth factor receptor-mutated (EGFRm) NSCLC: NeoADAURA.
Abstract
8001 Background: Based on the Ph 3 ADAURA study, adjuvant (adj) treatment (Tx) with osi, a 3rd-generation, EGFR-TKI, is SoC for resected EGFRm stage (stg) IB–IIIA NSCLC (AJCC 7th ed). Neoadj Tx may improve surgical and long-term outcomes. NeoADAURA (NCT04351555) is a global, Ph 3, randomized, controlled, 3-arm study assessing outcomes with neoadj osi ± CT vs CT alone, in EGFRm R-NSCLC. Methods: Eligible pts: aged ≥18 yrs; WHO PS ≤1; EGFRm (Ex19del/L858R) stg II–IIIB (AJCC 8th ed) R-NSCLC. Pts were stratified (stg II vs III; non-Asian vs Chinese vs other Asian; Ex19del vs L858R) and randomized 1:1:1 to neoadj osi 80 mg QD (≥9 wks) + CT (cis/carboplatin + pemetrexed; 3 cycles, Q3W), osi monotherapy (mono) 80 mg QD (≥9 wks) or placebo (PBO) QD + CT (3 cycles, Q3W). Osi/PBO + CT: double blind; osi mono: open label, sponsor blind. Adj osi was offered to all pts who completed surgery (Sx). Primary endpoint: major pathological response (MPR) by blinded central pathology review. Secondary endpoints included pathological complete response (pCR), event-free survival (EFS), and safety. Data cut-off: Oct 15, 2024. Results: Overall, 358 pts were randomized: osi + CT n=121/osi mono n=117/PBO + CT n=120; baseline characteristics were generally balanced across the respective arms (stg II: 49%/50%/51%; non-Asian: 27%/26%/25%; Ex19del: 50%/51%/51%). After neoadj Tx, 92%/97%/89% of pts underwent Sx in the osi + CT/osi mono/PBO + CT arms. Osi + CT (MPR rate 26%) and osi mono (25%) showed statistically significant improvement in MPR vs PBO + CT (2%): odds ratios were 19.8 (p<0.0001) and 19.3 (p<0.0001), respectively. Interim EFS (15% maturity) trended in favor of osi + CT and osi mono vs PBO + CT (Table); ≥80% of pts in each arm received adj osi. In the neoadj period, grade ≥3 all-cause AEs and AEs leading to discontinuation of any Tx occurred in 36%/13%/33% and 9%/3%/5% of pts, respectively, for osi + CT/osi mono/PBO + CT. No pts died within 30 days of Sx. Conclusions: Neoadj osi with or without CT showed statistically significant improvement in the MPR rate over CT alone. EFS data were immature and trended in favor of the osi containing arms. There were no new safety concerns. Neoadj osi ± CT should be considered when planning Tx for pts with EGFRm stg II–IIIB R-NSCLC. Clinical trial information: NCT04351555 . Osi + CT (n=121) Osi mono(n=117) PBO + CT(n=120) MPR rate, % (95% CI)Difference vs PBO + CT, % (95% CI)Odds ratio vs PBO + CT (adjusted 100×[1−alpha]% CI)p-value 26 (18, 34)24 (15, 32)19.8 (4.6, 85.3 a ) <0.0001 25 (17, 34)23 (15, 32)19.3 (1.7, 217.4 b ) <0.0001 2 (<1, 6)––– pCR rate, % (95% CI) 4 (1, 9) 9 (4, 15) 0 (0, 3) 12-mo EFS rate, % (95% CI)EFS hazard ratio vs PBO + CT (CI)p-valueMedian EFS follow-up, mos (range) f 93 (87, 97)0.50 (0.17, 1.41 c ) 0.0382 e 16 (0–42) 95 (89, 98)0.73 (0.40, 1.35 d ) –18 (2–42) 83 (75, 89)––19 (2–42) a 95.002% CI; b 99.9% CI; c 99.8% CI; d 95% CI; e p-value ≤0.002 required for statistical significance at interim analysis; f censored pts.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Jamie E. Chaft
Department of Medicine, Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY
Walter Weder
Jianxing He
State Key Laboratory of Respiratory Disease National Clinical Research Center for Respiratory Disease National Center for Respiratory Medicine Guangzhou Institute of Respiratory Health Guangzhou China
Keneng Chen
Department I of Thoracic Surgery, Peking University Cancer Hospital and Institute, Beijing
Maximilian Hochmair
Karl Landsteiner Institute for Lung Research and Pulmonary Oncology, Klinik Floridsdorf, Vienna
Jin-Yuan Shih
Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan
Sung Yong Lee
Kang-Yun Lee
Nguyen Nhung
Vietnam National Lung Hospital, Faculty of Medicine, UMP, VNU, Hanoi, Viet Nam
Somcharoen Saeteng
Carlos Henrique Andrade Teixeira
Hospital Alemão Oswaldo Cruz, São Paulo, Brazil and Grupo Brasileiro de Oncologia Torácica (GBOT), Porto Alegre, Brazil
Carles Escriu
Department of Medical Oncology, Clatterbridge Cancer Centre National Health Service Foundation Trust, Liverpool, United Kingdom
Alex Martinez-Marti
Department of Medical Oncology, Vall d’Hebron Institute of Oncology (VHIO), Vall d’Hebron University Hospital, Barcelona, Spain
Collin M. Blakely
Yasushi Yatabe
Sanja Dacic
Department of Pathology, Yale School of Medicine, New Haven, CT
Xiangning Huang
Biometrics, Late-stage Development, Oncology R&D, AstraZeneca, Cambridge, United Kingdom
Yuri Rukazenkov
Oncology Research and Development, AstraZeneca, Cambridge, United Kingdom
Anupriya Dayal
Late-stage Development, Oncology R&D, AstraZeneca, Gaithersburg, MD
Masahiro Tsuboi
National Cancer Center Hospital East, Kashiwa, Japan