Neoadjuvant (neoadj) osimertinib (osi) ± chemotherapy (CT) vs CT alone in resectable (R) epidermal growth factor receptor-mutated (EGFRm) NSCLC: NeoADAURA.

J Jamie E. Chaft (Department of Medicine, Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY) W Walter Weder J 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) K Keneng Chen (Department I of Thoracic Surgery, Peking University Cancer Hospital and Institute, Beijing) M Maximilian Hochmair (Karl Landsteiner Institute for Lung Research and Pulmonary Oncology, Klinik Floridsdorf, Vienna) J Jin-Yuan Shih (Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan) S Sung Yong Lee K Kang-Yun Lee N Nguyen Nhung (Vietnam National Lung Hospital, Faculty of Medicine, UMP, VNU, Hanoi, Viet Nam) S Somcharoen Saeteng C Carlos Henrique Andrade Teixeira (Hospital Alemão Oswaldo Cruz, São Paulo, Brazil and Grupo Brasileiro de Oncologia Torácica (GBOT), Porto Alegre, Brazil) C Carles Escriu (Department of Medical Oncology, Clatterbridge Cancer Centre National Health Service Foundation Trust, Liverpool, United Kingdom) A Alex Martinez-Marti (Department of Medical Oncology, Vall d’Hebron Institute of Oncology (VHIO), Vall d’Hebron University Hospital, Barcelona, Spain) C Collin M. Blakely Y Yasushi Yatabe S Sanja Dacic (Department of Pathology, Yale School of Medicine, New Haven, CT) X Xiangning Huang (Biometrics, Late-stage Development, Oncology R&D, AstraZeneca, Cambridge, United Kingdom) Y Yuri Rukazenkov (Oncology Research and Development, AstraZeneca, Cambridge, United Kingdom) A Anupriya Dayal (Late-stage Development, Oncology R&D, AstraZeneca, Gaithersburg, MD) M Masahiro Tsuboi (National Cancer Center Hospital East, Kashiwa, Japan)

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

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 8001-8001
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

J

Jamie E. Chaft

Department of Medicine, Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY

W

Walter Weder

J

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

K

Keneng Chen

Department I of Thoracic Surgery, Peking University Cancer Hospital and Institute, Beijing

M

Maximilian Hochmair

Karl Landsteiner Institute for Lung Research and Pulmonary Oncology, Klinik Floridsdorf, Vienna

J

Jin-Yuan Shih

Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan

S

Sung Yong Lee

K

Kang-Yun Lee

N

Nguyen Nhung

Vietnam National Lung Hospital, Faculty of Medicine, UMP, VNU, Hanoi, Viet Nam

S

Somcharoen Saeteng

C

Carlos Henrique Andrade Teixeira

Hospital Alemão Oswaldo Cruz, São Paulo, Brazil and Grupo Brasileiro de Oncologia Torácica (GBOT), Porto Alegre, Brazil

C

Carles Escriu

Department of Medical Oncology, Clatterbridge Cancer Centre National Health Service Foundation Trust, Liverpool, United Kingdom

A

Alex Martinez-Marti

Department of Medical Oncology, Vall d’Hebron Institute of Oncology (VHIO), Vall d’Hebron University Hospital, Barcelona, Spain

C

Collin M. Blakely

Y

Yasushi Yatabe

S

Sanja Dacic

Department of Pathology, Yale School of Medicine, New Haven, CT

X

Xiangning Huang

Biometrics, Late-stage Development, Oncology R&D, AstraZeneca, Cambridge, United Kingdom

Y

Yuri Rukazenkov

Oncology Research and Development, AstraZeneca, Cambridge, United Kingdom

A

Anupriya Dayal

Late-stage Development, Oncology R&D, AstraZeneca, Gaithersburg, MD

M

Masahiro Tsuboi

National Cancer Center Hospital East, Kashiwa, Japan