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Amivantamab compared with real-world therapies in patients with advanced non-small cell lung cancer EGFR Exon 20 insertion mutations after platinum-based chemotherapy.
Kim, Tae Min; Girard, Nicolas; Low, Grace Kah Mun; Zhuo, Jianmin; Yu, Dae Young; Yang, Yishen; Murota, Maiko; Lim, Cindy Thiow Koon; Kleinman, Nora J; Cho, Byoung Chul.
Afiliação
  • Kim TM; Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
  • Girard N; Institut Curie, Institute du Thorax Curie-Montsouris, Paris, France.
  • Low GKM; Medical Affairs, Janssen Asia Pacific Medical Affairs, a division of Johnson & Johnson International (Singapore) Pte. Ltd.
  • Zhuo J; Statistics and Decision Science, Janssen China Research & Development, China.
  • Yu DY; Real World Evidence, Janssen Asia Pacific, Republic of Korea.
  • Yang Y; Statistics and Decision Science, Janssen China Research & Development, China.
  • Murota M; Global Development, Medical Affair Operations, Janssen Research & Development, Tokyo, Japan.
  • Lim CTK; Real World Solutions, IQVIA Solutions Asia Pte Ltd, Singapore.
  • Kleinman NJ; Real World Solutions, IQVIA Hong Kong, Kwai Fong, Hong Kong, P.R. China.
  • Cho BC; Department of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
Acta Oncol ; 62(12): 1689-1697, 2023 Dec.
Article em En | MEDLINE | ID: mdl-37938161
BACKGROUND: In the single-arm CHRYSALIS trial, advanced non-small cell lung cancer patients harboring epidermal growth factor receptor (EGFR) exon 20 insertion (Exon 20ins) showed durable responses to amivantamab, an EGFR-MET bispecific antibody targeting tumors with EGFR Exon 20ins. This study compared the effectiveness of amivantamab to real-world systemic anti-cancer therapies in Japan. PATIENTS AND METHODS: External control patients were selected by applying CHRYSALIS eligibility to Japanese patients from LC-SCRUM-Asia. External control patients were included for every qualifying line of therapy after platinum-based chemotherapy. Propensity score weighting was applied to external control patients to adjust for differences in baseline characteristics. Outcomes were compared between external control patients, and all and Asian-only CHRYSALIS patients using weighted Cox proportional hazards regression models for progression-free survival (PFS), time to next therapy (TTNT), and overall survival (OS), and generalized estimating equations with repeated measurements for overall response rate (ORR). RESULTS: One hundred fifteen CHRYSALIS and 94 external control patients were identified. Compared to external control patients, amivantamab-treated patients had significantly longer OS (median OS 19.88 vs 14.09 months, HR [95% CI] 0.59 [0.40-0.88]), PFS (median PFS 6.74 vs 4.73 months, HR 0.59 [0.45-0.78]), TTNT (median TTNT 12.16 vs 5.09 months, HR 0.39 [0.29-0.53]), and significantly higher ORR (41.7% vs 14.1%). Analyses of amivantamab-treated Asian patients (n = 61) showed similar clinical benefits. CONCLUSION: In the absence of clinical evidence from randomized clinical trials, this study reflects the benefit of amivantamab after platinum-based chemotherapy for advanced non-small cell lung cancer patients harboring EGFR Exon 20ins, compared to current real-world therapies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Idioma: En Ano de publicação: 2023 Tipo de documento: Article