Your browser doesn't support javascript.
loading
CNS Efficacy of Osimertinib With or Without Chemotherapy in Epidermal Growth Factor Receptor-Mutated Advanced Non-Small-Cell Lung Cancer.
Jänne, Pasi A; Planchard, David; Kobayashi, Kunihiko; Cheng, Ying; Lee, Chee Khoon; Valdiviezo, Natalia; Laktionov, Konstantin; Yang, Tsung-Ying; Yu, Yan; Kato, Terufumi; Jiang, Liyan; Chewaskulyong, Busyamas; Lucien Geater, Sarayut; Maurel, Jean-Marc; Rojas, Carlos; Takahashi, Toshiaki; Havel, Libor; Shepherd, Frances A; Tanaka, Kentaro; Ghiorghiu, Dana; Amin, Neha P; Armenteros-Monterroso, Elena; Huang, Xiangning; Chaudhry, Ammar Ahmed; Yang, James Chih-Hsin.
Afiliação
  • Jänne PA; Department of Medical Oncology, Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Planchard D; Department of Medical Oncology, Thoracic Group and International Center for Thoracic Cancers (CICT), Gustave Roussy, Villejuif, France.
  • Kobayashi K; Faculty of Medicine, Paris-Saclay University, Paris, France.
  • Cheng Y; Department of Respiratory Medicine, Saitama Medical University International Medical Center, Hidaka, Japan.
  • Lee CK; Department of Thoracic Oncology, Jilin Cancer Hospital, Changchun, China.
  • Valdiviezo N; Department of Medical Oncology, Cancer Care Centre, St George Hospital, Kogarah, NSW, Australia.
  • Laktionov K; Department of Oncology, Instituto Nacional de Enfermedades Neoplasicas, Lima, Peru.
  • Yang TY; Federal State Budgetary Institution "N.N.Blokhin National Medical Research Center of Oncology" of the Ministry of Health of the Russian Federation, Moscow, Russia.
  • Yu Y; Division of Chest Medicine, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
  • Kato T; Department of Life Sciences, National Chung Hsing University, Taichung, Taiwan.
  • Jiang L; Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.
  • Chewaskulyong B; Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japan.
  • Lucien Geater S; Department of Respiratory Medicine, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China.
  • Maurel JM; Division of Oncology, Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
  • Rojas C; Department of Internal Medicine, Prince of Songkla University, Songkhla, Thailand.
  • Takahashi T; Department of Clinical Oncology, Rondebosch Oncology Centre, Cape Town, South Africa.
  • Havel L; Medical Oncology Department, Bradford Hill Clinical Research Center, Santiago, Chile.
  • Shepherd FA; Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
  • Tanaka K; First Faculty of Medicine, Charles University, Thomayer Hospital, Prague, Czech Republic.
  • Ghiorghiu D; Department of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, ON, Canada.
  • Amin NP; Research Institute for Diseases of the Chest, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Armenteros-Monterroso E; Late Development Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Huang X; Late Development Oncology, AstraZeneca, Gaithersburg, MD.
  • Chaudhry AA; Late Development Oncology, AstraZeneca, Cambridge, United Kingdom.
  • Yang JC; Department of Oncology Biometrics, AstraZeneca, Cambridge, United Kingdom.
J Clin Oncol ; 42(7): 808-820, 2024 Mar 01.
Article em En | MEDLINE | ID: mdl-38042525
ABSTRACT

PURPOSE:

We report CNS efficacy of first-line osimertinib plus chemotherapy versus osimertinib monotherapy in patients with epidermal growth factor receptor (EGFR)-mutated advanced non-small-cell lung cancer (NSCLC) from the phase III FLAURA2 study according to baseline CNS metastasis status.

METHODS:

Patients were randomly assigned to osimertinib plus platinum-pemetrexed (combination) or osimertinib monotherapy until disease progression or discontinuation. Brain scans were performed in all patients at baseline and progression and at scheduled assessments until progression for patients with baseline CNS metastases; scans were assessed by neuroradiologist CNS blinded independent central review (BICR).

RESULTS:

On the basis of baseline CNS BICR, 118 of 279 (combination) and 104 of 278 (monotherapy) randomly assigned patients had ≥one measurable and/or nonmeasurable CNS lesion and were included in the CNS full analysis set (cFAS); 40 of 118 and 38 of 104 had ≥one measurable target CNS lesion and were included in the post hoc CNS evaluable-for-response set (cEFR). In the cFAS, the hazard ratio (HR) for CNS progression or death was 0.58 (95% CI, 0.33 to 1.01). In patients without baseline CNS metastases, the HR for CNS progression or death was 0.67 (95% CI, 0.43 to 1.04). In the cFAS, CNS objective response rates (ORRs; 95% CI) were 73% (combination; 64 to 81) versus 69% (monotherapy; 59 to 78); 59% versus 43% had CNS complete response (CR). In the cEFR, CNS ORRs (95% CI) were 88% (73 to 96) versus 87% (72 to 96); 48% versus 16% had CNS CR.

CONCLUSION:

Osimertinib plus platinum-pemetrexed demonstrated improved CNS efficacy compared with osimertinib monotherapy, including delaying CNS progression, irrespective of baseline CNS metastasis status. These data support this combination as a new first-line treatment for patients with EGFR-mutated advanced NSCLC, including those with CNS metastases.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pirimidinas / Acrilamidas / Neoplasias do Sistema Nervoso Central / Carcinoma Pulmonar de Células não Pequenas / Indóis / Neoplasias Pulmonares Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pirimidinas / Acrilamidas / Neoplasias do Sistema Nervoso Central / Carcinoma Pulmonar de Células não Pequenas / Indóis / Neoplasias Pulmonares Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article