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High-Dose Osimertinib for CNS Progression in EGFR+ NSCLC: A Multi-Institutional Experience.
Piper-Vallillo, A J; Rotow, Julia K; Aredo, Jacqueline V; Shaverdashvili, Khvaramze; Luo, Jia; Carlisle, Jennifer W; Husain, Hatim; Muzikansky, Alona; Heist, Rebecca S; Rangachari, Deepa; Ramalingam, Suresh S; Wakelee, Heather A; Yu, Helena A; Sequist, Lecia V; Bauml, Joshua M; Neal, Joel W; Piotrowska, Zofia.
Afiliação
  • Piper-Vallillo AJ; Massachusetts General Hospital, Boston, Massachusetts.
  • Rotow JK; Beth Israel Deaconess Medical Center, Boston, Massachusetts.
  • Aredo JV; Harvard Medical School, Boston, Massachusetts.
  • Shaverdashvili K; Dana Farber Cancer Institute, Boston, Massachusetts.
  • Luo J; Stanford University School of Medicine, Stanford, California.
  • Carlisle JW; Abramson Cancer Center at the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Husain H; Harvard Medical School, Boston, Massachusetts.
  • Muzikansky A; Dana Farber Cancer Institute, Boston, Massachusetts.
  • Heist RS; Memorial Sloan Kettering Cancer Center, New York, New York.
  • Rangachari D; Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia.
  • Ramalingam SS; University of California San Diego Medical Center, La Jolla, California.
  • Wakelee HA; Massachusetts General Hospital, Boston, Massachusetts.
  • Yu HA; Massachusetts General Hospital, Boston, Massachusetts.
  • Sequist LV; Harvard Medical School, Boston, Massachusetts.
  • Bauml JM; Beth Israel Deaconess Medical Center, Boston, Massachusetts.
  • Neal JW; Harvard Medical School, Boston, Massachusetts.
  • Piotrowska Z; Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia.
JTO Clin Res Rep ; 3(6): 100328, 2022 Jun.
Article em En | MEDLINE | ID: mdl-35637759
Introduction: This multicenter review evaluated the efficacy and safety of osimertinib dose escalation for central nervous system (CNS) progression developing on osimertinib 80 mg in EGFR-mutant NSCLC. Methods: Retrospective review identified 105 patients from eight institutions with advanced EGFR-mutant NSCLC treated with osimertinib 160 mg daily between October 2013 and January 2020. Radiographic responses were clinically assessed, and Kaplan-Meier analyses were used. We defined CNS disease control as the interval from osimertinib 160 mg initiation to CNS progression or discontinuation of osimertinib 160 mg. Results: Among 105 patients treated with osimertinib 160 mg, 69 were escalated for CNS progression, including 24 treated with dose escalation alone (cohort A), 34 who received dose-escalated osimertinib plus concurrent chemotherapy and/or radiation (cohort B), and 11 who received osimertinib 160 mg without any prior 80 mg exposure. The median duration of CNS control was 3.8 months (95% confidence interval [CI], 1.7-5.8) in cohort A, 5.1 months (95% CI, 3.1-6.5) in cohort B, and 4.2 months (95% CI 1.6-not reached) in cohort C. Across all cohorts, the median duration of CNS control was 6.0 months (95% CI, 5.1-9.0) in isolated leptomeningeal progression (n = 27) and 3.3 months (95% CI, 1.0-3.1) among those with parenchymal-only metastases (n = 23). Patients on osimertinib 160 mg experienced no severe or unexpected side effects. Conclusion: Among patients with EGFR-mutant NSCLC experiencing CNS progression on osimertinib 80 mg daily, dose escalation to 160 mg provided modest benefit with CNS control lasting approximately 3 to 6 months and seemed more effective in patients with isolated leptomeningeal CNS progression.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JTO Clin Res Rep Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JTO Clin Res Rep Ano de publicação: 2022 Tipo de documento: Article