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Adagrasib Treatment After Sotorasib-Related Hepatotoxicity in Patients With KRASG12C-Mutated Non-Small Cell Lung Cancer: A Case Series and Literature Review.
Luo, Jia; Florez, Narjust; Donnelly, Anjali; Lou, Yanyan; Lu, Kevin; Ma, Patrick C; Spira, Alexander I; Ryan, Debra; Husain, Hatim.
Afiliação
  • Luo J; Dana-Farber Cancer Institute, Boston, MA.
  • Florez N; Brigham and Women's Hospital, Boston, MA.
  • Donnelly A; Harvard Medical School, Boston, MA.
  • Lou Y; Dana-Farber Cancer Institute, Boston, MA.
  • Lu K; Brigham and Women's Hospital, Boston, MA.
  • Ma PC; Harvard Medical School, Boston, MA.
  • Spira AI; University of Michigan, Ann Arbor, MI.
  • Ryan D; Virginia Cancer Specialists, Fairfax, VA.
  • Husain H; Mayo Clinic, Jacksonville, FL.
JCO Precis Oncol ; 8: e2300644, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38579193
ABSTRACT

PURPOSE:

KRAS is the most commonly mutated driver oncogene in non-small cell lung cancer (NSCLC). Sotorasib and adagrasib, KRASG12C inhibitors, have been granted accelerated US approval; however, hepatotoxicity is a common side effect with higher rates in patients treated with sotorasib proximal to checkpoint inhibitor (CPI) therapy. The aim of this study was to assess the feasibility and safety of adagrasib after discontinuation of sotorasib because of treatment-related grade 3 hepatotoxicity through real-world and clinical cases.

METHODS:

Medical records from five patients treated in real-world settings were retrospectively reviewed. Patients had locally advanced or metastatic KRASG12C-mutated NSCLC and received adagrasib after sotorasib in the absence of extracranial disease progression. Additional data were collected for 12 patients with KRASG12C-mutated NSCLC enrolled in a phase Ib cohort of the KRYSTAL-1 study and previously treated with sotorasib. The end points associated with both drugs included timing and severity of hepatotoxicity, best overall response, and duration of therapy.

RESULTS:

All patients were treated with CPIs followed by sotorasib (initiated 0-64 days after CPI). All five real-world patients experienced hepatotoxicity with sotorasib that led to treatment discontinuation, whereas none experienced treatment-related hepatotoxicity with subsequent adagrasib treatment. Three patients from KRYSTAL-1 transitioned from sotorasib to adagrasib because of hepatotoxicity; one experienced grade 3 ALT elevation on adagrasib that resolved with therapy interruption and dose reduction.

CONCLUSION:

Adagrasib may have a distinct hepatotoxicity profile from sotorasib and is more easily combined with CPIs either sequentially or concurrently. These differences may be used to inform clinical decisions regarding an initial KRASG12C inhibitor for patients who recently discontinued a CPI or experience hepatotoxicity on sotorasib.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Acetonitrilas / Piperazinas / Piridinas / Pirimidinas / Carcinoma Pulmonar de Células não Pequenas / Doença Hepática Induzida por Substâncias e Drogas / Neoplasias Pulmonares Limite: Humans Idioma: En Revista: JCO Precis Oncol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Acetonitrilas / Piperazinas / Piridinas / Pirimidinas / Carcinoma Pulmonar de Células não Pequenas / Doença Hepática Induzida por Substâncias e Drogas / Neoplasias Pulmonares Limite: Humans Idioma: En Revista: JCO Precis Oncol Ano de publicação: 2024 Tipo de documento: Article