Advances in RAS therapeutics for pancreatic cancer

Por: Der, Channing J [Autor]Colaborador(es): Yeh, Jen JenTipo de material: TextoTextoIdioma: Inglés Descripción: páginas: 1857-1861Tema(s): CÁNCER | CÁNCER DEL TRACTO GASTROINTESTINAL | GASTROENTEROLOGÍA | HEMATOLOGÍA | ONCOLOGÍA | GENÉTICA GENERAL En: The New England Journal of MedicineResumen: Somatic mutations in the Kirsten rat sarcoma viral oncogene homologue (KRAS) occur in more than 90% of pancreatic ductal adenocarcinomas. In this issue of the Journal, Wolpin et al. evaluated the side-effect profile of and response to a first-in-class small-molecule drug called daraxonrasib, which targets the active state of RAS (see Key Concepts) in patients with metastatic pancreatic ductal adenocarcinoma who have received at least one previous line of chemotherapy. In the context of second-line treatment, they reported an objective response according to the Response Evaluation Criteria in Solid Tumors (RECIST), version 1.1, in up to 35% of patients and a median response duration of 8.2 months.
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Colección General NEJM (Navegar estantería) Vol.394, No.18 (2026) Disponible NEJM015

Somatic mutations in the Kirsten rat sarcoma viral oncogene homologue (KRAS) occur in more than 90% of pancreatic ductal adenocarcinomas. In this issue of the Journal, Wolpin et al. evaluated the side-effect profile of and response to a first-in-class small-molecule drug called daraxonrasib, which targets the active state of RAS (see Key Concepts) in patients with metastatic pancreatic ductal adenocarcinoma who have received at least one previous line of chemotherapy. In the context of second-line treatment, they reported an objective response according to the Response Evaluation Criteria in Solid Tumors (RECIST), version 1.1, in up to 35% of patients and a median response duration of 8.2 months.