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Exceptional response to alectinib for duodenal carcinoma with ALK fusion: A case report and literature review.
Isaka, Yuri; Sasaki, Akinori; Saito, Akira; Motomura, Yasuaki; Ando, Yayoi; Nakamura, Yoshiaki.
Afiliação
  • Isaka Y; Department of Gastroenterology, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, Japan.
  • Sasaki A; Department of Gastroenterology, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, Japan.
  • Saito A; Department of Pathology, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, Japan.
  • Motomura Y; Department of Gastroenterology, Tokyo Bay Urayasu Ichikawa Medical Center, Urayasu, Japan.
  • Ando Y; Clinical Research Support Office, National Cancer Center Hospital Chuou, Tokyo, Japan.
  • Nakamura Y; Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Front Oncol ; 12: 1064944, 2022.
Article em En | MEDLINE | ID: mdl-36713517
ABSTRACT
Patients with advanced duodenal carcinoma usually have a poor prognosis due to limited effective chemotherapy options. The study for genotype-directed therapy in patients with duodenal carcinoma is progressing. However, no clinical data assessing the efficacy of molecularly targeted therapy are presently available. We report the case of a 64-year-old woman who was diagnosed with anaplastic lymphocyte kinase (ALK) fusion-positive advanced duodenal carcinoma. Echinoderm microtubule associated protein like-4 (EML4)-ALK rearrangement was detected by comprehensive genomic profiling after resistance to first-line chemotherapy. The patient received alectinib, an ALK inhibitor, with marked shrinkage in primary tumor and liver metastases. She is currently being treated with alectinib for 6 months or more. This is the first report of the efficacy of alectinib in a patient with duodenal carcinoma harboring ALK fusion. Additionally, this case report suggests that the practical use of next-generation sequencing may expand optimal treatment choices in rare solid tumors, including duodenal carcinoma.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article