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Characterization and management of adverse events observed with mobocertinib (TAK-788) treatment for EGFR exon 20 insertion-positive non-small cell lung cancer.
Yang, James Chih-Hsin; Zhou, Caicun; Jänne, Pasi A; Ramalingam, Suresh S; Kim, Tae Min; Riely, Gregory J; Spira, Alexander I; Piotrowska, Zofia; Mekhail, Tarek; Garcia Campelo, Maria Rosario; Felip, Enriqueta; Bazhenova, Lyudmila; Jin, Shu; Kaur, Manmit; Diderichsen, Paul M; Gupta, Neeraj; Bunn, Veronica; Lin, Jianchang; N Churchill, Eric; Mehta, Minal; Nguyen, Danny.
Afiliación
  • Yang JC; Graduate Institute of Oncology, National Taiwan University Hospital and National Taiwan University Cancer Center, Taipei, Taiwan.
  • Zhou C; Shanghai Pulmonary Hospital, Shanghai, China.
  • Jänne PA; Dana-Farber Cancer Institute, Boston, MA, USA.
  • Ramalingam SS; School of Medicine, Emory University, Atlanta, GA, USA.
  • Kim TM; Seoul National University Hospital, Seoul, South Korea.
  • Riely GJ; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Spira AI; Medical Oncology, Virginia Cancer Specialists and US Oncology Research, Fairfax, VA, USA.
  • Piotrowska Z; Massachusetts General Hospital Cancer Center, Boston, MA, USA.
  • Mekhail T; Thoracic Cancer Program, AdventHealth Orlando, Orlando, FL, USA.
  • Garcia Campelo MR; Medical Oncology Department, Thoracic Tumors Unit, University Hospital A Coruña, CHUAC, A Coruña, Spain.
  • Felip E; Vall d'Hebron University Hospital, Barcelona, Spain.
  • Bazhenova L; University of California San Diego Moores Cancer Center, La Jolla, CA, USA.
  • Jin S; Clinical Science, Oncology, Takeda Development Center Americas, Inc., Lexington, MA, USA.
  • Kaur M; Takeda Pharmaceuticals U.S.A., Inc, Lexington, MA, USA.
  • Diderichsen PM; o Integrated Drug Development, Certara, Princeton, NJ, USA.
  • Gupta N; Quantitative Clinical Pharmacology, Takeda Development Center Americas, Inc., Lexington, MA, USA.
  • Bunn V; Medical Safety Oncology, Takeda Development Center Americas, Inc., Lexington, MA, USA.
  • Lin J; City of Hope National Medical Center, USA.
  • N Churchill E; Oncology Statistics, Takeda Development Center Americas, Inc., Lexington, MA, USA.
  • Mehta M; City of Hope National Medical Center, USA.
  • Nguyen D; Global Medical Affairs Oncology, Takeda Pharmaceuticals U.S.A., Inc., Lexington, MA, USA.
Expert Rev Anticancer Ther ; 23(1): 95-106, 2023 Jan.
Article en En | MEDLINE | ID: mdl-36537204
Mobocertinib is a treatment for patients with a certain type of lung cancer. We analyzed the safety of mobocertinib in 257 patients with lung cancer. The most common side effects with mobocertinib were diarrhea, nausea, vomiting, and skin rash. In 114 patients with lung cancer who were treated in the past with chemotherapy that included platinum-based drugs, diarrhea started after about 5 days of mobocertinib treatment and went away in about 2 days. Skin-related side effects started after about 9 days and went away in about 2.5 months. One-fifth of patients who had to receive a smaller amount of mobocertinib because of side effects responded to treatment compared with one-third of patients who received the recommended mobocertinib amount. Managing side effects quickly can better help patients with lung cancer who are treated with mobocertinib.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Límite: Humans Idioma: En Revista: Expert Rev Anticancer Ther Asunto de la revista: NEOPLASIAS / TERAPEUTICA Año: 2023 Tipo del documento: Article País de afiliación: Taiwán

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Límite: Humans Idioma: En Revista: Expert Rev Anticancer Ther Asunto de la revista: NEOPLASIAS / TERAPEUTICA Año: 2023 Tipo del documento: Article País de afiliación: Taiwán