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Pralsetinib in patients with RET fusion-positive non-small-cell lung cancer: A plain language summary of the ARROW study.
Griesinger, Frank; Curigliano, Giuseppe; Subbiah, Vivek; Baik, Christina S; Tan, Daniel Sw; Lee, Dae H; Misch, Daniel; Garralda, Elena; Kim, Dong-Wan; van der Wekken, Anthonie J; Gainor, Justin F; Paz-Ares, Luis; Liu, Stephen V; Kalemkerian, Gregory P; Bowles, Daniel W; Mansfield, Aaron S; Lin, Jessica J; Smoljanovic, Vlatka; Rahman, Ahmadur; Zalutskaya, Alena; Louie-Gao, Melinda; Boral, Andy L; Mazières, Julien.
Afiliación
  • Griesinger F; Pius-Hospital, University of Oldenburg, Oldenburg, Germany.
  • Curigliano G; European Institute of Oncology, IRCCS, Milan, Italy.
  • Subbiah V; University of Milano, Milan, Italy.
  • Baik CS; Sarah Cannon Research Institute, Nashville, TN, USA.
  • Tan DS; University of Washington School of Medicine, Seattle, WA, USA.
  • Lee DH; National Cancer Centre Singapore, Singapore.
  • Misch D; Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
  • Garralda E; Helios Clinic Emil von Behring, Berlin, Germany.
  • Kim DW; Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
  • van der Wekken AJ; Seoul National University College of Medicine & Seoul National University Hospital, Seoul, Republic of Korea.
  • Gainor JF; University of Groningen & University Medical Center Groningen, Groningen, Netherlands.
  • Paz-Ares L; Massachusetts General Hospital, Boston, MA, USA.
  • Liu SV; Hospital Universitario 12 de Octubre, Madrid, Spain.
  • Kalemkerian GP; Georgetown University, Washington, DC, USA.
  • Bowles DW; University of Michigan, Ann Arbor, MI, USA.
  • Mansfield AS; University of Colorado School of Medicine, Aurora, CO, USA.
  • Lin JJ; Mayo Clinic, Rochester, NY, USA.
  • Smoljanovic V; Massachusetts General Hospital, Boston, MA, USA.
  • Rahman A; F. Hoffmann-La Roche, Ltd, Basel, Switzerland.
  • Zalutskaya A; F. Hoffmann-La Roche, Ltd, Basel, Switzerland.
  • Louie-Gao M; Blueprint Medicines Corporation, Cambridge, MA, USA.
  • Boral AL; Blueprint Medicines Corporation, Cambridge, MA, USA.
  • Mazières J; Blueprint Medicines Corporation, Cambridge, MA, USA.
Future Oncol ; 20(6): 297-306, 2024 Feb.
Article en En | MEDLINE | ID: mdl-37916501
ABSTRACT
WHAT IS THIS SUMMARY ABOUT? This is a summary of a research study called ARROW, which tested a medicine called pralsetinib in patients with non-small cell lung cancer (NSCLC), thyroid cancer, and other advanced solid tumours caused by a change in a gene called RET. For the purposes of this summary, only patients with NSCLC with a change in RET called fusion (RET fusion+) are highlighted. WHAT WERE THE RESULTS? In total, 281 patients with RET fusion+ NSCLC had taken part in this study across the USA, Europe, and Asia. Patients were asked to take four pills (adding up to 400 mg) of pralsetinib each day and were checked for any changes in their tumours, as well as for any side effects. After an average of 8 months of treatment with pralsetinib, 72% of previously untreated patients and 59% of patients who had previously received chemotherapy had considerable shrinkage of their tumours. Among 10 patients with tumours which had spread to the brain (all of whom had received previous treatments), 70% had their tumours shrink greatly in the brain after treatment with pralsetinib. On average, patients lived with little to no tumour growth for 16 months. In previously untreated patients, the most common severe side effects that were considered related to pralsetinib treatment were decreased white blood cells (neutrophils and lymphocytes), increased blood pressure, and an increase in a blood protein called creatine phosphokinase. In previously treated patients, the severe side effects were decreased white blood cells (neutrophils, lymphocytes, and leukocytes), increased blood pressure, and low levels of red blood cells. In both untreated and previously treated patients, the most common severe side effects that required hospital attention were lung inflammation/swelling causing shortness of breath (pneumonitis) and lung infection (pneumonia). WHAT DO THE RESULTS MEAN? Overall, the ARROW study showed that pralsetinib was effective in shrinking tumours in patients with RET fusion+ NSCLC regardless of previous treatment history. The recorded side effects were expected in patients receiving this type of medicine. Clinical Trial Registration NCT03037385 (ARROW) (ClinicalTrials.gov).
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pirimidinas / Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Límite: Humans Idioma: En Revista: Future Oncol Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pirimidinas / Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Límite: Humans Idioma: En Revista: Future Oncol Año: 2024 Tipo del documento: Article País de afiliación: Alemania