Institut Català de la Salut
[Griesinger F] Pius-Hospital, University of Oldenburg, Oldenburg, Germany. [Curigliano G] European Institute of Oncology, IRCCS, Milan, Italy. University of Milano, Milan, Italy. [Subbiah V] Sarah Cannon Research Institute, Nashville, TN, USA. [Baik CS] University of Washington School of Medicine, Seattle, WA, USA. [Tan DSW] National Cancer Centre Singapore, Singapore. [Lee DH] Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea. [Garralda E] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
Vall d'Hebron Barcelona Hospital Campus
2024-03-12T09:04:52Z
2024-03-12T09:04:52Z
2024-02
RET fusion; Non-small cell lung cancer; Targeted therapy
Fusión RET; Cáncer de pulmón de células no pequeñas; Terapia dirigida
Fusió RET; Càncer de pulmó de cèl·lules no petites; Teràpia dirigida
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)
Medical writing support, including assisting authors with the development of the outline and initial draft as well as incorporation of comments was provided by Kyle Wiid, MSc, and editorial support, including proofreading, and submission was provided by Agata Shodeke, PhD, all of Paragon, Knutsford, funded by Blueprint Medicines Corporation and F. Hoffmann-La Roche, Ltd, according to Good Publication Practice guidelines. The sponsor was involved in the study design and collection, analysis and interpretation of data, as well as data checking of information provided in the manuscript.
Article
Published version
English
Pulmons - Càncer - Tractament; Proteïnes quinases - Inhibidors - Ús terapèutic; DISEASES::Respiratory Tract Diseases::Lung Diseases::Lung Neoplasms::Carcinoma, Bronchogenic::Respiratory Tract Diseases::Carcinoma, Non-Small-Cell Lung; Other subheadings::Other subheadings::Other subheadings::/drug therapy; CHEMICALS AND DRUGS::Enzymes and Coenzymes::Enzymes::Transferases::Phosphotransferases::Phosphotransferases (Alcohol Group Acceptor)::Protein Kinases::Protein-Tyrosine Kinases; Other subheadings::Other subheadings::Other subheadings::/antagonists & inhibitors; ENFERMEDADES::enfermedades respiratorias::enfermedades pulmonares::neoplasias pulmonares::carcinoma broncogénico::enfermedades respiratorias::carcinoma de pulmón de células no pequeñas; Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia; COMPUESTOS QUÍMICOS Y DROGAS::enzimas y coenzimas::enzimas::transferasas::fosfotransferasas::fosfotransferasas (grupo alcohol aceptor)::proteína cinasas::proteína-tirosina cinasas; Otros calificadores::Otros calificadores::Otros calificadores::/antagonistas & inhibidores
Future Medicine
Future Oncology;20(6)
https://doi.org/10.2217/fon-2023-0155
Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/