Pralsetinib in patients with RET fusion–positive non-small-cell lung cancer: A plain language summary of the ARROW study

dc.contributor
Institut Català de la Salut
dc.contributor
[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
dc.contributor
Vall d'Hebron Barcelona Hospital Campus
dc.contributor.author
Griesinger, Frank
dc.contributor.author
Baik, Christina
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Tan, Daniel
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Lee, Dae Ho
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Curigliano, Giuseppe
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Subbiah, Vivek
dc.contributor.author
GARRALDA, Elena
dc.date.accessioned
2025-10-25T05:38:39Z
dc.date.available
2025-10-25T05:38:39Z
dc.date.issued
2024-03-12T09:04:52Z
dc.date.issued
2024-03-12T09:04:52Z
dc.date.issued
2024-02
dc.identifier
Griesinger F, Curigliano G, Subbiah V, Baik CS, Tan DS, Lee DH, et al. Pralsetinib in patients with RET fusion–positive non-small cell lung cancer: A plain language summary of the ARROW study. Futur Oncol. 2024 Feb;20(6):297–306.
dc.identifier
1479-6694
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https://hdl.handle.net/11351/11180
dc.identifier
10.2217/fon-2023-0155
dc.identifier
37916501
dc.identifier
001095543700001
dc.identifier.uri
http://hdl.handle.net/11351/11180
dc.description.abstract
RET fusion; Non-small cell lung cancer; Targeted therapy
dc.description.abstract
Fusión RET; Cáncer de pulmón de células no pequeñas; Terapia dirigida
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Fusió RET; Càncer de pulmó de cèl·lules no petites; Teràpia dirigida
dc.description.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)
dc.description.abstract
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.
dc.format
application/pdf
dc.language
eng
dc.publisher
Future Medicine
dc.relation
Future Oncology;20(6)
dc.relation
https://doi.org/10.2217/fon-2023-0155
dc.rights
Attribution-NonCommercial-NoDerivatives 4.0 International
dc.rights
http://creativecommons.org/licenses/by-nc-nd/4.0/
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info:eu-repo/semantics/openAccess
dc.source
Scientia
dc.subject
Pulmons - Càncer - Tractament
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Proteïnes quinases - Inhibidors - Ús terapèutic
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DISEASES::Respiratory Tract Diseases::Lung Diseases::Lung Neoplasms::Carcinoma, Bronchogenic::Respiratory Tract Diseases::Carcinoma, Non-Small-Cell Lung
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Other subheadings::Other subheadings::Other subheadings::/drug therapy
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CHEMICALS AND DRUGS::Enzymes and Coenzymes::Enzymes::Transferases::Phosphotransferases::Phosphotransferases (Alcohol Group Acceptor)::Protein Kinases::Protein-Tyrosine Kinases
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Other subheadings::Other subheadings::Other subheadings::/antagonists & inhibitors
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ENFERMEDADES::enfermedades respiratorias::enfermedades pulmonares::neoplasias pulmonares::carcinoma broncogénico::enfermedades respiratorias::carcinoma de pulmón de células no pequeñas
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Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia
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COMPUESTOS QUÍMICOS Y DROGAS::enzimas y coenzimas::enzimas::transferasas::fosfotransferasas::fosfotransferasas (grupo alcohol aceptor)::proteína cinasas::proteína-tirosina cinasas
dc.subject
Otros calificadores::Otros calificadores::Otros calificadores::/antagonistas & inhibidores
dc.title
Pralsetinib in patients with RET fusion–positive non-small-cell lung cancer: A plain language summary of the ARROW study
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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