Expert consensus on the management of adverse events of Lorlatinib in the treatment of ALK+ advanced non-small cell lung cancer

dc.contributor.authorArriola Aperribay, Edurne
dc.contributor.authorCastro, Javier de
dc.contributor.authorGarcía Campelo, Rosario
dc.contributor.authorBernárdez, Beatriz
dc.contributor.authorBernabé, Reyes
dc.contributor.authorBruna, Jordi
dc.contributor.authorDómine, Manuel
dc.contributor.authorIsla, Dolores
dc.contributor.authorJuan Vidal, Óscar
dc.contributor.authorLópez Fernández, Teresa
dc.contributor.authorNadal, Ernest
dc.contributor.authorRodríguez Abreu, Delvys
dc.contributor.authorVares, María
dc.contributor.authorAsensio, Úrsula
dc.contributor.authorGarcía, Luis F.
dc.contributor.authorFelip, Enriqueta
dc.date.accessioned2025-09-01T07:33:23Z
dc.date.available2025-09-01T07:33:23Z
dc.date.issued2024-07-31
dc.date.updated2025-08-29T13:47:56Z
dc.description.abstractThe use of anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitors (TKIs), such as lorlatinib, for the treatment of patients with ALK gene rearrangement (or ALK-positive) non-small cell lung cancer (NSCLC) has been shown to improve the overall survival and quality of life of these patients. However, lorlatinib is not exempt from potential adverse events. Adequate monitoring and management of these adverse events are critical for increasing patient adherence to lorlatinib, thereby maximizing the benefits of treatment and minimizing the risks associated with treatment discontinuation. Considering that the adverse events of lorlatinib can affect different organs and systems, the participation of a multidisciplinary team, including cardiologists, neurologists, internal medicine specialists, and oncology pharmacists, is needed. This article presents specific and pragmatic strategies for identifying and treating the most relevant adverse events associated with lorlatinib in patients with advanced ALK-positive NSCLC based on the clinical experience of a multidisciplinary panel of experts.
dc.format.extent24 p.
dc.format.mimetypeapplication/pdf
dc.identifier.issn1179-1918
dc.identifier.pmid39085682
dc.identifier.urihttps://hdl.handle.net/2445/222864
dc.language.isoeng
dc.publisherSpringer Science and Business Media LLC
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1007/s40261-024-01379-7
dc.relation.ispartofClinical Drug Investigation, 2024, vol. 44, num. 8, p. 553-576
dc.relation.urihttps://doi.org/10.1007/s40261-024-01379-7
dc.rightscc-by-nc (c) Arriola Aperribay, Edurne et al., 2024
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationMedicaments antineoplàstics
dc.subject.classificationCàncer de pulmó
dc.subject.otherAntineoplastic agents
dc.subject.otherLung cancer
dc.titleExpert consensus on the management of adverse events of Lorlatinib in the treatment of ALK+ advanced non-small cell lung cancer
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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