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Characterization and Management of Hedgehog Pathway Inhibitor-Related Adverse Events in Patients With Advanced Basal Cell Carcinoma

Abnormal activation of hedgehog pathway signaling is a key driver in the pathogenesis of basal cell carcinoma (BCC). Vismodegib, a first-in-class small-molecule inhibitor of hedgehog pathway signaling, is approved by regulatory authorities for the treatment of adults who have metastatic BCC or local...

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Autores principales: Lacouture, Mario E., Dréno, Brigitte, Ascierto, Paolo Antonio, Dummer, Reinhard, Basset-Seguin, Nicole, Fife, Kate, Ernst, Scott, Licitra, Lisa, Neves, Rogerio I., Peris, Ketty, Puig, Susana, Sokolof, Jonas, Sekulic, Aleksandar, Hauschild, Axel, Kunstfeld, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AlphaMed Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061532/
https://www.ncbi.nlm.nih.gov/pubmed/27511905
http://dx.doi.org/10.1634/theoncologist.2016-0186
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author Lacouture, Mario E.
Dréno, Brigitte
Ascierto, Paolo Antonio
Dummer, Reinhard
Basset-Seguin, Nicole
Fife, Kate
Ernst, Scott
Licitra, Lisa
Neves, Rogerio I.
Peris, Ketty
Puig, Susana
Sokolof, Jonas
Sekulic, Aleksandar
Hauschild, Axel
Kunstfeld, Rainer
author_facet Lacouture, Mario E.
Dréno, Brigitte
Ascierto, Paolo Antonio
Dummer, Reinhard
Basset-Seguin, Nicole
Fife, Kate
Ernst, Scott
Licitra, Lisa
Neves, Rogerio I.
Peris, Ketty
Puig, Susana
Sokolof, Jonas
Sekulic, Aleksandar
Hauschild, Axel
Kunstfeld, Rainer
author_sort Lacouture, Mario E.
collection PubMed
description Abnormal activation of hedgehog pathway signaling is a key driver in the pathogenesis of basal cell carcinoma (BCC). Vismodegib, a first-in-class small-molecule inhibitor of hedgehog pathway signaling, is approved by regulatory authorities for the treatment of adults who have metastatic BCC or locally advanced BCC that has recurred after surgery, or who are not candidates for surgery and who are not candidates for radiation. A second inhibitor, sonidegib, was also recently approved for the same patient group with locally advanced BCC. Adverse events (AEs) commonly observed in hedgehog pathway inhibitor (HPI)-treated patients include muscle spasms, ageusia/dysgeusia, alopecia, weight loss, and asthenia (fatigue). These AEs are thought to be mechanistically related to inhibition of the hedgehog pathway in normal tissue. Although the severity of the majority of AEs associated with HPIs is grade 1–2, the long-term nature of these AEs can lead to decreased quality of life, treatment interruption, and in some cases discontinuation, all of which might affect clinical outcome. The incidence, clinical presentation, putative mechanisms, and management strategies for AEs related to HPIs in advanced BCC are described. These observations represent the first step toward the development of mechanism-based preventive and management strategies. Knowledge of these AEs will allow health care professionals to provide appropriate counseling and supportive care interventions, all of which will contribute to improved quality of life and optimal benefit from therapy. IMPLICATIONS FOR PRACTICE: The hedgehog pathway inhibitors (HPIs) vismodegib and sonidegib represent a therapeutic breakthrough for patients with advanced basal cell carcinoma. However, the nature of the low-grade adverse events (AEs) commonly observed in HPI-treated patients, including muscle spasms, ageusia/dysgeusia, alopecia, weight loss, and fatigue, can impact clinical outcomes as a result of decreased quality of life and treatment discontinuation. The incidence, clinical presentation, putative mechanisms, and management strategies for AEs related to administration of HPIs are described, with the goal of enabling health care professionals to provide appropriate counseling and supportive care interventions to their patients.
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spelling pubmed-50615322017-04-01 Characterization and Management of Hedgehog Pathway Inhibitor-Related Adverse Events in Patients With Advanced Basal Cell Carcinoma Lacouture, Mario E. Dréno, Brigitte Ascierto, Paolo Antonio Dummer, Reinhard Basset-Seguin, Nicole Fife, Kate Ernst, Scott Licitra, Lisa Neves, Rogerio I. Peris, Ketty Puig, Susana Sokolof, Jonas Sekulic, Aleksandar Hauschild, Axel Kunstfeld, Rainer Oncologist Melanoma and Cutaneous Malignancies Abnormal activation of hedgehog pathway signaling is a key driver in the pathogenesis of basal cell carcinoma (BCC). Vismodegib, a first-in-class small-molecule inhibitor of hedgehog pathway signaling, is approved by regulatory authorities for the treatment of adults who have metastatic BCC or locally advanced BCC that has recurred after surgery, or who are not candidates for surgery and who are not candidates for radiation. A second inhibitor, sonidegib, was also recently approved for the same patient group with locally advanced BCC. Adverse events (AEs) commonly observed in hedgehog pathway inhibitor (HPI)-treated patients include muscle spasms, ageusia/dysgeusia, alopecia, weight loss, and asthenia (fatigue). These AEs are thought to be mechanistically related to inhibition of the hedgehog pathway in normal tissue. Although the severity of the majority of AEs associated with HPIs is grade 1–2, the long-term nature of these AEs can lead to decreased quality of life, treatment interruption, and in some cases discontinuation, all of which might affect clinical outcome. The incidence, clinical presentation, putative mechanisms, and management strategies for AEs related to HPIs in advanced BCC are described. These observations represent the first step toward the development of mechanism-based preventive and management strategies. Knowledge of these AEs will allow health care professionals to provide appropriate counseling and supportive care interventions, all of which will contribute to improved quality of life and optimal benefit from therapy. IMPLICATIONS FOR PRACTICE: The hedgehog pathway inhibitors (HPIs) vismodegib and sonidegib represent a therapeutic breakthrough for patients with advanced basal cell carcinoma. However, the nature of the low-grade adverse events (AEs) commonly observed in HPI-treated patients, including muscle spasms, ageusia/dysgeusia, alopecia, weight loss, and fatigue, can impact clinical outcomes as a result of decreased quality of life and treatment discontinuation. The incidence, clinical presentation, putative mechanisms, and management strategies for AEs related to administration of HPIs are described, with the goal of enabling health care professionals to provide appropriate counseling and supportive care interventions to their patients. AlphaMed Press 2016-10 2016-08-10 /pmc/articles/PMC5061532/ /pubmed/27511905 http://dx.doi.org/10.1634/theoncologist.2016-0186 Text en ©AlphaMed Press
spellingShingle Melanoma and Cutaneous Malignancies
Lacouture, Mario E.
Dréno, Brigitte
Ascierto, Paolo Antonio
Dummer, Reinhard
Basset-Seguin, Nicole
Fife, Kate
Ernst, Scott
Licitra, Lisa
Neves, Rogerio I.
Peris, Ketty
Puig, Susana
Sokolof, Jonas
Sekulic, Aleksandar
Hauschild, Axel
Kunstfeld, Rainer
Characterization and Management of Hedgehog Pathway Inhibitor-Related Adverse Events in Patients With Advanced Basal Cell Carcinoma
title Characterization and Management of Hedgehog Pathway Inhibitor-Related Adverse Events in Patients With Advanced Basal Cell Carcinoma
title_full Characterization and Management of Hedgehog Pathway Inhibitor-Related Adverse Events in Patients With Advanced Basal Cell Carcinoma
title_fullStr Characterization and Management of Hedgehog Pathway Inhibitor-Related Adverse Events in Patients With Advanced Basal Cell Carcinoma
title_full_unstemmed Characterization and Management of Hedgehog Pathway Inhibitor-Related Adverse Events in Patients With Advanced Basal Cell Carcinoma
title_short Characterization and Management of Hedgehog Pathway Inhibitor-Related Adverse Events in Patients With Advanced Basal Cell Carcinoma
title_sort characterization and management of hedgehog pathway inhibitor-related adverse events in patients with advanced basal cell carcinoma
topic Melanoma and Cutaneous Malignancies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061532/
https://www.ncbi.nlm.nih.gov/pubmed/27511905
http://dx.doi.org/10.1634/theoncologist.2016-0186
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