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

Author:

Lacouture Mario E.1,Dréno Brigitte2,Ascierto Paolo Antonio3,Dummer Reinhard4,Basset-Seguin Nicole5,Fife Kate6,Ernst Scott7,Licitra Lisa8,Neves Rogerio I.9,Peris Ketty10,Puig Susana11,Sokolof Jonas1,Sekulic Aleksandar12,Hauschild Axel13,Kunstfeld Rainer14

Affiliation:

1. Memorial Sloan Kettering Cancer Center, New York, New York, USA

2. Department of Dermatology, Hôtel Dieu University Hospital, Nantes, France

3. Istituto Nazionale Tumori Fondazione, G Pascale, Naples, Italy

4. University of Zurich Hospital, Zurich, Switzerland

5. Université Paris 7 and Hôpital Saint-Louis, Paris, France

6. Cambridge University Hospitals National Health Service Foundation Trust, Cambridge, United Kingdom

7. Western University London Regional Cancer Program, London, Ontario, Canada

8. Fondazione IRCCS, Istituto Tumori, Milan, Italy

9. Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA

10. Catholic University of Rome, Rome, Italy

11. Dermatology Department, Hospital Clinic, University of Barcelona, Institut d’Investigacions Biomédiques August Pi I Sunyer, Barcelona, Spain

12. Mayo Clinic, Scottsdale, Arizona, USA

13. Department of Dermatology, University of Kiel, Kiel, Germany

14. Medical University of Vienna, Vienna, Austria

Abstract

Abstract 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.

Funder

F. Hoffmann-La Roche, Ltd

Neither F. Hoffman-La Roche, Ltd.

National Institutes of Health

National Cancer Institute Cancer Center

Spanish Fondo de Investigaciones Sanitarias

CIBER de Enfermedades Raras of the Instituto de Salud Carlos III

AGAUR

SGR

European Commission under the 6th Framework Programme

European Commission under the 7th Framework Programme

National Cancer Institute

U.S. National Institute of Health

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

Reference79 articles.

1. Profile of vismodegib and its potential in the treatment of advanced basal cell carcinoma;Macha;Cancer Manag Res,2013

2. Advanced basal cell carcinoma of the skin: Targeting the hedgehog pathway;Sekulic;Curr Opin Oncol,2013

3. Treatment with two different doses of sonidegib in patients with locally advanced or metastatic basal cell carcinoma (BOLT): A multicentre, randomised, double-blind phase 2 trial;Migden;Lancet Oncol,2015

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