Cargando…

Long‐term efficacy and safety of sonidegib in patients with advanced basal cell carcinoma: 42‐month analysis of the phase II randomized, double‐blind BOLT study

BACKGROUND: Basal cell carcinomas (BCCs) exhibit aberrant activation of the hedgehog pathway. Sonidegib is a hedgehog pathway inhibitor approved for the treatment of locally advanced BCC (laBCC) and metastatic BCC (mBCC) based on primary results of the BOLT study [Basal Cell Carcinoma Outcomes with...

Descripción completa

Detalles Bibliográficos
Autores principales: Dummer, R., Guminksi, A., Gutzmer, R., Lear, J.T., Lewis, K.D., Chang, A.L.S., Combemale, P., Dirix, L., Kaatz, M., Kudchadkar, R., Loquai, C., Plummer, R., Schulze, H.‐J., Stratigos, A.J., Trefzer, U., Squittieri, N., Migden, M.R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318253/
https://www.ncbi.nlm.nih.gov/pubmed/31545507
http://dx.doi.org/10.1111/bjd.18552
_version_ 1783550804504870912
author Dummer, R.
Guminksi, A.
Gutzmer, R.
Lear, J.T.
Lewis, K.D.
Chang, A.L.S.
Combemale, P.
Dirix, L.
Kaatz, M.
Kudchadkar, R.
Loquai, C.
Plummer, R.
Schulze, H.‐J.
Stratigos, A.J.
Trefzer, U.
Squittieri, N.
Migden, M.R.
author_facet Dummer, R.
Guminksi, A.
Gutzmer, R.
Lear, J.T.
Lewis, K.D.
Chang, A.L.S.
Combemale, P.
Dirix, L.
Kaatz, M.
Kudchadkar, R.
Loquai, C.
Plummer, R.
Schulze, H.‐J.
Stratigos, A.J.
Trefzer, U.
Squittieri, N.
Migden, M.R.
author_sort Dummer, R.
collection PubMed
description BACKGROUND: Basal cell carcinomas (BCCs) exhibit aberrant activation of the hedgehog pathway. Sonidegib is a hedgehog pathway inhibitor approved for the treatment of locally advanced BCC (laBCC) and metastatic BCC (mBCC) based on primary results of the BOLT study [Basal Cell Carcinoma Outcomes with LDE225 (sonidegib) Treatment]. OBJECTIVES: This is the final 42‐month analysis of the BOLT study, evaluating the efficacy and safety of sonidegib. METHODS: Adults with no prior hedgehog pathway inhibitor therapy were randomized in a 1 : 2 ratio to sonidegib 200 mg or 800 mg once daily. Treatment continued for up to 42 months or until disease progression, unacceptable toxicity, death, study termination or withdrawal of consent. The primary efficacy end point was the objective response rate (ORR) by central review, assessed at baseline; weeks 5, 9 and 17; then subsequently every 8 or 12 weeks during years 1 or 2, respectively. Safety end points included adverse event monitoring and reporting. RESULTS: The study enrolled 230 patients, 79 and 151 in the 200‐mg and 800‐mg groups, respectively, of whom 8% and 3.3% remained on treatment by the 42‐month cutoff, respectively. The ORRs by central review were 56% [95% confidence interval (CI) 43–68] for laBCC and 8% (95% CI 0·2–36) for mBCC in the 200‐mg group and 46·1% (95% CI 37·2–55·1) for laBCC and 17% (95% CI 5–39) for mBCC in the 800‐mg group. No new safety concerns emerged. CONCLUSIONS: Sonidegib demonstrated sustained efficacy and a manageable safety profile. The final BOLT results support sonidegib as a viable treatment option for laBCC and mBCC. What's already known about this topic? Basal cell carcinoma (BCC) is usually treatable with surgery or radiation therapy, but there are limited treatment options for patients with advanced BCC. Sonidegib, a hedgehog pathway inhibitor approved for the treatment of advanced BCC, demonstrated clinically relevant efficacy and manageable safety in prior analyses of the phase II randomized, double‐blind BOLT study [Basal Cell Carcinoma Outcomes with LDE225 (sonidegib) Treatment]. What does this study add? This final 42‐month analysis of BOLT is the longest follow‐up available for a hedgehog pathway inhibitor. Clinically relevant efficacy results were sustained from prior analyses, with objective response rates by central review of the approved 200‐mg daily dose of 56% in locally advanced BCC and 8% in metastatic BCC. No new safety concerns were raised. The results confirmed sonidegib as a viable long‐term treatment option for patients with advanced BCC.
format Online
Article
Text
id pubmed-7318253
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-73182532020-06-29 Long‐term efficacy and safety of sonidegib in patients with advanced basal cell carcinoma: 42‐month analysis of the phase II randomized, double‐blind BOLT study Dummer, R. Guminksi, A. Gutzmer, R. Lear, J.T. Lewis, K.D. Chang, A.L.S. Combemale, P. Dirix, L. Kaatz, M. Kudchadkar, R. Loquai, C. Plummer, R. Schulze, H.‐J. Stratigos, A.J. Trefzer, U. Squittieri, N. Migden, M.R. Br J Dermatol Original Articles BACKGROUND: Basal cell carcinomas (BCCs) exhibit aberrant activation of the hedgehog pathway. Sonidegib is a hedgehog pathway inhibitor approved for the treatment of locally advanced BCC (laBCC) and metastatic BCC (mBCC) based on primary results of the BOLT study [Basal Cell Carcinoma Outcomes with LDE225 (sonidegib) Treatment]. OBJECTIVES: This is the final 42‐month analysis of the BOLT study, evaluating the efficacy and safety of sonidegib. METHODS: Adults with no prior hedgehog pathway inhibitor therapy were randomized in a 1 : 2 ratio to sonidegib 200 mg or 800 mg once daily. Treatment continued for up to 42 months or until disease progression, unacceptable toxicity, death, study termination or withdrawal of consent. The primary efficacy end point was the objective response rate (ORR) by central review, assessed at baseline; weeks 5, 9 and 17; then subsequently every 8 or 12 weeks during years 1 or 2, respectively. Safety end points included adverse event monitoring and reporting. RESULTS: The study enrolled 230 patients, 79 and 151 in the 200‐mg and 800‐mg groups, respectively, of whom 8% and 3.3% remained on treatment by the 42‐month cutoff, respectively. The ORRs by central review were 56% [95% confidence interval (CI) 43–68] for laBCC and 8% (95% CI 0·2–36) for mBCC in the 200‐mg group and 46·1% (95% CI 37·2–55·1) for laBCC and 17% (95% CI 5–39) for mBCC in the 800‐mg group. No new safety concerns emerged. CONCLUSIONS: Sonidegib demonstrated sustained efficacy and a manageable safety profile. The final BOLT results support sonidegib as a viable treatment option for laBCC and mBCC. What's already known about this topic? Basal cell carcinoma (BCC) is usually treatable with surgery or radiation therapy, but there are limited treatment options for patients with advanced BCC. Sonidegib, a hedgehog pathway inhibitor approved for the treatment of advanced BCC, demonstrated clinically relevant efficacy and manageable safety in prior analyses of the phase II randomized, double‐blind BOLT study [Basal Cell Carcinoma Outcomes with LDE225 (sonidegib) Treatment]. What does this study add? This final 42‐month analysis of BOLT is the longest follow‐up available for a hedgehog pathway inhibitor. Clinically relevant efficacy results were sustained from prior analyses, with objective response rates by central review of the approved 200‐mg daily dose of 56% in locally advanced BCC and 8% in metastatic BCC. No new safety concerns were raised. The results confirmed sonidegib as a viable long‐term treatment option for patients with advanced BCC. John Wiley and Sons Inc. 2019-12-08 2020-06 /pmc/articles/PMC7318253/ /pubmed/31545507 http://dx.doi.org/10.1111/bjd.18552 Text en © 2019 The Authors. British Journal of Dermatology published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Dummer, R.
Guminksi, A.
Gutzmer, R.
Lear, J.T.
Lewis, K.D.
Chang, A.L.S.
Combemale, P.
Dirix, L.
Kaatz, M.
Kudchadkar, R.
Loquai, C.
Plummer, R.
Schulze, H.‐J.
Stratigos, A.J.
Trefzer, U.
Squittieri, N.
Migden, M.R.
Long‐term efficacy and safety of sonidegib in patients with advanced basal cell carcinoma: 42‐month analysis of the phase II randomized, double‐blind BOLT study
title Long‐term efficacy and safety of sonidegib in patients with advanced basal cell carcinoma: 42‐month analysis of the phase II randomized, double‐blind BOLT study
title_full Long‐term efficacy and safety of sonidegib in patients with advanced basal cell carcinoma: 42‐month analysis of the phase II randomized, double‐blind BOLT study
title_fullStr Long‐term efficacy and safety of sonidegib in patients with advanced basal cell carcinoma: 42‐month analysis of the phase II randomized, double‐blind BOLT study
title_full_unstemmed Long‐term efficacy and safety of sonidegib in patients with advanced basal cell carcinoma: 42‐month analysis of the phase II randomized, double‐blind BOLT study
title_short Long‐term efficacy and safety of sonidegib in patients with advanced basal cell carcinoma: 42‐month analysis of the phase II randomized, double‐blind BOLT study
title_sort long‐term efficacy and safety of sonidegib in patients with advanced basal cell carcinoma: 42‐month analysis of the phase ii randomized, double‐blind bolt study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318253/
https://www.ncbi.nlm.nih.gov/pubmed/31545507
http://dx.doi.org/10.1111/bjd.18552
work_keys_str_mv AT dummerr longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT guminksia longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT gutzmerr longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT learjt longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT lewiskd longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT changals longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT combemalep longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT dirixl longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT kaatzm longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT kudchadkarr longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT loquaic longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT plummerr longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT schulzehj longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT stratigosaj longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT trefzeru longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT squittierin longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy
AT migdenmr longtermefficacyandsafetyofsonidegibinpatientswithadvancedbasalcellcarcinoma42monthanalysisofthephaseiirandomizeddoubleblindboltstudy