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Original Investigation |

Hedgehog Pathway Inhibitor Therapy for Locally Advanced and Metastatic Basal Cell Carcinoma A Systematic Review and Pooled Analysis of Interventional Studies

Audrey A. Jacobsen, BA1; Adam S. Aldahan, BS1; Olivia B. Hughes, BS1; Vidhi V. Shah, BA1; John Strasswimmer, MD, PhD1
[+] Author Affiliations
1University of Miami Miller School of Medicine, Miami, Florida
JAMA Dermatol. 2016;152(7):816-824. doi:10.1001/jamadermatol.2016.0780.
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Importance  Hedgehog pathway inhibitors (HPIs) were made available by US Food and Drug Administration approval in 2012 for vismodegib and 2015 for sonidegib. Both target the Smoothened molecule and are indicated for locally advanced basal cell carcinoma (laBCC) and metastatic basal cell carcinoma (mBCC).

Objective  To evaluate clinical experience with HPIs, including efficacy and adverse effects.

Data Sources  We conducted a systematic review in concordance with the PRISMA guidelines of PubMed, the Cochrane Central Register of Controlled Trials, ClinicalTrials.gov, and EMBASE, using search terms “vismodegib,” “sonidegib,” “Erivedge,” “Odomza,” “basal cell carcinoma,” and “BCC.”

Study Selection  We included clinical trials, retrospective medical record reviews, and prospective case series that used HPIs for the treatment of laBCC or mBCC in human subjects. Individual case reports and limited, retrospective case series were excluded from our review.

Data Extraction and Synthesis  Data were extracted independently by 2 reviewers on a predesigned, standardized form.

Main Outcomes and Measures  The following data were recorded: number of patients with laBCC or mBCC, dose and frequency of drug administration, median duration of treatment, clearance and recurrence rates, and adverse effects.

Results  Eleven vismodegib articles (published between 2009 and 2015) met criteria for inclusion, and 8 articles were able to be pooled for analysis. The 8 pooled articles included 744 total patients with 704 patients clinically evaluable. Sonidegib did not yield enough publications for a formal analysis. Objective response to vismodegib for laBCC had a weighted average of 64.7% (95% CI, 63.7%-65.6%); complete response averaged 31.1% (95% CI, 30.4%-31.8%). Objective response for mBCC was 33.6% (95% CI, 33.1%-34.2%); complete response averaged 3.9% (95% CI, 3.3%-4.4%). Median duration of therapy was 35.8 weeks (95% CI, 35.1-36.5 weeks).

Conclusions and Relevance  In a systematic review of HPIs for laBCC and mBCC, vismodegib, but not sonidegib, had enough studies to warrant a pooled analysis. Vismodegib was identified to have a significant, consistent effect on the median duration of therapy of laBCC and mBCC. While mBCC responses are superior to any traditional approach, the response rate for laBCC might be considered in the context of other standard treatment options including surgery and radiation therapy.

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Figure.
Flow Diagram of Article Selection Process According to PRISMA Guidelines

Overall, 10 studies using vismodegib met search criteria for inclusion in our systematic review and pooled analysis; 1 additional article that is in press was added for completeness. Eight of 11 vismodegib articles were able to be pooled for analysis. Sonidegib did not yield enough results to merit a pooled analysis.

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