Skip to main content
NCBI home page
Drugs in Context logoLink to Drugs in Context
. 2022 May 23;11:2022-3-8. doi: 10.7573/dic.2022-3-8

Experience with sonidegib in patients with advanced basal cell carcinoma: case reports

Susana Puig 1,2,✉, Carlos Serra-Guillén 3, Gemma Pérez-Pastor 4, Álvaro Martínez-Domenech 4, Ricardo Fernández-de-Misa Cabrera 5
PMCID: PMC9132536  PMID: 35677182

Abstract

Sonidegib is a Hedgehog signalling pathway inhibitor approved for use in patients with advanced basal cell carcinoma (BCC) not eligible for surgery or radiotherapy. This report describes clinical experience with sonidegib in two patients with locally advanced BCC (one with a tumour adjacent to the right eye and the other with a tumour associated with the left ear) and in one patient with Gorlin syndrome. Two of the patients had recurrent and intractable tumours. Treatment with sonidegib 200 mg/day led to remission in both patients with locally advanced BCC within 7 months and to a reduction in the size and number of lesions after 4 months in the patient with Gorlin syndrome. Adverse effects reported in these patients were cramps, alopecia, ageusia and weight loss, all of which were mild and consistent with the known toxicity profile for sonidegib. Sonidegib has an important role to play in the effective treatment of challenging cases of advanced BCC. In parallel, a need remains to improve management protocols for patients with advanced BCC, particularly through earlier intervention and a multidisciplinary team approach.

Keywords: case reports, Gorlin syndrome, locally advanced basal cell carcinoma, sonidegib, vismodegib

Introduction

Non-melanoma skin cancer is the fifth most commonly occurring cancer in men and women globally.1 Basal cell carcinoma (BCC) accounts for the majority (~80%) of non-melanoma skin cancer cases,2,3 and the incidence has been increasing worldwide since the 1970s.3,4 People with white skin are most susceptible to BCC, with sun-exposed areas, such as the head and neck, being particularly vulnerable.2,5

As BCC tumours are generally slow growing, the condition is highly treatable if detected early and managed appropriately.3 Metastatic BCC (mBCC) is extremely rare (0.003–0.55% of cases)2 but, when it does occur, the prognosis is poor.3 Large, aggressive or recurrent BCC tumours, and those which penetrate deeper into the skin or associated tissues, are referred to as locally advanced BCC (laBCC). laBCC poses several therapeutic challenges: the tumours may not be amenable to radiation therapy, surgery may be impractical due to the risk of morbidity, loss of function or disfigurement, and risk of recurrence is high.3 Until relatively recently, mBCC and laBCC were considered untreatable conditions, with palliative care being the only option.

The Hedgehog (Hh) signalling pathway is involved primarily in embryonic development and control of gene activation. Normally suppressed in adults, aberrant activation of the Hh pathway through gene mutations or excessive expression of Hh signalling molecules can lead to development of certain cancers, including BCC and Gorlin syndrome. ‘Smoothened’ (SMO), a transmembrane protein and main transducer of the Hh signalling pathway, initiates a signalling cascade that increases the expression of glioma-associated oncogene transcription factors. By binding to SMO, Hh pathway inhibitors (HPIs) prevent downstream activation of Hh pathway signalling.6,7

Vismodegib was approved in 2012 for treatment of adults with mBCC or laBCC not eligible for surgery or radiotherapy.8 Subsequent approval of sonidegib in 2015 provided an alternative option for laBCC patients.9,10 European consensus guidelines recommend that patients with mBCC or laBCC be offered treatment with vismodegib or sonidegib.11 Although the compounds share the same mechanism of action,12,13 their pharmacokinetic profiles differ. Notably, sonidegib has a large volume of distribution, as indicated by steady-state concentrations sixfold higher in skin than in plasma, whereas vismodegib is confined mainly to the plasma and extracellular spaces.10,14,15

The efficacy of sonidegib was established in the phase II, multicentre, randomized, double-blind BOLT (Basal Cell Carcinoma Outcomes with LDE225 [sonidegib] Treatment) study in adults with histologically confirmed laBCC or mBCC not amenable to curative surgery or radiotherapy.16–19 Cut-off for the final analysis was 42 months.19 The primary endpoint was the objective response rate (ORR) by central review (ORR-CR), defined as the proportion of patients with complete or partial response assessed by the BCC-modified Response Evaluation Criteria in Solid Tumors (mRECIST). ORR by investigator review (ORR-IR) was a secondary endpoint. In the final analysis, the ORR-CR was 56.1% and the ORR-IR was 71.2% as per mRECIST in patients with laBCC.20,21 A pre-planned sensitivity analysis compared these efficacy outcomes with those obtained using the composite RECIST criteria (≥30% reduction in externally visible tumour or radiographic dimension, or complete ulceration resolution) applied in the ERIVANCE study of vismodegib.21,22 Based on these less stringent RECIST criteria, efficacy outcomes with sonidegib were even higher, with an ORR-CR and ORR-IR of 60.6% and 74.2%, respectively.20 Irrespective of the criteria used to assess response, long-term positive responses to sonidegib 200 mg/day were similar for patients with aggressive or non-aggressive histological subtypes of laBCC.20,23

The safety profile of sonidegib was consistent throughout the course of the BOLT study. Median duration of exposure to sonidegib 200 mg/day was 11 months, with 24% of patients having ≥20 months’ exposure. Adverse effects (AEs) were mainly grade 1/2 in severity. The most common AEs (≥25% of patients) were muscle spasms, alopecia, dysgeusia, nausea, elevated creatine kinase, weight decrease, fatigue and decreased appetite. Grade 3/4 treatment-related AEs and serious treatment-related AEs were reported in 32% and 5% of patients, respectively. Common AEs requiring treatment interruption or a dosage reduction were elevated creatine kinase, nausea, vomiting, diarrhoea and elevated lipase. Most AEs were manageable and reversible with dose interruptions, with no overall impact on efficacy.19

Given that the strict adherence to protocol required in randomized controlled trials can limit generalizing the results to external populations, interventions must also be evaluated under real-world conditions.24 Herein, we present clinical experience with sonidegib in three patients with advanced BCC.

Patient consent

All data presented in this article have been de-identified to ensure patient confidentiality. Patient consent was not required.

Case reports

Case 1

A 79-year-old woman (height 1.46 m; weight 72 kg) presented to Dermatology Services at the Hospital Universitario Nuestra Señora de Candelaria, Tenerife, Spain, in September 2017 for a pruritic facial lesion of slow evolution over recent years. Examination revealed an erythematous plaque of approximately 13 × 8 mm adjacent to the caruncle of the right eye, with some telangiectasia on the surface. The diagnosis was laBCC. Comorbidities were cholecystectomy, euthyroid goitre and high blood pressure. The patient was sensitized to moxifloxacin.

A biopsy in January 2018 confirmed a diagnosis of BCC with an infiltrative pattern. The patient underwent maxillofacial surgery and was referred for radiation therapy (80 kV X-rays at a daily dose of 300 cGy, reaching a total dose of 4800 cGY) ending on 8 February 2018. She achieved a complete clinical remission.

In October 2019, the tumour recurred and the patient was referred for Mohs micrographic surgery. Due to the COVID pandemic, she declined transfer to mainland Spain, which delayed the consultant oncological dermatology assessment until March 2020. At assessment, an erythematous and crusty plaque of approximately 16 × 8 mm located in the immediate vicinity of the caruncle of the right eye was evident. No adenopathies, masses or megaly were palpated. No significant laboratory abnormalities were identified, and magnetic resonance imaging (MRI) was negative for intraorbital invasion (Figure 1). The patient had an Eastern Cooperative Oncology Group Performance Status of 0.

Figure 1.

Figure 1

Open in a new tab

Case 1: MRI scan of a female patient with a recurrent basal cell carcinoma adjacent to the caruncle of the right eye, showing no intra-orbital invasion.

Sonidegib 200 mg/day was prescribed, beginning 26 August 2020, based on published evidence of its efficacy in laBCC. Tumour evolution is shown in Figure 2. A response was evident within the first month of treatment. By 19 March 2021 (7 months after treatment commencement), the patient had achieved a complete clinical response. After confirming the clinical response by control biopsy, sonidegib was discontinued on 27 May 2021 (after 9 months). In February 2022, 9 months after treatment discontinuation, the patient remained in remission.

Figure 2.

Figure 2

Open in a new tab

Case 1: Clinical presentation of a basal cell carcinoma in a female patient: (a) pre-treatment, (b) at 1 month (clinical response) and (c) at 1 year (continued remission) after treatment with sonidegib 200 mg/day (for 9 months).

Throughout treatment, the patient experienced mild toxicity consisting of grade 1 cramping, ageusia and weight loss. Three months after discontinuing sonidegib, all AEs had resolved.

Case 2

A 69-year-old man was referred for a tumour located in the left ear. The tumour had developed over 6 years, growing slowly until it occupied about two-thirds of the ear, with occasional bleeding. A biopsy indicated metatypical BCC with a mixed pattern (nodular and infiltrative). The patient had no comorbidities and was not receiving any chronic medication.

Examination revealed a plaque of 4 × 3 cm in the helix and antihelix of the left ear, poorly delimited, with retraction of the pinna. The plaque was infiltrated, with clinical evidence of cartilage involvement. The clinical diagnosis was BCC ulcus rodens.

In November 2020, the patient began treatment with sonidegib 200 mg/day. Improvement was evident after 2 months and, by 6 months, a complete clinical response was achieved (Figure 3). A biopsy including cartilage indicated no evidence of tumour.

Figure 3.

Figure 3

Open in a new tab

Case 2: Clinical presentation of a metatypical basal cell carcinoma with a mixed nodular and infiltrative pattern in a male patient: (a) pre-treatment and (b) after 6 months of treatment with sonidegib 200 mg/day.

Sonidegib was well tolerated by this patient, with grade 1 alopecia being the only reported AE. Due to good tolerability, and in the presence of a complete clinical and histological response, sonidegib treatment was continued for 6 months after complete clinical response.

Case 3

A 38-year-old man with a long-term history of Gorlin syndrome (nevoid basal cell carcinoma syndrome) had been in dermatological follow-up since childhood. He had no comorbidities and was not receiving any chronic medication.

From the age of 8 years, the patient had been treated for multiple BCCs by surgery, cryotherapy and electrocoagulation. Most lesions were located on the face and scalp. Mohs surgery was required on some occasions to treat infiltrative pattern lesions. Oral surgery was performed as needed to remove several mandibular keratocysts.

Due to an acceleration of BCCs at the time of consultation, the patient was treated with vismodegib 150 mg/day from November 2019 to October 2020. Treatment response was good, with complete disappearance of lesions. AEs were mild: grade 2 alopecia and grade 1 cramps.

Three months after stopping vismodegib, the lesions began to recur. In May 2021, the patient presented with more than 50 lesions on his face and scalp, mostly pigmented BCCs 4–6 mm in diameter and some ulcerated. Due to the patient’s concerns about AEs experienced during treatment with vismodegib, sonidegib 200 mg/day was selected.

In September 2021, after 4 months of sonidegib treatment, there was a decrease in the number and size of the lesions (Figure 4). The only side effect the patient experienced was grade 1 alopecia and self-reported changes in hair texture. Laboratory tests performed during follow-up (at 1 month and every 2 months thereafter) showed no abnormalities.

Figure 4.

Figure 4

Open in a new tab

Case 3: Gorlin syndrome lesions on the forehead of the patient: (a) pre-treatment and (b) after 4 months of treatment with sonidegib 200 mg/day.

After 6 months of treatment with sonidegib, a complete clinical response in all lesions was observed. With the patient’s agreement, treatment was discontinued with a plan to reassess clinically every 3–6 months and reintroduce sonidegib intermittently between rest periods as necessary.

The patient tolerated sonidegib better than vismodegib. He was satisfied with sonidegib treatment with no need to implement every-other-day dosing.

Clinical overview

Periocular localization of BCC (Case 1) with lesion development adjacent to and invasion through the caruncle is appropriately diagnosed as laBCC. The patient’s response to sonidegib was notably rapid (within 1 month), consistent with that described in a man with laBCC of the nuchal region who had a 95% reduction in tumour size 3 months after starting treatment with sonidegib 200 mg/day;25 a 71-year-old man with clinically important tumour regression within 2 months of starting sonidegib 200 mg/day for multiple laBCC, including on the internal canthus;26 and a 63-year-old man who had a marked response after 2 weeks of treatment with sonidegib 200 mg/day for multiple laBCC lesions of the face, including a 4-year evolving ulcerated lesion under the right lower eyelid.27

The patient with metatypical BCC (mixed nodular and infiltrative pattern) of the left ear (Case 2) also showed an excellent response to sonidegib, achieving a complete clinical response after 6 months of treatment. Numerous other case reports or case series have documented clinical improvement or clearance of laBCC lesions, including complete responses, with sonidegib 200 mg/day most often within a few months of treatment start.28–34 There are also anecdotal reports of the effectiveness of sonidegib for locally advanced basosquamous carcinomas,31 locally advanced anal and rectal BCC,35 and in combination with fractionated radiation for recurrent advanced BCC of the head and neck.36

Case 3 shows the promising effectiveness of sonidegib for the treatment of Gorlin syndrome, including in patients with disease recurrence after receiving vismodegib, which is supported by the collective clinical experience of a multidisciplinary expert panel pointing to optimal responses to HPIs in these patients.37 Italian investigators reported the case of an 89-year-old woman with Gorlin syndrome who had been treated successfully with vismodegib but had to discontinue treatment due to severe asthenia; all lesions relapsed after discontinuation. After 3 months of treatment with sonidegib 200 mg/day, partial re-epithelization and tumour shrinkage were observed in all target lesions, with no AEs. At 6 months, there was further improvement and complete healing of lesions on the face, again without AEs.38 This outcome, together with Case 3 herein, shows that lesion recurrence after HPI discontinuation following response does not constitute resistance. As such, rechallenge with a drug of the same class should be considered before switching to a completely different treatment such as second-line immunotherapy.

The usefulness of switching between HPIs was also reported in a case involving an 87-year-old man with inoperable laBCC involving the sinuses, nasal cavity and brain. Sonidegib 200 mg/day in combination with itraconazole pulse dosed at 100 mg/day (2 weeks on, 2 weeks off) was effective whereas previous vismodegib had proved inadequate. Vismodegib successfully reduced tumour size by 70% over 3 months when tumour involvement was limited to the nasal cavity and sinuses, but the effects diminished over time. Vismodegib was discontinued and the patient received radiation therapy (total dose of 70 Gy). Two years later, BCC recurred and, despite vismodegib treatment for 6 months, the lesions progressed. Pembrolizumab was tried without success, and the tumour progressed into the brain. Sonidegib/itraconazole combination therapy led to significant improvement after 3 months. After approximately 8 months, the intracranial lesion was no longer visible on MRI and the intranasal and sinus lesions were stable and improved.39 Treatment resistance in patients receiving HPIs may be due to the development of SMO mutations, which impair effective binding. The efficacy of an alternative HPI in this setting may depend on the specific mutation, the binding location of the drug and whether the mutation produces a conformational change influencing drug binding. Identifying biomarkers of resistance or response would be useful to target HPIs to patients most likely to benefit.40

Follow-up of patients with laBCC is of considerable interest to establish whether full lesion clearance can be achieved and whether tolerability is maintained during continued treatment. Our experience suggests that clinical follow-up every 3–6 months during maintenance treatment is appropriate. After discontinuation, consideration can be given to reintroducing sonidegib upon the appearance of multiple new lesions. An alternative approach is to continue sonidegib at reduced dosing (every other day or twice a week) as maintenance therapy. For patients with chronic Gorlin syndrome, a suitable treatment protocol may be sonidegib 200 mg/day until lesion clearance, alternating with no treatment during periods of remission. Irrespective of the condition being treated, any decisions regarding long-term management should be discussed and agreed with the patient. Telemedicine can be a useful adjunct tool for patients who are able to provide digital photos of their lesions of suitable standard for comparison with previous images.29

Two of our patients (Cases 2 and 3) reported alopecia as the sole AE to sonidegib, and both opted to continue treatment. The remaining patient (Case 1) experienced mild cramps, ageusia and weight loss, all of which resolved once treatment was discontinued. These AEs are within the established toxicity profile of sonidegib.9 In the BOLT study, AEs were common but rarely serious in patients receiving sonidegib. At final analysis at 42 months, alopecia (grade ≤2) had been reported in 49% of patients receiving sonidegib 200 mg/day.19 HPIs may induce alopecia by interfering with the transition of follicles from the telogen phase of hair shedding to the anagen growth phase.41 The most common grade 3–4 AEs associated with sonidegib 200 mg/day in the BOLT study were elevated creatine and lipase (each in 6% of patients).19 Elevated creatine levels are also associated with vismodegib,42 suggesting that this is a class effect. No abnormal laboratory data were recorded in any of the three cases presented.

Most AEs associated with HPI treatment are thought to result from inhibition of the Hh signalling pathway in normal tissue. Although generally not severe, AEs can be persistent, reducing patients’ quality of life and necessitating treatment interruption or discontinuation. Indeed, it has been suggested that some patients with laBCC who discontinue HPI therapy due to AEs do so because their intolerance for AEs begins to outweigh the extent of clinical improvement. Healthcare professionals need to be aware of this possibility and manage patients accordingly in order to facilitate continued treatment, if appropriate.19,41 With respect to sonidegib, a retrospective case series of 20 patients43 and a post hoc analysis of the BOLT study44 found that dose adjustments (e.g. dose reductions, alternate day dosing) or treatment delays were practical solutions to reduce the need for treatment discontinuation with no detriment to sonidegib efficacy. Prior to initiating HPI therapy in patients with laBCC receiving statin therapy, it may be prudent to stabilize the patient on a low dose of a hydrophilic statin (e.g. rosuvastatin) not metabolized by CYP 3A4 to reduce the risk of muscle-related AEs.45 The use of concurrent superficial radiotherapy at the time of maximal therapeutic effect of an HPI led to a high clinical response rate with minimal toxicity in a retrospective review of 12 patients with laBCC treated with vismodegib or sonidegib, and merits further investigation in well-controlled clinical trials.46

Conclusions

Collectively, case reports/case series of sonidegib use in clinical practice support its effectiveness in patients with advanced BCC, as demonstrated in the BOLT study.16–20 Although based on only three cases, and with treatment ongoing in two of these cases at the time of case submission, the clinical experience with sonidegib presented herein demonstrates its ability to induce tumour remission in patients with laBCC or Gorlin syndrome, including recurrent and intractable cases. AEs recorded with sonidegib in these patients were mild and manageable, consistent with its known safety profile. Importantly, strategies such as dose reductions and treatment interruptions to manage patients unable to tolerate dosing schedules or with suspected treatment-related AEs do not appear to undermine sonidegib efficacy and may improve patient outcomes by preventing treatment discontinuations. Overall, sonidegib appears to be a useful addition to the therapeutic armamentarium for patients with advanced BCC, showing efficacy in patients who have previously failed on vismodegib.

Despite the wealth of high-quality evidence regarding therapeutic options for laBCC, delays in disease management are not uncommon in these patients, even in centres with active multidisciplinary teams. As such, continued efforts are required to define and implement optimal care for patients with advanced BCC.

Acknowledgements

Preparation of this manuscript was assisted by medical writers on behalf of Content Ed Net.

Footnotes

Contributions: Conception and design: all authors; clinical data: CS-G, GP-P, AM-D and RFdMC; critical review of the manuscript: all authors. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole and have given their approval for this version to be published.

Disclosure and potential conflicts of interest: SP has received honoraria as speaker or for participating in advisory boards from Regeneron, Roche, Sanofi and Sun Pharma. CS-G has received honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from Sun Pharma; and payment for expert testimony from Sun Pharma. GP-P has received honoraria as speaker or for participating in advisory boards from Amgen and Sun Pharma. AM-D has no conflicts of interest to declare. RFdMC has received consulting fees and/or honoraria for expert testimony from Sun Pharma; honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from Kyowa, MSD and Takeda; support for attending meetings and/or travel from Kyowa, Sun Pharma and Takeda; participation on a Data Safety Monitoring Board or Advisory Board for Sun Pharma; member of non-melanoma skin cancer expert committee. The International Committee of Medical Journal Editors (ICMJE) Potential Conflicts of Interests form for the authors is available for download at: https://www.drugsincontext.com/wp-content/uploads/2022/05/dic.2022-3-8-COI.pdf

Funding declaration: Editorial and writing assistance was funded by SUN Pharmaceuticals, Hoofddorp, The Netherlands.

Correct attribution: Copyright © 2022 Puig S, Serra-Guillén C, Pérez-Pastor G, Martínez-Domenech A, Fernández-de-Misa Cabrera R. https://doi.org/10.7573/dic.2022-3-8. Published by Drugs in Context under Creative Commons License Deed CC BY NC ND 4.0.

Drugs in Context is published by BioExcel Publishing Ltd. Registered office: Plaza Building, Lee High Road, London, England, SE13 5PT.

BioExcel Publishing Limited is registered in England Number 10038393. VAT GB 252 7720 07.

For all manuscript and submissions enquiries, contact the Editorial office editorial@drugsincontext.com

For all permissions, rights and reprints, contact David Hughes david.hughes@bioexcelpublishing.com

Provenance: Submitted; externally peer reviewed.

References

  • 1.World Cancer Research Fund International. Skin cancer statistics. [Accessed 29 October 2021.]. https://www.wcrf.org/dietandcancer/skin-cancer-statistics/
  • 2.Rubin AI, Chen EH, Ratner D. Basal-cell carcinoma. N Engl J Med. 2005;353(21):2262–2269. doi: 10.1056/NEJMra044151. [DOI] [PubMed] [Google Scholar]
  • 3.Migden MR, Chang ALS, Dirix L, et al. Emerging trends in the treatment of advanced basal cell carcinoma. Cancer Treat Rev. 2018;64:1–10. doi: 10.1016/j.ctrv.2017.12.009. [DOI] [PubMed] [Google Scholar]
  • 4.American Academy of Dermatology Association. Skin cancer. [Accessed 28 October 2021.]. https://www.aad.org/media/stats-skin-cancer .
  • 5.Rogers HW, Weinstock MA, Feldman SR, et al. Incidence estimate of nonmelanoma skin cancer (keratinocyte carcinomas) in the U.S. population, 2012. JAMA Dermatol. 2015;151(10):1081–1086. doi: 10.1001/jamadermatol.2015.1187. [DOI] [PubMed] [Google Scholar]
  • 6.Sekulic A, Mangold AR, Northfelt DW, et al. Advanced basal cell carcinoma of the skin: targeting the hedgehog pathway. Curr Opin Oncol. 2013;25(3):218–223. doi: 10.1097/CCO.0b013e32835ff438. [DOI] [PubMed] [Google Scholar]
  • 7.Skoda AM, Simovic D, Karin V, et al. The role of the hedgehog signaling pathway in cancer: A comprehensive review. Bosn J Basic Med Sci. 2018;18(1):8–20. doi: 10.17305/bjbms.2018.2756. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.European Medicines Agency. Erivedge. Summary of Product Characteristics. [Accessed 4 February 2022.]. https://www.ema.europa.eu/en/documents/product-information/erivedge-epar-product-information_en.pdf .
  • 9.European Medicines Agency. Odomzo. Summary of Product Characteristics. [Accessed 4 February 2022.]. https://www.ema.europa.eu/en/documents/product-information/odomzo-epar-product-information_en.pdf .
  • 10.Dummer R, Ascierto PA, Basset-Seguin N, et al. Sonidegib and vismodegib in the treatment of patients with locally advanced basal cell carcinoma: a joint expert opinion. J Eur Acad Dermatol Venereol. 2020;34(9):1944–1956. doi: 10.1111/jdv.16230. [DOI] [PubMed] [Google Scholar]
  • 11.Peris K, Fargnoli MC, Garbe C, et al. Diagnosis and treatment of basal cell carcinoma: European consensus-based interdisciplinary guidelines. Eur J Cancer. 2019;118:10–34. doi: 10.1016/j.ejca.2019.06.003. [DOI] [PubMed] [Google Scholar]
  • 12.Gould SE, Low JA, Marsters JC, Jr, et al. Discovery and preclinical development of vismodegib. Expert Opin Drug Discov. 2014;9(8):969–984. doi: 10.1517/17460441.2014.920816. [DOI] [PubMed] [Google Scholar]
  • 13.Jain S, Song R, Xie J. Sonidegib: mechanism of action, pharmacology, and clinical utility for advanced basal cell carcinomas. OncoTargets Ther. 2017;10:1645–1653. doi: 10.2147/OTT.S130910. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Brancaccio G, Pea F, Moscarella E, Argenziano G. Sonidegib for the treatment of advanced basal cell carcinoma. Front Oncol. 2020;10:582866. doi: 10.3389/fonc.2020.582866. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Migden M, Farberg AS, Dummer R, et al. A review of hedgehog inhibitors sonidegib and vismodegib for treatment of advanced basal cell carcinoma. J Drugs Dermatol. 2021;20(2):156–165. doi: 10.36849/JDD.5657. [DOI] [PubMed] [Google Scholar]
  • 16.Migden MR, Guminski A, Gutzmer R, et al. 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. Lancet Oncol. 2015;16(6):716–728. doi: 10.1016/S1470-2045(15)70100-2. [DOI] [PubMed] [Google Scholar]
  • 17.Dummer R, Guminski A, Gutzmer R, et al. The 12-month analysis from basal cell carcinoma outcomes with LDE225 treatment (BOLT): A phase II, randomized, double-blind study of sonidegib in patients with advanced basal cell carcinoma. J Am Acad Dermatol. 2016;75(1):113–125e5. doi: 10.1016/j.jaad.2016.02.1226. [DOI] [PubMed] [Google Scholar]
  • 18.Lear JT, Migden MR, Lewis KD, et al. Long-term efficacy and safety of sonidegib in patients with locally advanced and metastatic basal cell carcinoma: 30-month analysis of the randomized phase 2 BOLT study. J Eur Acad Dermatol Venereol. 2018;32(3):372–381. doi: 10.1111/jdv.14542. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Dummer R, Guminksi A, Gutzmer R, et al. 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. Br J Dermatol. 2020;182(6):1369–1378. doi: 10.1111/bjd.18552. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Gutzmer R, Robert C, Loquai C, et al. Assessment of various efficacy outcomes using ERIVANCE-like criteria in patients with locally advanced basal cell carcinoma receiving sonidegib: results from a preplanned sensitivity analysis. BMC Cancer. 2021;21(1):1244. doi: 10.1186/s12885-021-08968-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Sekulic A, Migden MR, Oro AE, et al. Efficacy and safety of vismodegib in advanced basal-cell carcinoma. N Engl J Med. 2012;366:2171–2179. doi: 10.1056/NEJMoa1113713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Sekulic A, Migden MR, Basset-Seguin N, et al. Long-term safety and efficacy of vismodegib in patients with advanced basal cell carcinoma: final update of the pivotal ERIVANCE BCC study [published correction appears in BMC Cancer. 2019; 19:366] BMC Cancer. 2017;17:332. doi: 10.1186/s12885-017-3286-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Dummer R, Lear JT, Guminski A, et al. Efficacy of sonidegib in histologic subtypes of advanced basal cell carcinoma: Results from the final analysis of the randomized phase 2 basal cell carcinoma outcomes with LDE225 treatment (BOLT) trial at 42 months. J Am Acad Dermatol. 2021;84(4):1162–1164. doi: 10.1016/j.jaad.2020.08.042. [DOI] [PubMed] [Google Scholar]
  • 24.Concato J. Study design and “evidence” in patient-oriented research. Am J Respir Crit Care Med. 2013;187(11):1167–1172. doi: 10.1164/rccm.201303-0521OE. [DOI] [PubMed] [Google Scholar]
  • 25.Villani A, Fabbrocini G, Costa C, et al. Complete remission of an advanced basal cell carcinoma after only 3-month treatment with sonidegib: Report of a case and drug management during COVID-19 pandemic. Dermatol Ther. 2020;33(6):e14200. doi: 10.1111/dth.14200. [DOI] [PubMed] [Google Scholar]
  • 26.Tarantino V, Zavattaro E, Veronese F, et al. Rapid and exceptional response to sonidegib in a patient with multiple locally advanced basal cell carcinomas. Anticancer Drugs. 2021;32(4):465–468. doi: 10.1097/CAD.0000000000001054. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Trabelsi S, Khidher F. Rapid onset of response to sonidegib for multiple facial basal cell carcinomas during COVID-19 pandemic. Dermatol Ther. 2022;35(4):e15317. doi: 10.1111/dth.15317. [DOI] [PubMed] [Google Scholar]
  • 28.Gibson M, Murrell DF. Drug-related adverse effects of vismodegib and sonidegib for locally advanced or metastatic basal cell carcinoma. Australas J Dermatol. 2020;61(2):176–177. doi: 10.1111/ajd.13205. [DOI] [PubMed] [Google Scholar]
  • 29.Conforti C, Giuffrida R, Di Meo N, Zalaudek I. Management of locally advanced basal cell carcinoma treated with sonidegib: The experience of an Italian reference hospital. Dermatol Ther. 2020;33(6):e14511. doi: 10.1111/dth.14511. [DOI] [PubMed] [Google Scholar]
  • 30.Moscarella E, Brancaccio G, Briatico G, et al. Management of advanced basal cell carcinoma: Real-life data with sonidegib. Dermatol Ther. 2021;34(3):e14948. doi: 10.1111/dth.14948. [DOI] [PubMed] [Google Scholar]
  • 31.Toffoli L, Conforti C, Zelin E, et al. Locally advanced basal cell carcinoma: Real-life data with sonidegib. Dermatol Ther. 2022. p. e15441. [DOI] [PubMed]
  • 32.Leow LJ, Teh N. Clinical clearance of complex basal cell carcinoma in patients receiving sonidegib: A case series. Dermatol Ther. 2022;35(2):e15217. doi: 10.1111/dth.15217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Villani A, Fabbrocini G, Scalvenzi M. Sonidegib treatment in patients with locally advanced basal cell carcinoma. Dermatol Ther. 2022;35(4):e15348. doi: 10.1111/dth.15348. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Villani A, Fabbrocini G, Costa C, Scalvenzi M. Sonidegib efficacy and tolerability in advanced basal cell carcinoma: A single-center real-life experience. J Am Acad Dermatol. 2022;86(4):e175. doi: 10.1016/j.jaad.2021.11.041. [DOI] [PubMed] [Google Scholar]
  • 35.Conforti C, Toffoli L, Degrassi F, di Meo N, Zalaudek I. Anal and rectal locally advanced basal cell carcinoma treated with sonidegib. Dermatol Ther. 2022;35(2):e15242. doi: 10.1111/dth.15242. [DOI] [PubMed] [Google Scholar]
  • 36.Wang K, Patel M, Prabhu AV, Lewis GD. First reported case of concurrent sonidegib and radiotherapy for recurrent, advanced basal cell carcinoma. Rep Pract Oncol Radiother. 2021;26(1):149–152. doi: 10.5603/RPOR.a2021.0010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Yoon J, Apicelli AJ, III, Pavlopoulos TV. Intracranial regression of an advanced basal cell carcinoma using sonidegib and itraconazole after failure with vismodegib. JAAD Case Reports. 2017;4(1):10–12. doi: 10.1016/j.jdcr.2017.11.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Piccerillo A, Di Stefani A, Costantini A, et al. Sonidegib after vismodegib discontinuation in a patient with Gorlin-Goltz syndrome and multiple basal cell carcinomas. Dermatol Ther. 2021;34(5):e15095. doi: 10.1111/dth.15095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Doan HQ, Chen L, Nawas Z, et al. Switching hedgehog inhibitors and other strategies to address resistance when treating advanced basal cell carcinoma. Oncotarget. 2021;12(20):2089–2100. doi: 10.18632/oncotarget.28080. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.De Giorgi V, Scarfì F, Trane L, et al. Treatment of advanced basal cell carcinoma with hedgehog pathway inhibitors: a multidisciplinary expert meeting. Cancers. 2021;13(22):5706. doi: 10.3390/cancers13225706. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Lacouture ME, Dréno B, Ascierto PA, et al. Characterization and management of hedgehog pathway inhibitor-related adverse events in patients with advanced basal cell carcinoma. Oncologist. 2016;21(10):1218–1229. doi: 10.1634/theoncologist.2016-0186. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Basset-Séguin N, Hauschild A, Kunstfeld R. Vismodegib in patients with advanced basal cell carcinoma: Primary analysis of STEVIE, an international, open-label trial. Eur J Cancer. 2017;86:334–348. doi: 10.1016/j.ejca.2017.08.022. [DOI] [PubMed] [Google Scholar]
  • 43.Villani A, Costa C, Fabbrocini G, et al. Dose reduction during routine treatment of locally advanced basal cell carcinoma with the hedgehog inhibitor sonidegib to manage adverse effects: A retrospective case series. J Am Acad Dermatol. 2021;84(4):e211–e212. doi: 10.1016/j.jaad.2020.12.006. [DOI] [PubMed] [Google Scholar]
  • 44.Lewis K, Dummer R, Farberg AS, et al. Effects of sonidegib following dose reduction and treatment interruption in patients with advanced basal cell carcinoma during 42-month BOLT trial. Dermatol Ther. 2021;11(6):2225–2234. doi: 10.1007/s13555-021-00619-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Trane L, Silvestri F, Venturi F, et al. The clinical impact of hedgehog pathway inhibitors and statin therapy in the treatment of locally advanced basal cell carcinoma: a case report. Dermatol Ther. 2022;35(1):e15191. doi: 10.1111/dth.15191. [DOI] [PubMed] [Google Scholar]
  • 46.Weissman JP, Samlowski W, Meoz R. Hedgehog inhibitor induction with addition of concurrent superficial radiotherapy in patients with locally advanced basal cell carcinoma: a case series. Oncologist. 2021;26(12):e2247–e2253. doi: 10.1002/onco.13959. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Drugs in Context are provided here courtesy of BioExcel Publishing Ltd

RESOURCES