Skin Basal Cell Carcinoma Clinical Trial
Official title:
A Phase 1b Open Label Study of Pembrolizumab for Unresectable or Metastatic Basal Cell Carcinoma
This phase 1-2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.
This study is a non-randomized evaluation of pembrolizumab as a treatment for unresectable or
metastatic basal cell carcinoma (BCC). Participants are assigned to treatment with
pembrolizumab plus vismodegib or pembrolizumab monotherapy on the basis of suitability for
treatment with smoothened (SMO) inhibitors such as vismodegib. Prospective participants who
have progressed on vismodegib, are intolerant to or have a medical contra-indication to
vismodegib may receive pembrolizumab monotherapy. Because treatment is non-randomized, no
comparison between treatment groups is conducted.
PRIMARY OBJECTIVE To assess the overall response rate (ORR) of unresectable or metastatic BCC
patients to pembrolizumab with or without vismodegib (all evaluable patients) at 18 weeks
SECONDARY OBJECTIVES
- To assess the ORR of unresectable or metastatic BCC patients to pembrolizumab
monotherapy at 18 weeks
- To assess the ORR of unresectable or metastatic BCC patients to pembrolizumab
monotherapy at 9 weeks
- To assess ORR of unresectable or metastatic BCC patients to pembrolizumab plus
vismodegib at 18 weeks
- To assess ORR of unresectable or metastatic BCC patients to pembrolizumab plus
vismodegib at 9 weeks
- To assess the safety and tolerability of pembrolizumab (either monotherapy or
combination therapy) for unresectable or metastatic BCC.
- To assess the duration of response after pembrolizumab (either monotherapy or
combination therapy)
- Incidence and severity of adverse events
- Correlative studies including programmed death-ligand 1 (PD-L1) expression
pre-treatment, lymphocytic infiltrates pre- and post-treatment, mutational analysis pre-
and post-treatment
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