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Hedgehog Inhibitors Beyond Clinical Complete Response in Basal Cell Carcinoma: Should I Stop or Should I Go?

Authors :
Alfieri, Salvatore
Romanò, Rebecca
Marceglia, Sara
Giorgi, Vincenzo De
Peris, Ketty
Sollena, Pietro
Piccerillo, Alfredo
Moro, Ruggero
Gualdi, Giulio
Ascierto, Paolo Antonio
Palla, Marco
Paone, Miriam
Eibenschutz, Laura
Spagnolo, Francesco
Queirolo, Paola
Filippini, Daria Maria
Cavalieri, Stefano
Resteghini, Carlo
Bergamini, Cristiana
Manocchio, Antonello
Source :
Oncologist; May2024, Vol. 29 Issue 5, pe699-e707, 9p
Publication Year :
2024

Abstract

Introduction In advanced basal cell carcinoma (BCC), the issue of whether Hedgehog inhibitors (HHIs) should be stopped or not after clinical complete response (cCR) achievement remains an unmet clinical need. Materials and Methods We conducted a retrospective, multicenter study across 7 Italian dermato-oncology units including patients with BCC who continued vismodegib after cCR between 2012 and 2019. We assessed the relationship between the duration of vismodegib intake (days to cCR [DTCR], days to stop after cCR [DTS], total treatment days [TTD]), and disease-free survival (DFS). Reasons to stop vismodegib were (R1) toxicity and (R2) disease recurrence. The relationship between DTCR, DTS, TTD, and DFS in the whole population and in R1 subgroup was assessed by Pearson's correlation coefficient (P  < .05) and Bayesian statistics (BF<subscript>10</subscript>). Results Sixty-eight BCC patients with a median (m) age of 75.5 years (39-100) were included. Most patients were male (N  = 43, 63%), without Gorlin syndrome (N  = 56, 82%) and with head and neck area as primary site (N  = 51, 75%). After cCR, out of 68 patients, 90% (N = 61/68) discontinued vismodegib: 82% (N  = 50/61) due to toxicity (R1), and 18% (N  = 11/61) due to recurrence (R2). Conversely, 10% (N  = 7/68) continued vismodegib until last follow-up. In the whole population (N  = 68), cCR was achieved with a mDTCR of 180.50 days. DFS showed a significant correlation with DTS (P  < .01, BF<subscript>10</subscript> = 39.2) and TTD (P  < .01, BF<subscript>10</subscript> = 35566), while it was not correlated to DTCR (BF<subscript>10</subscript> < 0.1). The analysis of R1 subgroup (N  = 50) confirmed these results. DFS correlated with DTS in all recurrent patients (N  = 38, r  = 0.44, P  < .01) and in the recurrent patients who stopped vismodegib for toxicity (N  = 26, r  = 0.665, P  < .01). DFS was longer when vismodegib was maintained for >2 months after cCR (mDFS > 2 months, N  = 54 vs. ≤ 2 months, N  = 14: 470 vs. 175 d, P  < .01). Conclusions Our retrospective results suggest that HHIs should be continued after cCR to improve DFS in BCC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10837159
Volume :
29
Issue :
5
Database :
Complementary Index
Journal :
Oncologist
Publication Type :
Academic Journal
Accession number :
177084414
Full Text :
https://doi.org/10.1093/oncolo/oyad319