TY - JOUR
T1 - Safety and efficacy of nivolumab, an anti-PD1 immunotherapy, in patients with advanced basal cell carcinoma, after failure or intolerance to sonic Hedgehog inhibitors
T2 - UNICANCER AcSé NIVOLUMAB trial
AU - Véron, Marie
AU - Chevret, Sylvie
AU - Grob, Jean Jacques
AU - Beylot-Barry, Marie
AU - Saiag, Philippe
AU - Fléchon, Aude
AU - You, Benoit
AU - Maubec, Eve
AU - Jouary, Thomas
AU - Toulemonde, Elise
AU - Jamme, Philippe
AU - Gambotti, Laëtitia
AU - Lamrani-Ghaouti, Assia
AU - Dupuy, Alain
AU - Lebbe, Céleste
AU - Seguin, Nicole Basset
AU - Houede, Nadine
AU - Leccia, Marie Thérèse
AU - Le Du, Fanny
AU - de Pontville, Michel
AU - Gaudy-Marquestre, Caroline
AU - Guillot, Bernard
AU - Simon, Clotilde
AU - Marabelle, Aurélien
AU - Mortier, Laurent
N1 - Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Background: Basal cell carcinoma (BCC) is the most common human malignancy. In most cases, BCC has slow progression and can be definitively cured by surgery or radiotherapy. However, in rare cases, it can become locally advanced or, even more rarely, metastatic. The alternative recommended treatments are Sonic Hedgehog pathway inhibitors; however, the response is often short-lived. Methods: This was a phase 2 basket study (NCT03012581) evaluating the efficacy and safety of nivolumab in a cohort of 32 advanced BCC patients, enrolled after failure of Sonic Hedgehog inhibitors, including 29 laBCC (91%) and 3 mBCC (9%). Results: Compared to previously published studies, our population consisted of severe patients with a poor prognosis because they had already received multiple lines of treatment: all patients received previous Sonic Hedgehog inhibitors, 53% of patients already had chemotherapy and 75% radiotherapy. At 12 weeks, we reported 3.1% of complete responses, 18.8% of partial responses, and 43.8% of stable diseases. The best response rate to nivolumab reached 12.5% of complete responses (four patients), 18.8% of partial responses (three patients), and 43.8% of stable diseases (14 patients). Adverse events (AE) were mostly grade 2 or 3, slightly different to the adverse events observed in the treatment of metastatic melanoma (higher rate of diabetes, no thyroid dysfunction). Conclusion: Nivolumab is a relevant therapeutic option for patients with advanced relapsing/refractory BCC.
AB - Background: Basal cell carcinoma (BCC) is the most common human malignancy. In most cases, BCC has slow progression and can be definitively cured by surgery or radiotherapy. However, in rare cases, it can become locally advanced or, even more rarely, metastatic. The alternative recommended treatments are Sonic Hedgehog pathway inhibitors; however, the response is often short-lived. Methods: This was a phase 2 basket study (NCT03012581) evaluating the efficacy and safety of nivolumab in a cohort of 32 advanced BCC patients, enrolled after failure of Sonic Hedgehog inhibitors, including 29 laBCC (91%) and 3 mBCC (9%). Results: Compared to previously published studies, our population consisted of severe patients with a poor prognosis because they had already received multiple lines of treatment: all patients received previous Sonic Hedgehog inhibitors, 53% of patients already had chemotherapy and 75% radiotherapy. At 12 weeks, we reported 3.1% of complete responses, 18.8% of partial responses, and 43.8% of stable diseases. The best response rate to nivolumab reached 12.5% of complete responses (four patients), 18.8% of partial responses (three patients), and 43.8% of stable diseases (14 patients). Adverse events (AE) were mostly grade 2 or 3, slightly different to the adverse events observed in the treatment of metastatic melanoma (higher rate of diabetes, no thyroid dysfunction). Conclusion: Nivolumab is a relevant therapeutic option for patients with advanced relapsing/refractory BCC.
KW - Basal cell carcinoma
KW - Cancer
KW - Immune checkpoint
KW - Immunotherapy
KW - Locally advanced basal cell carcinoma
KW - Metastatic basal cell carcinoma
KW - Nivolumab
KW - PD1 blocker
UR - http://www.scopus.com/inward/record.url?scp=85141293974&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2022.09.013
DO - 10.1016/j.ejca.2022.09.013
M3 - Article
C2 - 36335780
AN - SCOPUS:85141293974
SN - 0959-8049
VL - 177
SP - 103
EP - 111
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -