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Titel: Reinduction of Hedgehog Inhibitors after Checkpoint Inhibition in Advanced Basal Cell Carcinoma : A Series of 12 Patients
VerfasserIn: DeTemple, Viola K.
Hassel, Jessica C.
Sachse, Michael M.
Grimmelmann, Imke
Leiter, Ulrike
Gebhardt, Christoffer
Eckardt, Julia
Pföhler, Claudia
Angela, Yenny
Hübbe, Hanna
Gutzmer, Ralf
Sprache: Englisch
Titel: Cancers
Bandnummer: 14
Heft: 21
Verlag/Plattform: MDPI
Erscheinungsjahr: 2022
Freie Schlagwörter: advanced basal cell carcinoma
hedgehog inhibitor reinduction
sequential treatment
checkpoint inhibition
DDC-Sachgruppe: 610 Medizin, Gesundheit
Dokumenttyp: Journalartikel / Zeitschriftenartikel
Abstract: For patients with advanced basal cell carcinoma (aBCC) first-line treatment with hedgehog inhibitors (HHIs) and second-line treatment with PD1 inhibitors (PD1i) is available, offering combination and sequencing options. Here, we focus on the efficacy and safety of HHI reinduction after PD1i failure. Retrospective data analysis was performed with 12 patients with aBCC (locally advanced (n = 8)/metastatic (n = 4)). These patients (male:female 6:6, median age 68 years) initially received HHIs, leading to complete/partial response (66%) or stable disease (33%). Median treatment duration was 20.8 (2–64.5) months until discontinuation due to progression (n = 8), adverse events (n = 3), or patient request (n = 1). Subsequent PD1 inhibition (pembrolizumab 42%, cemiplimab 58%) yielded a partial response (8%), stable disease (33%), or progression (59%). Median treatment duration was 4.1 (0.8–16.3) months until discontinuation due to progression (n = 9), adverse events (n = 1), patient request (n = 1), or missing drug approval (n = 1). HHI reinduction resulted in complete/partial response (33%), stable disease (50%), or progression (17%). Median treatment duration was 3.6 (1–29) months. Response duration in the four responding patients was 2–29+ months. Thus, a subgroup of patients with aBCC responded to reinduction of HHI following PD1i failure. Therefore, this sequential treatment represents a feasible treatment option.
DOI der Erstveröffentlichung: 10.3390/cancers14215469
Link zu diesem Datensatz: urn:nbn:de:bsz:291--ds-379428
hdl:20.500.11880/34297
http://dx.doi.org/10.22028/D291-37942
ISSN: 2072-6694
Datum des Eintrags: 11-Nov-2022
Fakultät: M - Medizinische Fakultät
Fachrichtung: M - Dermatologie
Professur: M - Keiner Professur zugeordnet
Sammlung:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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