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Status: Bibliographieeintrag

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Verfasst von:Heppt, Markus V. [VerfasserIn]   i
 Gebhardt, Christoffer [VerfasserIn]   i
 Hassel, Jessica C. [VerfasserIn]   i
 Alter, Mareike [VerfasserIn]   i
 Gutzmer, Ralf [VerfasserIn]   i
 Leiter, Ulrike [VerfasserIn]   i
 Berking, Carola [VerfasserIn]   i
Titel:Long-term management of advanced basal cell carcinoma
Titelzusatz:current challenges and future perspectives
Verf.angabe:Markus V. Heppt, Christoffer Gebhardt, Jessica C. Hassel, Mareike Alter, Ralf Gutzmer, Ulrike Leiter and Carola Berking
E-Jahr:2022
Jahr:20 September 2022
Umfang:18 S.
Fussnoten:Gesehen am 11.01.2023
Titel Quelle:Enthalten in: Cancers
Ort Quelle:Basel : MDPI, 2009
Jahr Quelle:2022
Band/Heft Quelle:14(2022), 19, Artikel-ID 4547, Seite 1-18
ISSN Quelle:2072-6694
Abstract:The first-line therapy for locally advanced basal cell carcinoma (laBCC) is Hedgehog pathway inhibitors (HHIs), as they achieve good efficacy and duration of response. However, toxicity in the course of long-term treatment may lead to a decrease in the quality of life, and consequently to interruption or even discontinuation of therapy. As HHI therapy is a balancing act between effectiveness, adverse events, quality of life, and adherence, numerous successful treatment strategies have evolved, such as dose reduction and dose interruptions with on-off treatment schedules or interruptions with re-challenge after progression. As a small percentage of patients show primary or acquired resistance to HHIs, the inhibition of programmed cell death protein 1 (PD-1) has been approved as a second-line therapy, which may also be accompanied by immune-related toxicities and non-response. Thus, optimization of current treatment schedules, novel agents, and combination strategies are urgently needed for laBCC. Here, we narratively model the treatment sequence for patients with laBCC and summarize the current state of approved treatment regimens and therapeutic strategies to optimize the long-term management of laBCC.
DOI:doi:10.3390/cancers14194547
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.3390/cancers14194547
 Volltext: https://www.mdpi.com/2072-6694/14/19/4547
 DOI: https://doi.org/10.3390/cancers14194547
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:basal cell carcinoma
 Hedgehog pathway inhibitors
 immunotherapy
 programmed cell death protein 1 inhibitor
K10plus-PPN:1830800531
Verknüpfungen:→ Zeitschrift

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