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Naslov:BAP1-defficient breast cancer in a patient with BAP1 cancer syndrome
Avtorji:ID Blatnik, Ana (Avtor)
ID Ribnikar, Domen (Avtor)
ID Šetrajčič Dragoš, Vita (Avtor)
ID Novaković, Srdjan (Avtor)
ID Stegel, Vida (Avtor)
ID Grčar-Kuzmanov, Biljana (Avtor)
ID Boc, Nina (Avtor)
ID Perić, Barbara (Avtor)
ID Škerl, Petra (Avtor)
ID Klančar, Gašper (Avtor)
ID Krajc, Mateja (Avtor)
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (1,12 MB)
MD5: E522C712A5F7E5EC886C5E2CD9634B5E
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo OI - Onkološki inštitut Ljubljana
Povzetek:BAP1 cancer syndrome is a rare and highly penetrant hereditary cancer predisposition. Uveal melanoma, mesothelioma, renal cell carcinoma (RCC) and cutaneous melanoma are considered BAP1 cancer syndrome core cancers, whereas association with breast cancer has previously been suggested but not confirmed so far. In view of BAP1 immunomodulatory functions, BAP1 alterations could prove useful as possible biomarkers of response to immunotherapy in patients with BAP1-associated cancers. We present a case of a patient with BAP1 cancer syndrome who developed a metastatic breast cancer with loss of BAP1 demonstrated on immunohistochemistry. She carried a germline BAP1 likely pathogenic variant (c.898_899delAG p.(Arg300Glyfs*6)). In addition, tumor tissue sequencing identified a concurrent somatic variant in BAP1 (partial deletion of exon 12) and a low tumor mutational burden. As her triple negative tumor was shown to be PD-L1 positive, the patient was treated with combination of atezolizumab and nab-paclitaxel. She had a complete and sustained response to immunotherapy even after discontinuation of nab-paclitaxel. This case strengthens the evidence for including breast cancer in the BAP1 cancer syndrome tumor spectrum with implications for future cancer prevention programs. It also indicates immune checkpoint inhibitors might prove to be an effective treatment for BAP1-deficient breast cancer.
Ključne besede:BAP1, breast cancer, hereditary cancer syndromes, immunotherapy
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Datum objave:05.04.2022
Založnik:Springer
Leto izida:2022
Št. strani:str. 921–927
Številčenje:Vol. 29
PID:20.500.12556/DiRROS-15559 Novo okno
UDK:618.1
ISSN pri članku:1340-6868
DOI:10.1007/s12282-022-01354-0 Novo okno
COBISS.SI-ID:104001539 Novo okno
Avtorske pravice:by Authors
Datum objave v DiRROS:19.09.2022
Število ogledov:448
Število prenosov:180
Metapodatki:XML RDF-CHPDL DC-XML DC-RDF
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Gradivo je del revije

Naslov:Breast cancer
Skrajšan naslov:Breast cancer
Založnik:Japanese Breast Cancer Society
ISSN:1340-6868
COBISS.SI-ID:514824473 Novo okno

Gradivo je financirano iz projekta

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P3-0289-2019
Naslov:Značilnosti malignih neoplazem, pomembne za diagnozo ter napoved poteka bolezni in izida zdravljenja

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P3-0352-2018
Naslov:Družine s povišano ali visoko ogroženostjo za raka: svetovanje, odkrivanje mutacij in preprečevanje raka

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:17.09.2022

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:BAP1, rak dojke, dedni raki, imunoterapija


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