Molecular Characterization of Ovarian Yolk Sac Tumor (OYST).
OYST
molecular characteristics
patient outcome
targetable mutation
Journal
Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829
Informations de publication
Date de publication:
09 Jan 2021
09 Jan 2021
Historique:
received:
27
11
2020
revised:
30
12
2020
accepted:
07
01
2021
entrez:
13
1
2021
pubmed:
14
1
2021
medline:
14
1
2021
Statut:
epublish
Résumé
Most patients with malignant ovarian germ cell tumors (MOGTCs) have a very good prognosis and chemotherapy provides curative treatment; however, patients with yolk sac tumors (OYSTs) have a significantly worse prognosis. OYSTs are rare tumors and promising results are expected with the use of specific therapeutic strategies after the failure of platinum-based first-line and salvage regimens. We initiated a project in collaboration with EORTC SPECTA, to explore the molecular characteristics of OYSTs. The pilot project used retrospective samples from ten OYST relapsed and disease-free patients. Each patient had a molecular analysis performed with FoundationOne CDx describing the following variables according to the Foundation Medicine Incorporation (FMI): alteration type (SNV, deletion), actionable gene alteration, therapies approved in EU (for patient's tumor type and other tumor types), tumor mutational burden (TMB), and microsatellite instability (MSI) status. A total of 10 patients with OYST diagnosed between 2007 and 2017 had a molecular analysis. A molecular alteration was identified in four patients (40%). A subset of three patients (33.3% of all patients) harbored targetable oncogenic mutations in
Identifiants
pubmed: 33435376
pii: cancers13020220
doi: 10.3390/cancers13020220
pmc: PMC7826864
pii:
doi:
Types de publication
Journal Article
Langues
eng
Références
Nat Rev Cancer. 2011 Oct 13;11(11):761-74
pubmed: 21993244
Am J Cancer Res. 2012;2(2):153-67
pubmed: 22432056
Int J Gynecol Cancer. 2011 Nov;21(8):1414-21
pubmed: 21795985
Gynecol Oncol. 2017 Nov;147(2):296-301
pubmed: 28803748
Crit Rev Oncol Hematol. 2019 Nov;143:130-138
pubmed: 31634730
Lancet Oncol. 2010 Jul;11(7):685-93
pubmed: 20362508
Sci Transl Med. 2017 Nov 1;9(414):
pubmed: 29093181
Ann Oncol. 2017 Jun 1;28(6):1274-1279
pubmed: 28398524
Am J Clin Oncol. 2006 Feb;29(1):12-3
pubmed: 16462496
Cancer. 2011 May 15;117(10):2096-103
pubmed: 21523721
Expert Opin Investig Drugs. 2016 Sep;25(9):1033-43
pubmed: 27286362
Lancet Oncol. 2007 Nov;8(11):1039-40
pubmed: 17976614
Mol Cancer Ther. 2009 Apr;8(4):834-43
pubmed: 19372556
Clin Cancer Res. 2019 Sep 15;25(18):5584-5594
pubmed: 31196855
J Clin Oncol. 2008 Nov 20;26(33):5352-9
pubmed: 18955458
Endocr Rev. 2013 Jun;34(3):339-76
pubmed: 23575763
Mol Cancer. 2007 Feb 02;6:12
pubmed: 17274819
Oncoimmunology. 2017 Mar 20;6(4):e1305535
pubmed: 28507813
Eur J Cancer. 2011 Nov;47(17):2493-511
pubmed: 22033323
BMC Med. 2011 Aug 26;9:99
pubmed: 21867560
Proc Natl Acad Sci U S A. 2009 Feb 3;106(5):1542-7
pubmed: 19164557
Ann Oncol. 2018 Jan 1;29(1):209-214
pubmed: 29045540
Cancer Discov. 2015 Jul;5(7):752-67
pubmed: 26069190
Invest New Drugs. 2019 Aug;37(4):748-754
pubmed: 31152292
Nat Rev Cancer. 2011 Nov 17;11(12):865-78
pubmed: 22089421
J Pathol. 2006 Feb;208(3):395-400
pubmed: 16273510
Cancers (Basel). 2019 Oct 11;11(10):
pubmed: 31614500
J Clin Oncol. 2019 Sep 20;37(27):2406-2415
pubmed: 31403866
Eur J Surg Oncol. 2019 Jan;45(1):67-74
pubmed: 29108961