Comparison of the biomarkers for targeted therapies in primary extra-mammary and mammary Paget's disease
Language English Country United States Media print-electronic
Document type Comparative Study, Journal Article
PubMed
31899853
PubMed Central
PMC7013075
DOI
10.1002/cam4.2820
Knihovny.cz E-resources
- Keywords
- extra-mammary Paget's disease, immune therapy, molecular profiling, targeted therapy,
- MeSH
- Gene Amplification MeSH
- Molecular Targeted Therapy MeSH
- Adult MeSH
- Paget Disease, Extramammary drug therapy genetics pathology MeSH
- Precision Medicine MeSH
- Skin pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Microsatellite Instability MeSH
- Mutation MeSH
- Biomarkers, Tumor antagonists & inhibitors genetics metabolism MeSH
- Skin Neoplasms drug therapy genetics pathology MeSH
- Breast Neoplasms drug therapy genetics pathology MeSH
- Paget's Disease, Mammary drug therapy genetics pathology MeSH
- Antineoplastic Combined Chemotherapy Protocols pharmacology therapeutic use MeSH
- Breast pathology MeSH
- Retrospective Studies MeSH
- Sequence Analysis, DNA MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Scrotum pathology MeSH
- DNA Copy Number Variations MeSH
- Vulva pathology MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
- Names of Substances
- Biomarkers, Tumor MeSH
BACKGROUND: Primary Extra-mammary Paget's disease (EMPD) is a very rare cutaneous adenocarcinoma affecting anogenital or axillary regions. It is characterized by a prolonged course with recurrences and eventually distant metastatic spread for which no specific therapy is known. METHODS: Eighteen EMPD (13 vulvar and five scrotal) and ten mammary Paget's disease (MPD) cases were comprehensively profiled for gene mutations, fusions and copy number alterations, and for therapy-relevant protein biomarkers). RESULTS: Mutations in TP53 and PIK3CA were the most frequent in both cohorts: 7/15 and 5/15 in EMPD; 1/6 and 4/7 in MPD HER2 gene amplification was detected in 4/18 EMPD (3 vulvar and 1 scrotal case) in contrast to MPD where it was detected in the majority (7/8) of cases. TOP2A gene amplification was seen in 2/12 EMPD and 1/6 MPD, respectively. Similarly, no difference in estrogen receptor expression was seen between the EMPD (4/15) and MPD (3/10). Androgen receptor was also expressed in the majority of both cohorts (12/16 EMPD) and (7/8 MPD).Here ARv7 splice variant was detected in 1/7 EMPD and 1/4 MPD cases, respectively. PD-L1 expression on immune cells was exclusively observed in three vulvar EMPD. In contrast to MPD, six EMPDs harbored a "high" tumor mutation burden (≥10 mutations/Mb). All tested cases from both cohorts were MSI stable. CONCLUSIONS: EMPD shares some targetable biomarkers with its mammary counterpart (steroid receptors, PIK3CA signaling pathways, TOP2A amplification). HER2 positivity is notably lower in EMPD while biomarkers to immune checkpoint inhibitors (high TMB and PD-L1) were observed in some EMPD. Given that no consistent molecular alteration characterizes EMPD, comprehensive theranostic profiling is required to identify individual patients with targetable molecular alterations.
Bioptical Laboratory Pilsen Czech Republic
Caris Life Sciences Phoenix AZ USA
College of Medicine QU Health Qatar University Doha Qatar
Gustave Roussy Cancer Center INSERM U981 Paris France
Norris Comprehensive Cancer Center University of Southern California Los Angeles CA USA
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