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Synchronous Metastatic Clear-Cell Renal Cell Carcinoma: A Distinct Morphologic, Immunohistochemical, and Molecular Phenotype
- Source :
- Clinical Genitourinary Cancer, Clinical Genitourinary Cancer, 2017, 15 (1), pp.e1-e7. ⟨10.1016/j.clgc.2016.06.007⟩, Clinical Genitourinary Cancer, Elsevier, 2017, 15 (1), pp.e1-e7. 〈10.1016/j.clgc.2016.06.007〉, Clinical Genitourinary Cancer, Elsevier, 2017, 15 (1), pp.e1-e7. ⟨10.1016/j.clgc.2016.06.007⟩
- Publication Year :
- 2017
- Publisher :
- HAL CCSD, 2017.
-
Abstract
- International audience; INTRODUCTION: Clear cell renal cell carcinomas (ccRCCs) are highly metastatic tumors with metastases detected at diagnosis (synchronous) or during follow-up (metachronous). To date, there have been no reports comparing primary ccRCC of patients with synchronous and metachronous metastases, who are different in terms of prognosis. Determining whether there is a phenotypic difference between these 2 groups could have important clinical implications. PATIENTS AND METHODS: In a retrospective consecutive cohort of 98 patients with ccRCC, 48 patients had metastases, including 28 synchronous and 20 metachronous presentations, with a follow-up of 10 years. For each primary tumor in these metastatic patients, pathologic criteria, expression of vascular endothelial growth factor, partitioning-defective 3, CAIX, and programmed death ligand 1 as detected by immunohistochemistry, and complete VHL status were analyzed. Univariate analysis was performed, and survival was assessed using Kaplan-Meier curves compared by log-rank test. RESULTS: Compared with primary ccRCC in patients with metachronous metastases, primary ccRCC in patients with synchronous metastases were significantly associated with a poorer Eastern Cooperative Oncology Group performance (P = .045), higher pT status (P = .038), non-inactivated VHL gene (P = .01), sarcomatoid component (P = .007), expression of partitioning-defective 3 (P = .007), and overexpressions of vascular endothelial growth factor (> 50%) (P = .017) and programmed death ligand 1 (P = .019). Patients with synchronous metastases had a worse cancer-specific survival than patients with metachronous metastases even from metastatic diagnosis (median survival, 16 months vs. 46 months, respectively; P = .01). CONCLUSION: This long-term study is the first to support the notion that synchronous m-ccRCC has a distinct phenotype. This is probably linked to the occurrence of oncogenic events that could explain the worse prognosis. These particular patients with metastases could benefit from specific therapy.
- Subjects :
- Male
Vascular Endothelial Growth Factor A
0301 basic medicine
Oncology
Clear cell renal cell carcinoma
[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutrition
Cell
Cell Cycle Proteins
[SDV.MHEP.UN]Life Sciences [q-bio]/Human health and pathology/Urology and Nephrology
B7-H1 Antigen
[ SDV.CAN ] Life Sciences [q-bio]/Cancer
Neoplasms, Multiple Primary
chemistry.chemical_compound
0302 clinical medicine
Neoplasm Metastasis
Aged, 80 and over
Univariate analysis
Clinical outcome
Neoplasms, Second Primary
Middle Aged
[ SDV.MHEP.EM ] Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolism
Prognosis
Primary tumor
VEGF
Kidney Neoplasms
3. Good health
Gene Expression Regulation, Neoplastic
Vascular endothelial growth factor
medicine.anatomical_structure
Von Hippel-Lindau Tumor Suppressor Protein
030220 oncology & carcinogenesis
Cohort
Immunohistochemistry
Female
Adult
medicine.medical_specialty
Urology
[SDV.CAN]Life Sciences [q-bio]/Cancer
Diagnosis, Differential
03 medical and health sciences
Internal medicine
Biomarkers, Tumor
medicine
Humans
Carbonic Anhydrase IX
Carcinoma, Renal Cell
VHL gene
Adaptor Proteins, Signal Transducing
Aged
Retrospective Studies
business.industry
Genetic Variation
Membrane Proteins
Synchronous and metachronous metastases
medicine.disease
Survival Analysis
Sarcomatoid component
030104 developmental biology
chemistry
business
Clear cell
Subjects
Details
- Language :
- English
- ISSN :
- 15587673
- Database :
- OpenAIRE
- Journal :
- Clinical Genitourinary Cancer, Clinical Genitourinary Cancer, 2017, 15 (1), pp.e1-e7. ⟨10.1016/j.clgc.2016.06.007⟩, Clinical Genitourinary Cancer, Elsevier, 2017, 15 (1), pp.e1-e7. 〈10.1016/j.clgc.2016.06.007〉, Clinical Genitourinary Cancer, Elsevier, 2017, 15 (1), pp.e1-e7. ⟨10.1016/j.clgc.2016.06.007⟩
- Accession number :
- edsair.doi.dedup.....e330db4fd4084a4db24b664f6cf5d185