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Malignancy after Augmentation Enterocystoplasty: A Nationwide Study of Natural History, Prognosis and Oncogene Panel Analysis
- Source :
- Journal of Urology, Journal of Urology, Elsevier, 2020, 204 (1), pp.136-143. ⟨10.1097/JU.0000000000000752⟩
- Publication Year :
- 2020
-
Abstract
- International audience; We report the natural history and prognosis of tumors after augmentation enterocystoplasty, with a molecular analysis using an oncogene panel to search for potential targeted therapies.Materials and methods: this multicenter, nationwide, retrospective study included 16 patients. A panel of 21 clinically relevant oncogenes was tested on archival tumor specimens using next-generation sequencing. Survival rate was the main clinical outcome and sequences were compared to the reference genome for the genetic outcome.Results: augmentation enterocystoplasties were performed mainly for congenital neurogenic bladder and bladder exstrophy at a median patient age of 17 years (range 4 months to 45 years). Most of the malignancies were diagnosed because of clinical manifestations, with a median latency period of 20 years. Adenocarcinomas were mainly found after gastrocystoplasty, whereas urothelial cell carcinomas were typically found after colocystoplasty. Of the 16 patients 13 were diagnosed at an advanced stage of the disease (positive lymph nodes in 7, distant metastases in 6). The overall 1-year survival rate was 56%. Only 3 patients remained disease-free at a median followup of 70 months. Of the 9 tumors with analyzable DNA 4 were wild-type and 5 harbored missense mutations (KIT-p.Pro573Ser, PDGFRA-p.Glu587Lys, KRAS-p.Gly12Asp, ERBB4p.Arg484Lys, CTNNB1-p.Ser37Phe and p.Ser47Asn).Conclusions: malignancy after augmentation enterocystoplasty is diagnosed late with frequent metastases and a very low 1-year survival rate. More than half the tested samples harbored missense mutations in oncogenes accessible to targeted therapies. An international collaboration to enlarge the genetic panel analysis of these tumors may offer new therapeutic hope to patients.
- Subjects :
- Oncology
Male
MESH: Oncogenes
DNA Mutational Analysis
030232 urology & nephrology
[SDV.MHEP.UN]Life Sciences [q-bio]/Human health and pathology/Urology and Nephrology
0302 clinical medicine
Neoplasms
MESH: Urinary Bladder
MESH: Child
MESH: DNA Mutational Analysis
Neoplasm Metastasis
Child
MESH: High-Throughput Nucleotide Sequencing
MESH: Urologic Surgical Procedures
High-Throughput Nucleotide Sequencing
Prognosis
3. Good health
Molecular analysis
MESH: Urinary Bladder Neoplasms
Natural history
Survival Rate
MESH: Young Adult
030220 oncology & carcinogenesis
Urologic Surgical Procedures
Female
France
Adult
medicine.medical_specialty
MESH: Urinary Bladder, Neurogenic
MESH: Survival Rate
Adolescent
Urology
Urinary Bladder
Mutation, Missense
[SDV.CAN]Life Sciences [q-bio]/Cancer
Adenocarcinoma
Malignancy
MESH: Prognosis
03 medical and health sciences
Young Adult
MESH: Bladder Exstrophy
Internal medicine
medicine
Genetics
Humans
Urinary Bladder, Neurogenic
Retrospective Studies
MESH: Adolescent
MESH: Carcinoma, Transitional Cell
MESH: Mutation, Missense
Carcinoma, Transitional Cell
MESH: Humans
Oncogene
business.industry
MESH: Adenocarcinoma
Bladder Exstrophy
MESH: Retrospective Studies
MESH: Adult
Oncogenes
medicine.disease
MESH: Neoplasm Metastasis
MESH: Male
Bladder exstrophy
MESH: France
Panel analysis
Urinary Bladder Neoplasms
business
MESH: Female
Subjects
Details
- ISSN :
- 15273792 and 00225347
- Volume :
- 204
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- The Journal of urology
- Accession number :
- edsair.doi.dedup.....d376c94c3c6ddef0e89398e5fb91d894
- Full Text :
- https://doi.org/10.1097/JU.0000000000000752⟩