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Prognostic factors and treatment impact on overall survival in patients with renal neuroendocrine tumour.
Omidele, Olamide O; Connors, Christopher; Wainganker, Nikhil; Badani, Ketan; Sfakianos, John; Mehrazin, Reza; Jayaratna, Isuru.
Affiliation
  • Omidele OO; Department of Urology Icahn School of Medicine at Mount Sinai New York New York USA.
  • Connors C; Department of Urology Icahn School of Medicine at Mount Sinai New York New York USA.
  • Wainganker N; Department of Urology Icahn School of Medicine at Mount Sinai New York New York USA.
  • Badani K; Department of Urology Icahn School of Medicine at Mount Sinai New York New York USA.
  • Sfakianos J; Department of Urology Icahn School of Medicine at Mount Sinai New York New York USA.
  • Mehrazin R; Department of Urology Icahn School of Medicine at Mount Sinai New York New York USA.
  • Jayaratna I; Department of Urology Icahn School of Medicine at Mount Sinai New York New York USA.
BJUI Compass ; 5(6): 576-584, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38873350
ABSTRACT

Background:

Renal neuroendocrine neoplasms (R-NEN) are exceptionally rare tumours characterized by high mortality rates.

Objective:

The objective of this study is to analyse prognostic factors and treatment impact on overall survival in patients with R-NEN. Design setting and

participants:

We identified all patients with R-NEN in the National Cancer Database (NCDB) from 2004 to 2019 and identified prognostic factors for improved survival. Results and

limitations:

Of 542 R-NEN cases, 166 (31%) were neuroendocrine tumour grade 1 (NET-G1), 14 (3%) were neuroendocrine tumour grade 2 (NET-G2), 169 (31%) were neuroendocrine carcinoma (NEC-NOS), 18 (3%) were large cell neuroendocrine carcinoma (LC-NEC) and 175 (32%) were small cell neuroendocrine carcinoma (SC-NEC). Median overall survival for all patients in the study was 44.88 months (SE, 4.265; 95% CI, 27.57-62.19). Median overall survival was 7.89 months (SE 0.67; 95% CI, 6.58-9.20) for patients without surgical intervention and 136.61 months (SE 16.44; 95% CI, 104.38-168.84, p < 0.001) for patients who underwent surgery. Increased age (HR, 1.05; 95% CI, 1.03-1.06; p < 0.001), T4 stage disease (HR, 3.17; 95% CI, 1.96-5.1; p < 0.001), NEC-NOS histology (HR, 2.82; 95% CI, 1.64-4.86; p < 0.001), LC-NEC histology (HR, 2.73; 95% CI, 1.04-7.17; p = 0.041) and SC-NEC histology (HR, 5.17; 95% CI, 2.95-9.05; p < 0.001) were all positive predictors of worsening overall survival. The main limitation of the study is its retrospective design.

Conclusion:

R-NEN is an aggressive tumour characterized by high mortality rates. Surgery continues to be the mainstay of treatment and has shown to provide a survival benefit for most patients. Patient

Summary:

R-NEN is composed of several tumour histologies that differ based on their aggressiveness with NEC-NOS and SC-NEC being the most lethal. Surgery, predominantly through minimally invasive approaches, is the mainstay of treatment and has a clear survival benefit.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BJUI Compass Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BJUI Compass Year: 2024 Type: Article