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During twenty years of Cisplatin-based therapy the face of nonseminomatous testicular germ cell tumors is still changing: an evaluation of presentation, management, predictive factors and survival
International Braz J Urol; Heinzelbecker, Julia; Katzmarzik, Michaela; Weiss, Christel; Trojan, Lutz; Haecker, Axel.
  • Heinzelbecker, Julia; University of Heidelberg. Medical Faculty Mannheim. University Medical Center Mannheim. Department of Urology. Mannheim. DE
  • Katzmarzik, Michaela; University of Heidelberg. Medical Faculty Mannheim. University Medical Center Mannheim. Department of Urology. Mannheim. DE
  • Weiss, Christel; University of Heidelberg. Medical Faculty Mannheim. University Medical Center Mannheim. Department of Urology. Mannheim. DE
  • Trojan, Lutz; University of Heidelberg. Medical Faculty Mannheim. University Medical Center Mannheim. Department of Urology. Mannheim. DE
  • Haecker, Axel; University of Heidelberg. Medical Faculty Mannheim. University Medical Center Mannheim. Department of Urology. Mannheim. DE
Int. braz. j. urol ; 39(1): 10-21, January-February/2013. tab, graf
Article in English | LILACS | ID: lil-670376
ABSTRACT

Purpose:

To assess the changing presentation and treatment of nonseminomatous testicular germ cell tumors (NSGCT) and to investigate predictive factors for the status of metastasis at diagnosis and on relapse and death. Materials and

Methods:

Retrospective record review of 147 patients that underwent inguinal orchiectomy from 1987-2007. Follow-up data was available for 102 patients (median follow-up 80 months (0-243); 96 patients alive).

Results:

Mean patients age increased (p = 0.015) and more patients were diagnosed in clinical stage I (CSI) (p = 0.040). The fraction of yolk sac (YS) elements inclined (p = 0.030) and pT2 tumors increased (p < 0.001). Retroperitoneal lymph node dissection (RPLND) declined whereas more patients were treated with chemotherapy (p < 0.001; p = 0.004). There was an increase in relapse free (RFS) and cancer specific survival (CSS) due to an improvement in patients with disseminated disease (p = 0.014; p < 0.001). The presence of YS and teratoma elements showed a reduction in the odds ratio (OR) for metastasis at diagnosis (p = 0.002, OR 0.262; p = 0.009, OR 0.428) whereas higher pT-stage was associated to their presence (p = 0.039). Patients with disseminated disease (CS > I) showed a declined CSS compared to CSI patients (p = 0.055). The presence of YS elements was associated to an improved RFS (p = 0.038).

Conclusions:

In our single institution study the face of NSGCT markedly changed over 20 years even after the introduction of Cisplatin-based chemotherapy. These changes were accompanied by an improvement in RFS and CSS. When dealing with NSGCT patients such observations now and in the future should be taken into account. .
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Testicular Neoplasms / Cisplatin / Neoplasms, Germ Cell and Embryonal / Antineoplastic Agents Type of study: Etiology study / Observational study / Prognostic study Limits: Humans / Male Language: English Journal: Int. braz. j. urol Journal subject: Urology Year: 2013 Type: Article Affiliation country: Germany Institution/Affiliation country: University of Heidelberg/DE

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Full text: Available Index: LILACS (Americas) Main subject: Testicular Neoplasms / Cisplatin / Neoplasms, Germ Cell and Embryonal / Antineoplastic Agents Type of study: Etiology study / Observational study / Prognostic study Limits: Humans / Male Language: English Journal: Int. braz. j. urol Journal subject: Urology Year: 2013 Type: Article Affiliation country: Germany Institution/Affiliation country: University of Heidelberg/DE