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논문 기본 정보

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학술저널
저자정보
Kasumi Yoshinaga (Okayama University Graduate School of Medicine) Takuya Sadahira (Okayama University Graduate School of Medicine) Yuki Maruyama (Okayama University Graduate School of Medicine) Yosuke Mitsui (Okayama University Graduate School of Medicine) Takehiro Iwata (Okayama University Graduate School of Medicine) Koichiro Wada (Okayama University Graduate School of Medicine) Motoo Araki (Okayama University Graduate School of Medicine) Toyohiko Watanabe (Okayama University Graduate School of Medicine) Yasutomo Nasu (Okayama University Graduate School of Medicine)
저널정보
대한비뇨기과학회 Investigative and Clinical Urology Investigative and Clinical Urology Vol.62 No.1
발행연도
2021.1
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47 - 55 (9page)

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Purpose: The aim of this study was to compare the prognostic value of pretreatment inflammation-based scoring systems in terms of overall survival (OS) and progression-free survival (PFS) in patients with germ cell tumors (GCTs) receiving bleomycin, etoposide, and cisplatin (BEP) chemotherapy. Materials and Methods: We evaluated 63 patients with GCTs retrospectively. The Glasgow prognostic score (GPS), neutrophil-to-lymphocyte ratio, prognostic index, platelet-to-lymphocyte ratio (PLR), prognostic nutritional index (PNI), systemic immune-inflammation index, and albumin-to-globulin ratio (AGR) were measured in all patients before chemotherapy. To assess the predictive ability of each scoring system, areas under the receiver operating characteristic curve were calculated, and multivariate analysis was performed to identify associations between the predictive scores and OS. Results: Of all the inflammation-based scoring systems, the GPS had the greatest area under the curve (0.847) for predicting OS, followed by the PNI (0.829) and AGR (0.810). Kaplan–Meier analyses revealed that the GPS, PNI, and AGR were significantly associated with OS, whereas the GPS, PLR, and PNI were significantly associated with PFS. In the multivariate analysis, the GPS was an independent predictor of OS and PFS. Conclusions: We demonstrated that the GPS was the most valuable biomarker of OS and PFS in patients with GCTs.

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