The clinical value of complete blood count-based immun parameter in predicting testicular cancer pathology and prognosis

Author:

Şimşekoğlu Muhammed Fatih1ORCID,Vural Ahmet1ORCID,Macit Mustafa2ORCID,Yıldız Fatih3ORCID,Kalender Göktuğ1ORCID,Aferin Uğur4ORCID,Gültekin Mehmet Hamza1ORCID,Demirdağ Çetin1ORCID

Affiliation:

1. İSTANBUL ÜNİVERSİTESİ-CERRAHPAŞA, CERRAHPAŞA TIP FAKÜLTESİ, CERRAHİ TIP BİLİMLERİ BÖLÜMÜ, ÜROLOJİ ANABİLİM DALI

2. İSTANBUL ÜNİVERSİTESİ, CERRAHPAŞA TIP FAKÜLTESİ, CERRAHİ TIP BİLİMLERİ BÖLÜMÜ, ÜROLOJİ ANABİLİM DALI

3. İSTANBUL ÜNİVERSİTESİ, CERRAHPAŞA TIP FAKÜLTESİ, CERRAHİ TIP BİLİMLERİ BÖLÜMÜ, ÜROLOJİ ANABİLİM DALI, ANDROLOJİ BİLİM DALI

4. Gayrettepe Grup Florence Nightingale Hastanesi

Abstract

Aim: The management of testicular cancer (TC) requires more specific and applicable biomarkers. We aimed to determine the ability of complete blood count (CBC) based inflammatory markers to predict tumor pathology and prognosis in TC. Methods: Patients who underwent inguinal orchiectomy for testicular germ cell tumors (TGCTs) at our hospital between January 2011 and December 2022 were included in the study. The medical records of patients with pathologically confirmed TC, including demographics, preoperative tumor markers, preoperative CBC, tumor characteristics, pathological outcomes, postoperative follow-up, and survival outcomes, were retrospectively collected. CBC-based inflammatory markers were compared between seminomatous and non-seminomatous TGCTs. To determine the independent prognostic significance of survival, the data were analyzed and fitted to the multivariate Cox proportional risk regression model. Results: The median follow-up was 48 (1-140) months. In our chord, 69 patients had seminomatous TGCTs (Group 1), and 66 had non-seminomatous TGCTs (Group 2). The median ages of Groups 1 and 2 were 35 (22-74) years and 31 (21-72) years(p

Publisher

Anadolu Klinigi Tip Bilimleri Dergisi

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