Schneider Dominik T, Orbach Daniel, Cecchetto Giovanni, Stachowicz-Stencel Teresa, Brummel Bastian, Brecht Ines B, Bisogno Gianni, Ferrari Andrea, Reguerre Yves, Godzinski Jan, Bien Ewa, Calaminus Gabriele, Göbel Ulrich, Patte Catherine
Clinic of Pediatrics, Beurhausstr. 40, D-44137 Dortmund, Germany.
Department of Paediatric Oncology, Institut Curie, 26 rue d'Ulm, Paris 75231, France.
Eur J Cancer. 2015 Mar;51(4):543-550. doi: 10.1016/j.ejca.2014.11.013. Epub 2014 Dec 13.
To analyse ovarian Sertoli-Leydig cell tumours (SLCTs) for potential prognostic markers and their use for treatment stratification.
Forty-four patients were included. Patients were prospectively reported to the German MAKEI (Maligne Keimzelltumoren) studies (n=23), French TGM protocols (n=10), Italian Rare Tumour Project (TREP) registry (n=6), and the Polish Pediatric Rare Tumour Study group (n=5). Tumours were classified according to World Health Organisation (WHO) and staged according to International Federation of Gynecological Oncology (FIGO).
Median age was 13.9 (0.5-17.4) years. All patients underwent resection by tumour enucleation (n=8), ovariectomy (n=17), adenectomy isolated (n=18) or with hysterectomy (n=1). FIGO-stage: Ia 24pts., Ic 17pts., II/III 3pts. One patient had bilateral tumours. Four patients (stage Ia: 3, stage Ic: 1) developed a metachronous contralateral tumour. Otherwise, all stage Ia patients remained in complete remission. Among 20 patients with incomplete resection or tumour spread (stage Ic-III), eight relapsed, and five patients died. Eleven patients were initially treated with two to sixcycles of cisplatin-based chemotherapy. Of these, seven patients are in continuous remission. Poor histological differentiation was associated with higher relapse rate (5/13) compared to intermediate (3/18) and high differentiation (0/4). Tumours with retiform pattern or heterologous elements showed a high relapse rate, too (5/11). After a median follow-up of 62 months, event-free survival is 0.70±0.07, relapse-free survival 0.81±0.06 and overall survival 0.87±0.05.
Prognosis of SLCTs is determined by stage and histopathologic differentiation. Complete resection with careful avoidance of spillage is a prerequisite of cure. The impact of chemotherapy in incompletely resected and advanced stage tumours remains to be evaluated.
分析卵巢支持-间质细胞瘤(SLCTs)的潜在预后标志物及其在治疗分层中的应用。
纳入44例患者。前瞻性报告的患者来自德国MAKEI(恶性生殖细胞肿瘤)研究(n = 23)、法国TGM方案(n = 10)、意大利罕见肿瘤项目(TREP)登记处(n = 6)以及波兰儿童罕见肿瘤研究组(n = 5)。肿瘤根据世界卫生组织(WHO)进行分类,并根据国际妇产科联盟(FIGO)进行分期。
中位年龄为13.9(0.5 - 17.4)岁。所有患者均接受了肿瘤剜除术(n = 8)、卵巢切除术(n = 17)、孤立性腺切除术(n = 18)或联合子宫切除术(n = 1)。FIGO分期:Ia期24例,Ic期17例,II/III期3例。1例患者为双侧肿瘤。4例患者(Ia期:3例,Ic期:1例)出现异时性对侧肿瘤。除此之外,所有Ia期患者均保持完全缓解。在20例不完全切除或肿瘤播散(Ic - III期)的患者中,8例复发,5例死亡。11例患者最初接受了2至6周期以顺铂为基础的化疗。其中,7例患者持续缓解。与中分化(3/18)和高分化(0/4)相比,低组织学分化与更高的复发率相关(5/13)。具有网状结构或异源性成分的肿瘤也显示出较高复发率(5/11)。中位随访62个月后,无事件生存率为0.70±0.07,无复发生存率为0.81±0.06,总生存率为0.87±0.05。
SLCTs的预后由分期和组织病理学分化决定。彻底切除并小心避免肿瘤溢出是治愈的前提。化疗在不完全切除和晚期肿瘤中的作用仍有待评估。