Division of Hematology and Medical Oncology, Melvin and Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN.
Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, NC.
J Clin Oncol. 2020 Apr 20;38(12):1338-1345. doi: 10.1200/JCO.19.02569. Epub 2020 Mar 5.
Presence of teratoma in patients with metastatic testicular germ cell tumor (GCT) is of unknown prognostic significance. We report survival outcomes of patients with or without teratoma in primary tumor and postchemotherapy retroperitoneal lymph node dissection (PC-RPLND) specimen and assess impact on prognosis.
Patients with metastatic nonseminomatous GCT (NSGCT) who were evaluated at Indiana University between 1990 and 2016 and had primary testicular tumor specimen from orchiectomy (ORCH) were included. All patients were treated with cisplatin-based combination chemotherapy. The cohort was divided into 2 groups according to presence or absence of teratoma in ORCH specimen. Survival data were correlated with histopathologic findings. Differences in progression-free (PFS) and overall survival (OS) were evaluated using log-rank tests and Cox proportional hazards models to adjust for known adverse prognostic factors.
We identified 1,224 consecutive patients evaluated at Indiana University between 1990 and 2016 who met inclusion criteria. Median age was 27 years (range, 13-71 years); 689 patients had teratoma in ORCH specimen, and 535 did not. With median follow-up of 2.3 years, 5-year PFS was 61.9% (95% CI, 57.1% to 66.2%) for those with teratoma versus 63.1% (95% CI, 58.0% to 67.8%) for those without ( = .66); 5-year OS was 82.2% (95% CI, 77.9% to 85.8%) versus 81.4% (95% CI, 76.5% to 85.3%; = .91), respectively. A total of 473 patients underwent PC-RPLND; 5-year PFS for patients with pure teratoma in PC-RPLND specimen versus necrosis only was 65.9% versus 79.1% ( = .06), and 5-year OS was 90.3% versus 93.4% ( = .21), respectively.
Presence of teratoma in ORCH and PC-RPLND specimens was not a prognostic factor in this large retrospective study of patients with NSGCT.
在转移性睾丸生殖细胞肿瘤(GCT)患者中存在畸胎瘤的预后意义尚不清楚。我们报告了原发肿瘤和化疗后腹膜后淋巴结清扫术(PC-RPLND)标本中存在或不存在畸胎瘤的患者的生存结果,并评估了其对预后的影响。
纳入了 1990 年至 2016 年在印第安纳大学接受评估的转移性非精原细胞瘤性 GCT(NSGCT)患者,并对其睾丸切除术(ORCH)的原发睾丸肿瘤标本进行了分析。所有患者均接受顺铂为基础的联合化疗。根据 ORCH 标本中是否存在畸胎瘤,将队列分为 2 组。生存数据与组织病理学发现相关联。使用对数秩检验和 Cox 比例风险模型评估无进展生存期(PFS)和总生存期(OS)的差异,以调整已知的不良预后因素。
我们确定了 1990 年至 2016 年在印第安纳大学接受评估的 1224 例符合纳入标准的连续患者。中位年龄为 27 岁(范围,13-71 岁);689 例患者的 ORCH 标本中存在畸胎瘤,535 例患者不存在。中位随访 2.3 年后,有畸胎瘤的患者 5 年 PFS 为 61.9%(95%CI,57.1%-66.2%),无畸胎瘤的患者为 63.1%(95%CI,58.0%-67.8%)( =.66);5 年 OS 分别为 82.2%(95%CI,77.9%-85.8%)和 81.4%(95%CI,76.5%-85.3%)( =.91)。共有 473 例患者接受了 PC-RPLND;PC-RPLND 标本中单纯畸胎瘤患者与仅坏死患者的 5 年 PFS 分别为 65.9%和 79.1%( =.06),5 年 OS 分别为 90.3%和 93.4%( =.21)。
在这项对 NSGCT 患者的大型回顾性研究中,ORCH 和 PC-RPLND 标本中存在畸胎瘤并不是预后因素。