Indiana University School of Medicine, Indianapolis, IN.
Indiana University School of Medicine, Indianapolis, IN.
Urol Oncol. 2020 Aug;38(8):687.e19-687.e23. doi: 10.1016/j.urolonc.2020.04.024. Epub 2020 May 21.
Choriocarcinoma germ cell tumors are rare and usually present with significantly elevated human chorionic gonadotropin (hCG) levels. When curable, it is felt to be largely a result of chemotherapy. We sought to determine the histologic characteristics for those undergoing postchemotherapy retroperitoneal lymph node dissection (PC-RPLND) and compare them with metastatic nonseminomatous germ cell tumor (NSGCT) patients with similarly elevated hCG levels.
We reviewed medical records of men undergoing PC-RPLND between 1988 and 2017 with postorchiectomy, preinduction chemotherapy hCG levels greater than 50,000 mIU/ml. They were stratified by primary tumor histology: Pure choriocarcinoma and mixed NSGCT. Clinical, pathologic, and serologic data were reported and logistic regression was used to assess for predictors of necrosis in the PC-RPLND specimen.
Our cohort consisted of 108 men. The mixed group (n = 91) had a median hCG of 165,177 mIU/ml, a postchemotherapy node size of 4.7 cm, of whom 19.8% also received salvage chemotherapy prior to RPLND. The pure choriocarcinoma group (n = 17) had a median hCG of 170,267 mIU/ml, a node size of 5.1 cm, of whom 17.6% received salvage chemotherapy. 88.2% of patients with choriocarcinoma had necrosis in the PC-RPLND specimen compared with 29.7% of the mixed NSGCT group (P = <0.0001). Controlling for salvage chemotherapy use, prechemotherapy hCG, node size and marker status, choriocarcinoma patients were 20 fold more likely to have necrosis on RPLND specimen (Odds ratio 20.68 [95% confidence interval 5.279-81.114]).
While PC-RPLND is appropriate in patients with residual masses after chemotherapy, patients with pure choriocarcinoma presenting with significantly elevated hCG levels represent a unique patient population where necrosis is found more often than anticipated.
绒毛膜癌生殖细胞肿瘤较为罕见,通常表现为人绒毛膜促性腺激素(hCG)水平显著升高。在可治愈的情况下,人们普遍认为这主要是化疗的结果。我们旨在确定接受化疗后腹膜后淋巴结清扫术(PC-RPLND)的患者的组织学特征,并将其与具有相似 hCG 水平升高的转移性非精原细胞瘤生殖细胞肿瘤(NSGCT)患者进行比较。
我们回顾了 1988 年至 2017 年间接受 PC-RPLND 的男性患者的病历,这些患者在睾丸切除术后、诱导化疗前的 hCG 水平大于 50,000 mIU/ml。根据原发病灶的组织学进行分层:单纯绒毛膜癌和混合 NSGCT。报告了临床、病理和血清学数据,并使用逻辑回归评估了 PC-RPLND 标本中坏死的预测因素。
我们的队列包括 108 名男性患者。混合组(n=91)的 hCG 中位数为 165,177 mIU/ml,化疗后淋巴结大小为 4.7 cm,其中 19.8%的患者在 RPLND 前还接受了挽救性化疗。单纯绒毛膜癌组(n=17)的 hCG 中位数为 170,267 mIU/ml,淋巴结大小为 5.1 cm,其中 17.6%的患者接受了挽救性化疗。88.2%的绒毛膜癌患者在 PC-RPLND 标本中发现坏死,而混合 NSGCT 组的这一比例为 29.7%(P<0.0001)。控制挽救性化疗的使用、化疗前 hCG、淋巴结大小和标志物状态后,绒毛膜癌患者在 RPLND 标本中发生坏死的可能性是混合 NSGCT 组的 20 倍(优势比 20.68 [95%置信区间 5.279-81.114])。
虽然 PC-RPLND 适用于化疗后残留肿块的患者,但 hCG 水平显著升高的单纯绒毛膜癌患者代表了一个独特的患者群体,其中坏死的发生率高于预期。