Steyerberg E W, Keizer H J, Messemer J E, Toner G C, Schraffordt Koops H, Fosså S D, Gerl A, Sleijfer D T, Donohue J P, Habbema J D
Department of Public Health, Erasmus University, Rotterdam, The Netherlands.
Cancer. 1997 Jan 15;79(2):345-55.
After chemotherapy for a metastatic nonseminomatous germ cell tumor, pulmonary masses may be seen on a computed tomography scan. These residual masses may contain one of three histologic elements: necrosis, mature teratoma, or cancer. Because surgical resection of masses containing only necrosis is unnecessary, the authors aimed to predict the histology of these residual masses.
Six study groups contributed patient data on a total of 215 patients undergoing thoracotomy after cisplatin-based induction chemotherapy for metastatic testicular nonseminomatous germ cell tumors. Logistic regression analysis was used to estimate the probability of necrosis, mature teratoma, and cancer in relation to predictors known before thoracotomy.
The pulmonary mass histology was necrosis in 116 patients (54%), mature teratoma in 70 (33%), and cancer in 29 (13%). Necrosis was found at thoracotomy in 89% of those patients with necrosis at retroperitoneal lymph node dissection (RPLND). Other predictors included the primary tumor histology, prechemotherapy tumor marker levels, change in mass size during chemotherapy, and the presence of a single, unilateral mass. Multivariate combination of predictors yielded reliable models (goodness-of-fit tests, P > 0.20), which discriminated necrosis well from other histologies, especially if RPLND histology was available (area under the receiver operating characteristic curve, 0.86).
This analysis indicated subgroups of patients with a high probability of necrosis and a low risk of cancer for whom close follow-up of the residual pulmonary mass might be considered. In most patients, a RPLND should be performed before a thoracotomy is considered, because the probability of necrosis is generally higher at thoracotomy than at RPLND and the histology at RPLND is a strong predictor of the histology at thoracotomy.
转移性非精原细胞性生殖细胞肿瘤化疗后,计算机断层扫描可能会发现肺部肿块。这些残留肿块可能包含三种组织学成分之一:坏死、成熟畸胎瘤或癌。由于仅包含坏死的肿块无需手术切除,作者旨在预测这些残留肿块的组织学类型。
六个研究组提供了215例接受顺铂为主的诱导化疗后行开胸手术的转移性睾丸非精原细胞性生殖细胞肿瘤患者的数据。采用逻辑回归分析来估计与开胸手术前已知预测因素相关的坏死、成熟畸胎瘤和癌的概率。
肺部肿块组织学类型为坏死的有116例患者(54%),成熟畸胎瘤70例(33%),癌29例(13%)。在腹膜后淋巴结清扫术(RPLND)时发现坏死的患者中,89%在开胸手术时也发现坏死。其他预测因素包括原发肿瘤组织学类型、化疗前肿瘤标志物水平、化疗期间肿块大小变化以及单个单侧肿块的存在。预测因素的多变量组合产生了可靠的模型(拟合优度检验,P > 0.20),能很好地区分坏死与其他组织学类型,尤其是在有RPLND组织学结果时(受试者操作特征曲线下面积为0.86)。
该分析表明,对于坏死可能性高且癌症风险低的患者亚组,可考虑对残留肺部肿块进行密切随访。在大多数患者中,应在考虑开胸手术前进行RPLND,因为开胸手术时坏死的概率通常高于RPLND,且RPLND的组织学类型是开胸手术组织学类型的有力预测指标。