Waterman Tara A, Hagen Jeffrey A, Peters Jeffrey H, DeMeester Steven R, Taylor Clive R, Demeester Tom R
Department of Surgery, Keck School of Medicine, University of Southern California, Los Angeles, California 90033, USA.
Ann Thorac Surg. 2004 Oct;78(4):1161-9; discussion 1161-9. doi: 10.1016/j.athoracsur.2004.04.045.
The number or ratio of lymph node metastases detected by hematoxylin & eosin (H&E) staining is the most important predictor of survival in esophageal cancer. The survival effect of lymph node metastases detected on immunohistochemistry (IHC) is controversial. My colleagues and I hypothesized that the extent of nodal disease determined by both H&E and IHC examination would more accurately predict survival than either technique alone.
The study population consisted of 37 patients who underwent en bloc esophagectomy as primary therapy for esophageal adenocarcinoma 5 or more years ago. All had mediastinal and upper abdominal lymphadenectomy. No patient received neoadjuvant or adjuvant therapy. Tissue blocks were sectioned for H&E staining to confirm the initial histology, and a second slide was stained with monoclonal antibodies AE1 and CAM 5.2, which are directed at a number of cytokeratin antigens. The slides were reviewed by an investigator blinded to clinical outcome. The effect of IHC staining on prognosis was assessed by comparing 5-year survival based on H&E and IHC findings.
A total of 1,970 nodes were examined in the 37 patients. Routine H&E staining detected metastases in 29 patients (78%); the remaining 8 with N0 disease all survived at least 5 years after operation (median not reached). In the 29 patients with N1 disease, survival was 41% at 5 years. In 20 of the 29 N1 patients, metastases were detected by H&E in less than 10% of the nodes removed; 55% of the patients survived 5 years, and 39% survived 8 years. Nine of the 29 patients had metastases detected in more than 10% of the nodes removed, and all died at a median of 17 months. IHC staining was performed on the nodes from the 8 N0 patients and the 20 patients with less than 10% nodal involvement (a total of 28 patients). Additional nodal metastases, not identified on H&E examination, were found in 51 nodes from 17 patients (60.7%). Of the 8 patients who were node negative on H&E examination, 3 had metastases detected by IHC, and all survived 5 years or more free of disease. Of the 20 patients with less than 10% nodal metastases on H&E, 14 (70%) had additional metastases detected by IHC (median, 2 nodes per patient). When combined with the results of H&E staining, the node ratio remained less than 10% in 13 patients and exceeded 10% in 7. Survival in patients whose ratio remained less than 10% was significantly better than in those whose ratio exceeded 10% (actual 5-year survival, 77% vs 14%; chi2 = 4.662; p = 0.03).
IHC staining techniques can identify nodal metastases missed by routine H&E examination in a large number of patients. The combination of H&E and IHC examination is useful in patients with less than 10% nodal involvement by H&E examination in that IHC detection of micrometastases allows classification into low-risk (> 75% survival) and high-risk (< 15% survival) groups. IHC-detected micrometastases are not of prognostic importance in N0 patients or those with greater than 10% nodal metastases on H&E.
苏木精-伊红(H&E)染色检测到的淋巴结转移数量或比例是食管癌生存的最重要预测指标。免疫组织化学(IHC)检测到的淋巴结转移对生存的影响存在争议。我和同事们推测,通过H&E和IHC检查共同确定的淋巴结病变范围比单独使用任何一种技术能更准确地预测生存情况。
研究人群包括37例5年或更久之前接受食管癌整块切除术作为主要治疗的患者。所有患者均接受了纵隔和上腹部淋巴结清扫术。没有患者接受新辅助或辅助治疗。将组织块切片进行H&E染色以确认初始组织学,另一张玻片用针对多种细胞角蛋白抗原的单克隆抗体AE1和CAM 5.2染色。玻片由对临床结果不知情的研究人员进行评估。通过比较基于H&E和IHC结果的5年生存率来评估IHC染色对预后的影响。
37例患者共检查了1970个淋巴结。常规H&E染色在29例患者(78%)中检测到转移;其余8例N0疾病患者术后均存活至少5年(未达到中位数)。在29例N1疾病患者中,5年生存率为41%。在29例N1患者中的20例中,H&E在切除的淋巴结中检测到转移的比例不到10%;55%的患者存活5年,39%的患者存活8年。29例患者中的9例在切除的淋巴结中检测到转移的比例超过10%,所有患者均在中位时间17个月时死亡。对8例N0患者和20例淋巴结受累比例小于10%的患者(共28例)的淋巴结进行IHC染色。在17例患者(60.7%)的51个淋巴结中发现了H&E检查未发现的额外淋巴结转移。在H&E检查淋巴结阴性的8例患者中,3例通过IHC检测到转移,且均存活5年或更长时间且无疾病。在H&E检查淋巴结转移比例小于10%的20例患者中,14例(70%)通过IHC检测到额外转移(中位数为每位患者2个淋巴结)。当与H&E染色结果相结合时,13例患者的淋巴结比例仍小于10%,7例患者的淋巴结比例超过10%。淋巴结比例仍小于10%的患者的生存率明显高于比例超过10%的患者(实际5年生存率,77%对14%;χ2 = 4.662;p = 0.03)。
IHC染色技术可以在大量患者中识别常规H&E检查遗漏的淋巴结转移。对于H&E检查淋巴结受累比例小于10%的患者,H&E和IHC检查相结合是有用的,因为通过IHC检测微转移可以将患者分为低风险(生存率>75%)和高风险(生存率<15%)组。在N0患者或H&E检查淋巴结转移比例大于10%的患者中,IHC检测到的微转移对预后无重要意义。