Lee J D, Ginsberg R J
Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Ann Thorac Surg. 1996 Aug;62(2):338-41.
The accurate preoperative staging of lung cancer remains an essential element in its proper treatment. In most centers, N3 disease contraindicates an operative approach, despite the advent of combined modality therapy. Although it is used to confirm palpable supraclavicular disease, routine scalene lymph node biopsy to stage nonpalpable disease has been abandoned.
From January 1991 to July 1995, 408 cervical mediastinoscopies were performed by a single surgeon for the staging of lung cancer. In those patients eligible for induction therapy, when N2 or N3 disease was strongly suspected or identified, ipsilateral scalene lymph node biopsy was performed through the same cervical incision using the mediastinoscope to reach the scalene fat pad.
Eighty-one patients underwent this additional staging procedure. There was minimal morbidity and no deaths. Of these 81 fully staged patients, primary tumor histology was non-small cell in 95.1%. Thirty-nine patients were staged as N2 after standard mediastinoscopy. Of these, 6 (15.4%) harbored occult nonpalpable supraclavicular lymph node disease as well. Nineteen patients were staged as N3-contralateral after standard mediastinoscopy. Of these, 13 (68.4%) had occult supraclavicular disease as well. Of all 58 patients with superior mediastinal nodal involvement identified by standard mediastinoscopy, 19 (32.8%) also harbored occult scalene lymph node disease, rendering them ineligible for our induction therapy protocols. Scalene positive primary tumors were all centrally located (visualizable by flexible bronchoscopy) (19 of 19) and were uniformly of nonsquamous origin.
We believe that this technique is a valuable extension to standard cervical mediastinoscopy and can be used in N2 or N3 staged patients with central, nonsquamous tumors before considering a combined modality therapeutic approach that includes operation. Through its use, more accurate staging before initiation of therapy and elimination of those patients who may derive no benefit from an aggressive surgical approach may be possible.
肺癌准确的术前分期仍是其恰当治疗的关键要素。在大多数中心,尽管联合治疗方式已出现,但N3期疾病仍不适合手术治疗。虽然常规斜角肌淋巴结活检用于确诊可触及的锁骨上疾病,但已不再用于对不可触及疾病进行分期。
1991年1月至1995年7月,由一名外科医生进行了408例用于肺癌分期的颈部纵隔镜检查。对于那些适合诱导治疗的患者,当强烈怀疑或确定为N2或N3期疾病时,通过相同的颈部切口,使用纵隔镜到达斜角肌脂肪垫进行同侧斜角肌淋巴结活检。
81例患者接受了这一额外的分期程序。发病率极低,无死亡病例。在这81例完成分期的患者中,95.1%的原发性肿瘤组织学类型为非小细胞癌。39例患者在标准纵隔镜检查后被分期为N2期。其中,6例(15.4%)还存在隐匿性不可触及的锁骨上淋巴结疾病。19例患者在标准纵隔镜检查后被分期为N3期(对侧)。其中,13例(68.4%)也存在隐匿性锁骨上疾病。在通过标准纵隔镜检查确定的所有58例上纵隔淋巴结受累患者中,19例(32.8%)也存在隐匿性斜角肌淋巴结疾病,使其不符合我们的诱导治疗方案。斜角肌阳性的原发性肿瘤均位于中央(可通过可弯曲支气管镜观察到)(19例中的19例),且均为非鳞状起源。
我们认为,这项技术是对标准颈部纵隔镜检查的有价值扩展,可用于N2或N3期、中央型、非鳞状肿瘤患者,在考虑包括手术在内的联合治疗方法之前。通过使用该技术,可能在治疗开始前进行更准确的分期,并排除那些可能无法从积极手术方法中获益的患者。