Pitz Cordula C M, de la Rivière Aart Brutel, van Swieten Henry A, Duurkens Vincent A M, Lammers Jan-Willem J, van den Bosch Jules M M
Department of Pulmonology, Sint Antonius Hospital, 3430 EM Nieuwegein, The Netherlands.
Eur J Cardiothorac Surg. 2004 Jul;26(1):202-8. doi: 10.1016/j.ejcts.2004.02.016.
Due to its localisation in the apex of the lung with invasion of the lower part of the brachial plexus, first ribs, vertebrae, subclavian vessels or stellate ganglion, a superior sulcus tumour causes characteristic symptoms, like arm or shoulder pain or Horner's syndrome. If rib invasion is the only feature, lysis of the rib must be evident on the chest radiograph; otherwise the tumour cannot be defined as a Pancoast tumour. It is important to adequately stage the tumour, because staging significantly influences survival. Survival is better for T3 than T4 tumours and mediastinal lymph node involvement has been found to be a negative prognostic factor. Also Horner's syndrome and incompleteness of resection worsen survival. The management of superior sulcus tumours has evolved over the past 50 years. Before 1950 it was considered to be inoperable and uniformly fatal. Shaw and Paulson introduced combined modality treatment and for many years, this combination of radiotherapy and surgery was the treatment of choice with a mean 5-year survival of approximately 30%. Postoperative radiotherapy or brachytherapy does not improve survival in patients with complete or incomplete resection. The tumour can be resected through the classic posterior Shaw-Paulson approach or the newer anterior transcervical approach, introduced by Dartevelle. This method facilitates better exposure of the extreme apex of the lung, brachial plexus and subclavian vessels. Regarding the extent of pulmonary resection, en bloc resection of the involved ribs with a lobectomy is recommended. Recent multimodality studies, involving chemoradiotherapy and surgical resection, show promising results regarding completeness of resection, local recurrence and survival, provided that appropriate staging has been carried out. However, careful patient selection and adequate perioperative management with protection of the bronchial stump or anastomosis are important to achieve reasonable rates of morbidity and mortality. As brain metastases remain one of the most common forms of relapse, further studies are needed to examine the role of prophylactic cranial irradiation in patients with complete resection. Also the addition of other chemotherapy agents or biologic agents such as angiogenesis inhibitors or tyrosine kinase inhibitors gives a new perspective in the treatment of Pancoast tumours.
由于肺尖部肿瘤侵犯臂丛神经下部、第一肋骨、椎体、锁骨下血管或星状神经节,肺上沟瘤会引发特征性症状,如手臂或肩部疼痛或霍纳综合征。如果仅存在肋骨侵犯这一特征,胸部X线片上必须显示肋骨溶解;否则该肿瘤不能被定义为潘科斯特瘤。对肿瘤进行充分分期很重要,因为分期会显著影响生存率。T3期肿瘤的生存率高于T4期肿瘤,且已发现纵隔淋巴结受累是一个负面预后因素。此外,霍纳综合征和切除不完全会使生存率降低。在过去50年中,肺上沟瘤的治疗方法不断演变。1950年以前,人们认为它无法手术切除且必死无疑。肖和保尔森引入了综合治疗模式,多年来,放疗和手术相结合一直是首选治疗方法,平均5年生存率约为30%。术后放疗或近距离放疗并不能提高完全或不完全切除患者的生存率。该肿瘤可通过经典的后外侧肖-保尔森入路或达特韦尔引入的较新的前经颈入路进行切除。这种方法便于更好地暴露肺尖、臂丛神经和锁骨下血管。关于肺切除范围,建议将受累肋骨与肺叶整块切除。近期涉及放化疗和手术切除的多模式研究在切除完整性、局部复发和生存率方面显示出了有前景的结果,前提是已进行了适当的分期。然而,仔细的患者选择和充分的围手术期管理以及对支气管残端或吻合口的保护对于实现合理的发病率和死亡率至关重要。由于脑转移仍然是最常见的复发形式之一,需要进一步研究以探讨预防性颅脑照射在完全切除患者中的作用。此外,添加其他化疗药物或生物制剂,如血管生成抑制剂或酪氨酸激酶抑制剂,为潘科斯特瘤的治疗提供了新的视角。