Abrams J, Doyle L A, Aisner J
University of Maryland Cancer Center, Baltimore 21201.
Semin Oncol. 1988 Jun;15(3):261-77.
New treatment approaches in the fight against SCLC are clearly on the horizon and some are already in clinical trials. With this in mind, several comments concerning future directions in staging this disease can be made: 1. Staging is important and complete staging is needed in order to continue to build meaningful information. 2. Limited/Extensive disease categories are in use and remain important; yet this system is not completely adequate. There are subsets within each group that do better: minimal disease versus bulky disease in limited stage, extraabdominal v intraabdominal in extensive disease, and single organ versus multiple organ involvement. Therefore, a new staging system is needed. The TNM system is designed primarily to define surgical resectability and will thus not adequately address the issues for SCLC unless the N and M categories are markedly enlarged. A staging symposium was recently held in Europe to begin to address potential approaches to staging and an American staging conference is planned. 3. Biomarkers: In the broad range of possible markers, most are not sufficiently sensitive or specific to supplant clinical exam and routine testing. But newer tests such as NSE, CK-BB and tumor surface antigen expression and recognition may impact on staging in the near future. 4. Finally, as the biology of SCLC is further understood, much of the derived understanding will likely change the staging and prognostic factors.
对抗小细胞肺癌(SCLC)的新治疗方法显然即将出现,有些已经在进行临床试验。考虑到这一点,关于该疾病分期未来方向可以提出几点看法:1. 分期很重要,为了持续积累有意义的信息,需要进行完整的分期。2. 目前使用的局限期/广泛期分类仍然很重要;然而,这个系统并不完全足够。每组中都有亚组表现更好:局限期的微小病灶与大块病灶、广泛期的腹外与腹内、单器官受累与多器官受累。因此,需要一个新的分期系统。TNM系统主要用于定义手术可切除性,因此除非显著扩大N和M分类,否则无法充分解决SCLC的问题。欧洲最近召开了一次分期研讨会,开始探讨潜在的分期方法,并且计划召开一次美国分期会议。3. 生物标志物:在众多可能的标志物中,大多数对取代临床检查和常规检测而言不够敏感或特异。但诸如神经元特异性烯醇化酶(NSE)、肌酸激酶BB(CK-BB)以及肿瘤表面抗原表达和识别等更新的检测方法可能在不久的将来影响分期。4. 最后,随着对SCLC生物学特性的进一步了解,由此获得的许多认识可能会改变分期和预后因素。