Kushner B H, Cheung N K, LaQuaglia M P, Ambros P F, Ambros I M, Bonilla M A, Ladanyi M, Gerald W L
Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
J Clin Oncol. 1996 Jul;14(7):2174-80. doi: 10.1200/JCO.1996.14.7.2174.
To gain insight into the management of non-metastatic neuroblastoma by examining clinical and biologic features of International Neuroblastoma Staging System (INSS) stage 1 tumors.
Patients were staged by both the INSS and the Evans staging system and were evaluated for biologic prognostic factors. Patients with INSS stage 1 received no cytotoxic therapy. The literature was reviewed for clinical and biologic data about INSS stage 1.
We evaluated 10 consecutive patients (median age, 17.5 months) with INSS stage 1; all remain disease-free (median follow-up duration, > 5 years). Tumors were in the abdomen (n = 6), chest (n = 3), or pelvis (n = 1). Neuroblastoma involved margins of resection in six tumors. Poor-prognostic biologic findings included tumor-cell diploidy (n = 2) and unfavorable Shimada histopathology (n = 2). Two patients were to receive chemotherapy for, respectively, a tumor deemed unresectable and a tumor classified as Evans stage III; second opinions resulted in surgical management alone in each case. Published reports confirm that some INSS stage 1 patients (1) are at risk for overtreatment, and (2) have poor-prognostic biologic findings yet do well.
Surgery alone suffices for INSS stage 1 neuroblastoma, even if biologic prognostic factors are unfavorable, microscopic disease remains after surgery, and tumor size is suggestive of "advanced-stage" status in other staging systems. Attempts to resect regionally confined neuroblastomas should take precedence over immediate use of cytotoxic therapy; otherwise, some patients may receive chemotherapy or radiotherapy unnecessarily.
通过研究国际神经母细胞瘤分期系统(INSS)1期肿瘤的临床和生物学特征,深入了解非转移性神经母细胞瘤的治疗方法。
采用INSS和埃文斯分期系统对患者进行分期,并评估生物学预后因素。INSS 1期患者未接受细胞毒性治疗。回顾了关于INSS 1期的临床和生物学数据的文献。
我们评估了10例连续的INSS 1期患者(中位年龄17.5个月);所有患者均无疾病复发(中位随访时间>5年)。肿瘤位于腹部(n = 6)、胸部(n = 3)或骨盆(n = 1)。6例肿瘤的神经母细胞瘤累及手术切缘。预后不良的生物学表现包括肿瘤细胞二倍体(n = 2)和不良的岛田组织病理学(n = 2)。两名患者分别因肿瘤被认为无法切除和肿瘤被分类为埃文斯III期而接受化疗;经再次会诊,每例均仅采用手术治疗。已发表的报告证实,一些INSS 1期患者(1)有过度治疗的风险,(2)生物学预后表现不佳,但预后良好。
对于INSS 1期神经母细胞瘤,即使生物学预后因素不利、手术后仍有微小病灶残留且肿瘤大小在其他分期系统中提示“晚期”状态,单纯手术治疗也足够。尝试切除局限性神经母细胞瘤应优先于立即使用细胞毒性治疗;否则,一些患者可能会不必要地接受化疗或放疗。