Waddell A E, Davis A M, Ahn H, Wunder J S, Blackstein M E, Bell R S
University Musculoskeletal Oncology Unit, Mount Sinai Hospital, Ont.
Can J Surg. 1999 Jun;42(3):190-9.
To evaluate the role of chemotherapy with a combination of doxorubicin (adriamycin) and cisplatin in high-grade, nonosteogenic, non-Ewing's sarcoma (non-OSA) of bone.
A case series comparison with a literature-derived control group.
A university-affiliated tertiary care centre.
Thirty patients with a diagnosis of non-OSA. Of these, 8 had low-grade disease (grade 1 or 2) and 22 had high-grade disease (grade 3). Eleven of the 22 with high-grade disease had malignant fibrous histiocytoma. Seventeen patients with nonmetastatic high-grade non-OSA were compared with a literature cohort of 37 patients who met the eligibility criteria of nonmetastatic, high-grade non-OSA treated with surgery, with or without radiotherapy. The mean follow-up was 25.2 months.
Eight patients with low-grade tumour underwent surgery alone; 22 patients with high-grade tumour underwent surgery and 6 courses of adriamycin (75 mg/m2 every 3 weeks) and cisplatin (100 mg/m2 every 3 weeks).
Disease-free survival and overall survival in those with high-grade tumours treated with or without chemotherapy.
Of 8 patients who had low-grade tumours and underwent surgery alone, 3 had systemic relapse. Of the 22 having high-grade tumours, 4 did not receive chemotherapy because of age and comorbid conditions. Of the other 18, 13 received 3 courses of chemotherapy preoperatively and 3 courses postoperatively, 4 received all 6 courses postoperatively and 1 received all chemotherapy preoperatively to treat metastatic disease. In the 17-patient cohort used for comparison with the literature control group, disease-free survival was 57% at a mean follow-up of 25.6 months and overall survival was 57% at a mean follow-up of 30.1 months. In the control group, disease-free survival was 16% at a mean follow-up of 20.9 months and overall survival was 26% at a mean follow-up of 29.9 months. These differences are significant: p = 0.0000, chi 2 = 41.61 for disease-free survival and p = 0.0000, chi 2 = 46.49 for overall survival.
The findings of this study support the use of adjuvant chemotherapy in patients with high-grade non-OSA, in whom malignant fibrous histiocytoma was the predominant histologic subtype.
评估阿霉素(多柔比星)和顺铂联合化疗在高级别、非骨肉瘤性、非尤文肉瘤(非骨肉瘤性骨肿瘤,non-OSA)中的作用。
与文献对照组进行病例系列比较。
一所大学附属的三级医疗中心。
30例诊断为非骨肉瘤性骨肿瘤的患者。其中,8例为低级别疾病(1级或2级),22例为高级别疾病(3级)。22例高级别疾病患者中有11例为恶性纤维组织细胞瘤。将17例非转移性高级别非骨肉瘤性骨肿瘤患者与37例符合非转移性、高级别非骨肉瘤性骨肿瘤手术治疗(伴或不伴放疗)入选标准的文献队列进行比较。平均随访时间为25.2个月。
8例低级别肿瘤患者仅接受手术治疗;22例高级别肿瘤患者接受手术治疗,并接受6个疗程的阿霉素(每3周75mg/m²)和顺铂(每3周100mg/m²)化疗。
接受或未接受化疗的高级别肿瘤患者的无病生存期和总生存期。
8例低级别肿瘤且仅接受手术治疗的患者中,3例出现全身复发。22例高级别肿瘤患者中,4例因年龄和合并症未接受化疗。在其他18例患者中,13例术前接受3个疗程化疗,术后接受3个疗程化疗,4例术后接受全部6个疗程化疗,1例术前接受全部化疗以治疗转移性疾病。在用于与文献对照组比较的17例患者队列中,平均随访25.6个月时无病生存率为57%,平均随访30.1个月时总生存率为57%。在对照组中,平均随访20.9个月时无病生存率为16%,平均随访29.9个月时总生存率为26%。这些差异具有统计学意义:无病生存期p = 0.0000,χ² = 41.61;总生存期p = 0.0000,χ² = 46.49。
本研究结果支持对高级别非骨肉瘤性骨肿瘤患者使用辅助化疗,其中恶性纤维组织细胞瘤是主要的组织学亚型。