Sheth D S, Yasko A W, Raymond A K, Ayala A G, Carrasco C H, Benjamin R S, Jaffe N, Murray J A
Department of Surgical Oncology, University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.
Cancer. 1996 Nov 15;78(10):2136-45.
Dedifferentiated parosteal osteosarcoma (dd-POS) designates high grade transformation, of conventional low grade parosteal osteosarcoma (c-POS). The paradigm of preoperative diagnosis, neoadjuvant chemotherapy, and wide local excision has not been adequately evaluated for dd-POS, as it has been for conventional high grade intramedullary osteosarcoma.
A retrospective review was conducted of 28 patients treated at the authors' institution between January 1980 and December 1992 for an osteosarcoma arising on the surface of the bone diagnosed as either c-POS or dd-POS. The clinicopathologic features, diagnosis, treatment, and patient outcome were analyzed.
A dedifferentiated component was identified in 12 of 28 tumors (43%). Neither the presence of radiolucencies (77% in c-POS and 100% in dd-POS, P = 0.06) nor medullary invasion (42% in c-POS and 50% in dd-POS, P = 0.28) distinguished dd-POS from c-POS. However, all patients who presented with focal hypervascularity on an arteriogram defined the high grade component of dd-POS that was confirmed by selective needle biopsy. This differed significantly (P = 0.00003) from c-POS. None of the patients with c-POS died of the disease (median survival duration, 77 months; range, 16-152 months). Six patients (35%) developed a local recurrence, but five were treated successfully with further surgery. In the dd-POS group, 7 of the 12 patients died of the disease. Ten patients with dd-POS received preoperative chemotherapy (IA cis-diamminedichloroplatinum, IV doxorubicin), and a good response (> 90% necrosis of high grade component) was observed in four. Among patients whose disease was localized, continuous disease free survival was prolonged significantly (P = 0.03) in patients with a good response (median, 75 months) compared with those who responded poorly (median, 13 months). Five patients remained continuously disease free (median, 66 months, range, 29-95 months).
Wide surgical excision alone is adequate treatment for patients with c-POS. Recognition of dedifferentiated areas with angiography and percutaneous biopsy of hypervascular areas should prompt the administration of chemotherapy and wide local excision to optimize patient outcome.
去分化骨旁骨肉瘤(dd-POS)指传统的低级别骨旁骨肉瘤(c-POS)发生高级别转化。术前诊断、新辅助化疗及广泛局部切除的模式在dd-POS中尚未得到充分评估,而在传统的高级别髓内骨肉瘤中已得到充分评估。
对1980年1月至1992年12月在作者所在机构接受治疗的28例起源于骨表面的骨肉瘤患者进行回顾性研究,这些骨肉瘤被诊断为c-POS或dd-POS。分析其临床病理特征、诊断、治疗及患者预后。
28例肿瘤中有12例(43%)发现有去分化成分。透亮区的存在(c-POS中为77%,dd-POS中为100%,P = 0.06)及髓腔侵犯(c-POS中为42%,dd-POS中为50%,P = 0.28)均不能区分dd-POS与c-POS。然而,所有动脉造影显示有局灶性血管增多的患者均确定为dd-POS的高级别成分,经选择性针吸活检得以证实。这与c-POS有显著差异(P = 0.00003)。c-POS患者均未死于该病(中位生存时间77个月;范围16 - 152个月)。6例患者(35%)出现局部复发,但5例经进一步手术成功治疗。在dd-POS组,12例患者中有7例死于该病。10例dd-POS患者接受了术前化疗(动脉内顺铂、静脉内阿霉素),4例观察到良好反应(高级别成分坏死> 90%)。在疾病局限的患者中,反应良好的患者(中位时间75个月)与反应较差的患者(中位时间13个月)相比,无病生存期显著延长(P = 0.03)。5例患者持续无病生存(中位时间66个月,范围29 - 95个月)。
对于c-POS患者,单纯广泛手术切除即为充分的治疗。通过血管造影识别去分化区域并对血管增多区域进行经皮活检,应促使给予化疗及广泛局部切除以优化患者预后。