Raida L, Papajík T, Indrák K, Herman M, Paucek B, Zapletalová J
Hemato-onkologická klinika Lékarské fakulty UP a FN Olomouc.
Vnitr Lek. 2007 Jan;53(1):31-7.
Chemotherapy of BOVAPEC is the modification of temporary intensified Stanford V protocol, an effective primary treatment of advanced Hodgkin's lymphoma (HL) in spite of limited toxicity. Nitrogen mustard was substituted by less myelotoxic cyclophosphamide and the protocol has been used in the treatment of patients with an intermediate stage of HL.
The primary treatment with BOVAPEC was started in 62 patients. Complete chemotherapy schedule was administered to 60 patients (97%) and the median of its overall duration was 13 (12-18) weeks. 31 patients (50 %) underwent adjuvant "involved field" radiotherapy (RT). The median of posttherapeutic follow-up was 37 (range 8-85) months.
During the treatment, a neutropenia of grade 3 and 4 was observed in 14 patients (23%) but without the development of any serious infectious complications. The manifestation of early non-hematological toxicity did not overcome grade 2.58 patients (94%) achieved the complete remission of HL. A relapse was observed in 11 cases (19%) and estimated five years disease-free survival (DFS) is 72%. The combination of BOVAPEC and RT in primary treatment was associated with higher probability of five years DFS but actually without statistical significance (88% vs. 58%; p = 0.08).
The BOVAPEC regimen with its acceptable toxicity may represent effective primary therapeutic approach to the patients with the intermediate stage of HL. Adjuvant RT is essential in all patients diagnosed with nodal bulk and/or residual lymphadenomegaly.
BOVAPEC化疗方案是对临时强化的斯坦福V方案的改良,尽管毒性有限,但它是晚期霍奇金淋巴瘤(HL)的一种有效初始治疗方法。用骨髓毒性较小的环磷酰胺替代了氮芥,该方案已用于治疗HL中期患者。
62例患者开始采用BOVAPEC进行初始治疗。60例患者(97%)完成了完整的化疗疗程,其总疗程的中位数为13(12 - 18)周。31例患者(50%)接受了辅助性“受累野”放疗(RT)。治疗后随访的中位数为37(范围8 - 85)个月。
治疗期间,14例患者(23%)出现3级和4级中性粒细胞减少,但未发生任何严重感染并发症。早期非血液学毒性表现未超过2级。58例患者(94%)实现了HL的完全缓解。11例(19%)出现复发,估计五年无病生存率(DFS)为72%。BOVAPEC与RT联合用于初始治疗时,五年DFS概率较高,但实际上无统计学意义(88%对58%;p = 0.08)。
BOVAPEC方案毒性可接受,可能是HL中期患者有效的初始治疗方法。对于所有诊断为有淋巴结肿大和/或残留淋巴结肿大的患者,辅助性放疗至关重要。