University College Hospital NHS Trust, London, UK.
Eur J Cancer. 2012 Jul;48(11):1700-6. doi: 10.1016/j.ejca.2011.10.018. Epub 2011 Nov 15.
To examine whether three cycles of a low-intensity chemotherapy consisting of cyclophosphamide [500 mg/m(2) - day 1], vinblastine [6 mg/m(2) - days 1 and 8] and prednisolone [40 mg/m(2) - days 1-7] (CVP) is safe and therapeutically effective in children and adolescents with early stage nodular lymphocyte predominant Hodgkin lymphoma [nLPHL].
Fifty-five children and adolescents with early stage nLPHL [median age 13 years, range 4-17 years] diagnosed between June 2005 and October 2010 in the UK and France are the subjects of this report. Staging investigations included conventional cross sectional as well as 18 fluro-deoxyglucose [FDG] PET imaging. Histology was confirmed as nLPHL by an expert pathology panel.
Of the 45 patients, who received CVP as first line treatment, 36 [80%, 95% Confidence Interval [CI]: (68; 92)] either achieved a complete remission [CR] or CR unconfirmed [CRu], the remaining nine patients achieved a partial response. All nine subsequently achieved CR with salvage chemotherapy [n=7] or radiotherapy [n=2]. Ten patients received CVP at relapse after primary treatment that consisted of surgery alone and all achieved CR. To date, only three patients have relapsed after CVP chemotherapy and all had received CVP as first line treatment at initial diagnosis. The 40-month freedom from treatment failure and overall survival for the entire cohort were 75.4% (SE ± 6%) and 100%, respectively. No significant early toxicity was observed.
Our results show that CVP is an effective chemotherapy regimen in children and adolescents with early stage nLPHL that is well tolerated with minimal acute toxicity.
研究由环磷酰胺[500mg/m²-第 1 天]、长春碱[6mg/m²-第 1 和 8 天]和泼尼松龙[40mg/m²-第 1-7 天]组成的三个低强度化疗周期(CVP)在儿童和青少年早期结节性淋巴细胞为主型霍奇金淋巴瘤[nLPHL]中的安全性和治疗效果。
本报告的研究对象是 2005 年 6 月至 2010 年 10 月在英国和法国诊断为早期 nLPHL 的 55 例儿童和青少年[中位年龄 13 岁,范围 4-17 岁]。分期检查包括常规横断面成像和 18 氟-脱氧葡萄糖[FDG]PET 成像。组织学由专家病理小组确认为 nLPHL。
45 例接受 CVP 作为一线治疗的患者中,36 例[80%,95%置信区间(68;92)]达到完全缓解[CR]或未确认的完全缓解[CRu],其余 9 例达到部分缓解。所有 9 例随后通过挽救性化疗[n=7]或放疗[n=2]获得 CR。10 例患者在接受单纯手术的初始治疗后复发,接受了 CVP 治疗,均达到 CR。迄今为止,仅 3 例患者在接受 CVP 化疗后复发,且所有患者在初次诊断时均接受 CVP 作为一线治疗。整个队列的 40 个月无治疗失败和总生存率分别为 75.4%(SE±6%)和 100%。未观察到明显的早期毒性。
我们的结果表明,CVP 是儿童和青少年早期 nLPHL 的有效化疗方案,耐受性良好,急性毒性极小。