Donaldson Sarah S, Hudson Melissa M, Lamborn Kathleen R, Link Michael P, Kun Larry, Billett Amy Louise, Marcus Karen C, Hurwitz Craig A, Young Jeffrey A, Tarbell Nancy J, Weinstein Howard J
Stanford University Medical Center, Stanford, CA, USA.
J Clin Oncol. 2002 Jul 15;20(14):3081-7. doi: 10.1200/JCO.2002.12.101.
To evaluate outcome and assess toxicity of children and adolescents with early-stage, favorable Hodgkin's disease treated with vinblastine, doxorubicin, methotrexate, and prednisone (VAMP) and low-dose, involved-field radiation.
One hundred ten patients with clinical stages I and II, favorable (nonbulky) Hodgkin's disease were treated with four cycles of VAMP chemotherapy and 15 Gy involved-field radiation for those who achieved a complete response, or 25.5 Gy for those who achieved a partial response to two cycles of VAMP.
With a median follow-up of 5.6 years (range, 1.1 to 10.4 years), the 5-year survival and event-free survival were 99% (lower confidence limit [CL], 97.4%) and 93% (lower CL, 88.6%), respectively. Factors associated with event-free survival of 100% were complete response to two cycles of VAMP and histology other than nodular sclerosing Hodgkin's disease (NSHD). No serious early or late toxicity has been observed. Patients presenting with clinical stages I and IIA, nonbulky disease involving fewer than three nodal sites have a projected survival and event-free survival of 100% and 97% (lower CL, 93%), respectively, at 5 years.
Risk-adapted, combined-modality therapy using only four cycles of VAMP chemotherapy with 15 to 25.5 Gy of involved-field radiation for patients with early-stage/favorable Hodgkin's disease is highly effective and without demonstrable late effects. These results indicate that pediatric patients with stages I and II favorable Hodgkin's disease can be cured with limited therapy that does not include an alkylating agent, bleomycin, etoposide, or high-dose, extended-field radiation therapy.
评估长春花碱、阿霉素、甲氨蝶呤和泼尼松(VAMP)联合低剂量累及野放疗治疗儿童和青少年早期预后良好型霍奇金病的疗效及毒性。
110例临床Ⅰ期和Ⅱ期、预后良好(无大包块)的霍奇金病患者接受4个周期的VAMP化疗,对达到完全缓解的患者给予15 Gy累及野放疗,对VAMP化疗2个周期后达到部分缓解的患者给予25.5 Gy累及野放疗。
中位随访5.6年(范围1.1至10.4年),5年生存率和无事件生存率分别为99%(置信下限[CL],97.4%)和93%(置信下限,88.6%)。与100%无事件生存率相关的因素是对VAMP化疗2个周期的完全缓解以及除结节硬化型霍奇金病(NSHD)以外的组织学类型。未观察到严重的早期或晚期毒性。临床Ⅰ期和ⅡA期、累及少于3个淋巴结部位的无大包块疾病患者,预计5年生存率和无事件生存率分别为100%和97%(置信下限,93%)。
对于早期/预后良好型霍奇金病患者,采用仅4个周期的VAMP化疗联合15至25.5 Gy累及野放疗的风险适应性联合治疗方案高效且无明显晚期效应。这些结果表明,Ⅰ期和Ⅱ期预后良好型霍奇金病的儿科患者可通过不包括烷化剂、博来霉素、依托泊苷或高剂量扩大野放疗的有限治疗治愈。