Rosenblatt E, Kuten A, Leviov M, Cederbaum M
Radiotherapy Unit, Department of Oncology, Rambam Medical Center and Technion-Israel Institute of Technology, Haifa.
Leuk Lymphoma. 1998 Jun;30(1-2):143-51. doi: 10.3109/10428199809050937.
This study was undertaken to analyze the influence of total skin dose and dose-fractionation schedules on the response rate, survival and skin toxicity of patients with mycosis fungoides [MF] treated with total skin electron irradiation [TSEI]. From 1979 to 1992, 40 patients with MF were treated with TSEI using a modified Christie Hospital technique. Mean follow-up time was 48 months [median 20 months]. 37/40 patients completed TSEI; three died due to non-treatment-related conditions during therapy. 34/37 [92%] treated patients achieved complete remission [CR] and 16/40 [40%] are alive with no evidence of disease. Over the years, changes in dose-fractionation schedules were made and correlated with the pattern of CR and skin toxicity. The 5-year actuarial survival [Stanford staging] was 84% in Stages IA-IB [all Stage IA patients are alive] and 59% in Stage II. The probability of survival of Stage III-IV patients was 30% at 30 months. Late skin toxicity was mild to moderate in 60% and severe in 25% of patients. A reduction of the total dose and dose-per-fraction resulted in an acceptable CR rate and a significantly lower toxicity. TSEI is effective in early stage MF. Skin control and late skin toxicity seem to be dose-fractionation-schedule related. For the early stages, the optimal treatment schedule seems to be 24-30 Gy to the whole skin surface in 2.4-3.0 Gy fractions, given twice weekly over a period of four to six weeks. Total doses of 24-30 Gy at 2.4-3.0 Gy per fraction yielded comparable skin control rates with lower skin toxicity.
本研究旨在分析全身皮肤剂量和剂量分割方案对蕈样肉芽肿(MF)患者接受全身皮肤电子照射(TSEI)治疗时的缓解率、生存率和皮肤毒性的影响。1979年至1992年,40例MF患者采用改良的克里斯蒂医院技术接受TSEI治疗。平均随访时间为48个月(中位数20个月)。40例患者中有37例完成了TSEI治疗;3例在治疗期间因非治疗相关疾病死亡。37例接受治疗的患者中有34例(92%)达到完全缓解(CR),40例中有16例(40%)无疾病证据存活。多年来,剂量分割方案发生了变化,并与CR模式和皮肤毒性相关。IA - IB期的5年精算生存率(斯坦福分期)为84%(所有IA期患者均存活),II期为59%。III - IV期患者在30个月时的生存概率为30%。60%的患者晚期皮肤毒性为轻度至中度,25%为重度。总剂量和每次分割剂量的降低导致了可接受的CR率和显著更低的毒性。TSEI对早期MF有效。皮肤控制和晚期皮肤毒性似乎与剂量分割方案有关。对于早期阶段,最佳治疗方案似乎是对整个皮肤表面给予24 - 30 Gy,分2.4 - 3.0 Gy的分割剂量,每周两次,持续四至六周。每次分割剂量为2.4 - 3.0 Gy、总剂量为24 - 30 Gy时,可产生相当的皮肤控制率且皮肤毒性更低。