Wirth Andrew, Yuen Kally, Barton Michael, Roos Daniel, Gogna Kumar, Pratt Gary, Macleod Craig, Bydder Sean, Morgan Graeme, Christie David
Division of Radiation Oncology, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia.
Cancer. 2005 Sep 15;104(6):1221-9. doi: 10.1002/cncr.21303.
The curative potential of radiotherapy (RT) alone as initial treatment for patients with Stage I-II lymphocyte-predominant Hodgkin lymphoma (LPHL) has not been defined well.
Two hundred two patients who were treated between 1969 and 1995 were evaluated in a retrospective, multicenter study.
Patient characteristics were as follows: The median age was 31 years, 75% of patients were male, 80% of patients had Ann Arbor Stage I disease, 1% of patients had bulky disease, 3% of patients had B symptoms, 1% of patients had extranodal involvement, and 80% of patients had supradiaphragmatic disease. The RT fields were a full mantle field in 52% of patients, less than a full mantle field in 24% of patients, an inverted-Y field in 17% of patients, less than an inverted-Y field in 3% of patients, and total lymph node irradiation in 3% of patients. The median dose was 36 Gray. The median follow-up was 15 years. The overall survival (OS) rate at 15 years was 83%, and freedom from progression (FFP) was observed in 82% of patients, including 84% of patients with Stage I disease and 73% of patients with Stage II disease. No recurrent LPHL and only 1 patient with non-Hodgkin lymphoma (NHL) were reported after 15 years. Adverse prognostic factors that were identified on multifactor analysis were as follows: for OS, age 45 years or older (P < 0.0005), the presence of B symptoms (P = 0.002), increasing number of sites (P = 0.015); for FFP, increasing number of sites (P = 0.002). No significant difference was found in FFP in a comparison of patients who received elective mediastinal RT with patients who did not receive mediastinal RT (P = 0.11). Causes of death at 15 years were LPHL in 3% of patients, NHL in 2% of patients, in-field malignancy in 2% of patients, in-field cardiac/respiratory in 4% of patients, and other in 6% of patients.
The current data suggested that RT potentially may be curative for patients with Stage I-II LPHL and raise the possibility that limited-field RT may be used without loss of treatment efficacy. Involved-field RT warrants further investigation for patients with early-stage LPHL.
单独放疗(RT)作为Ⅰ-Ⅱ期淋巴细胞为主型霍奇金淋巴瘤(LPHL)患者的初始治疗的治愈潜力尚未明确界定。
对1969年至1995年间接受治疗的202例患者进行了一项回顾性多中心研究。
患者特征如下:中位年龄为31岁,75%的患者为男性,80%的患者为Ann ArborⅠ期疾病,1%的患者有大包块病变,3%的患者有B症状,1%的患者有结外受累,80%的患者有膈上疾病。放疗野方面,52%的患者为全斗篷野,24%的患者小于全斗篷野,17%的患者为倒Y野,3%的患者小于倒Y野,3%的患者为全淋巴结照射。中位剂量为36格雷。中位随访时间为15年。15年的总生存率(OS)为83%,82%的患者无疾病进展(FFP),包括84%的Ⅰ期疾病患者和73%的Ⅱ期疾病患者。15年后未报告复发性LPHL,仅1例患者发生非霍奇金淋巴瘤(NHL)。多因素分析确定的不良预后因素如下:对于OS,年龄45岁及以上(P<0.0005)、存在B症状(P=0.002)、受累部位数量增加(P=0.015);对于FFP,受累部位数量增加(P=0.002)。接受选择性纵隔放疗的患者与未接受纵隔放疗的患者在FFP方面未发现显著差异(P=0.11)。在15年时,3%的患者死于LPHL,2%的患者死于NHL,2%的患者死于野内恶性肿瘤,4%的患者死于野内心脏/呼吸系统疾病,6%的患者死于其他原因。
目前的数据表明,放疗可能对Ⅰ-Ⅱ期LPHL患者具有治愈作用,并增加了使用局限野放疗而不损失治疗效果的可能性。对于早期LPHL患者,受累野放疗值得进一步研究。