Tsang R W, Gospodarowicz M K, Sutcliffe S B, Sturgeon J F, Panzarella T, Patterson B J
Department of Radiation Oncology, Princess Margaret Hospital, Toronto, Ontario, Canada.
Int J Radiat Oncol Biol Phys. 1993 Oct 20;27(3):599-604. doi: 10.1016/0360-3016(93)90385-9.
Non-Hodgkin's lymphoma presenting in the thyroid gland is uncommon. A review of the Princess Margaret Hospital experience was performed to assess treatment outcome and prognostic factors in this rare extranodal presentation of localized lymphoma.
Fifty-two patients treated at the PMH between 1978 and 1986 were identified and their records reviewed retrospectively. Staging procedures revealed 16 patients with Stage I, 28 with Stage II, and eight with Stages III or IV disease. Five patients were treated on a protocol designed for anaplastic carcinoma of thyroid and they were excluded from detailed analysis. Of 39 patients with Stages I and II disease, 18 were treated with radiotherapy alone, three chemotherapy alone, and 18 combined modality therapy. Combined modality therapy was used mainly in patients with large tumor bulk.
The overall 5-year actuarial survival and cause-specific survival were 56% and 64%, respectively. The overall relapse-free rate was 61% at 5 years. Among the 39 patients with Stages I and II disease, the 5-year actuarial survival, cause-specific survival, and relapse-free rate were 64%, 73%, and 66%, respectively. There were no significant differences in outcome between those treated with radiotherapy alone and those treated with combined modality therapy (cause-specific survival: p = 0.25, relapse: p = 0.06). A univariate analysis showed that the only variable to reach statistical significance was tumor bulk. Age was marginally significant while stage and histology were not statistically significant, possibly due to the fairly homogeneous distribution of patients in each of these variables. Patients with progression or relapse of lymphoma after initial treatment frequently died of disease. Isolated gastrointestinal relapses occurred in three cases, representing 27% of all relapses.
Based on the above results, we recognize that the majority of patients with localized thyroid lymphoma require combined modality therapy and we recommend radiotherapy alone only for a small, select group of patients with Stage I disease and small tumor bulk.
甲状腺非霍奇金淋巴瘤并不常见。对玛格丽特公主医院的病例进行回顾,以评估这种罕见的局限性淋巴瘤结外表现的治疗结果和预后因素。
确定了1978年至1986年间在PMH接受治疗的52例患者,并对其记录进行回顾性分析。分期检查显示,16例为I期,28例为II期,8例为III期或IV期疾病。5例患者按照甲状腺间变性癌治疗方案进行治疗,被排除在详细分析之外。在39例I期和II期疾病患者中,18例仅接受放疗,3例仅接受化疗,18例接受综合治疗。综合治疗主要用于肿瘤体积较大的患者。
总体5年精算生存率和病因特异性生存率分别为56%和64%。5年时总体无复发生存率为61%。在39例I期和II期疾病患者中,5年精算生存率、病因特异性生存率和无复发生存率分别为64%、73%和66%。单纯放疗组和综合治疗组的治疗结果无显著差异(病因特异性生存率:p = 0.25,复发率:p = 0.06)。单因素分析显示,唯一具有统计学意义的变量是肿瘤体积。年龄接近显著水平,而分期和组织学无统计学意义,可能是由于这些变量中患者分布相当均匀。初始治疗后淋巴瘤进展或复发的患者常死于该疾病。3例出现孤立性胃肠道复发,占所有复发的27%。
基于上述结果,我们认识到大多数局限性甲状腺淋巴瘤患者需要综合治疗,我们仅建议一小部分经过挑选的I期疾病且肿瘤体积小的患者单独接受放疗。