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原发性眼眶淋巴瘤放射治疗后的局部控制和并发症:低剂量治疗的病例分析

Local control and complications after radiation therapy for primary orbital lymphoma: a case for low-dose treatment.

作者信息

Minehan K J, Martenson J A, Garrity J A, Kurtin P J, Banks P M, Chen M G, Earle J D

机构信息

Division of Radiation Oncology, Mayo Clinic, Rochester, MN 55905.

出版信息

Int J Radiat Oncol Biol Phys. 1991 Apr;20(4):791-6. doi: 10.1016/0360-3016(91)90025-y.

Abstract

Orbital involvement at the time of initial presentation is unusual in non-Hodgkin's lymphoma. In an effort to identify potential ways of improving the radiotherapeutic management of this disease, the records of 22 patients were reviewed retrospectively. All had biopsy-proven orbital non-Hodgkin's lymphoma, and the minimal, median, and maximal durations of follow-up in surviving patients were 4.8 years, 7.0 years, and 17.4 years, respectively. Permanent local control was achieved in 21 of the 22 patients (96%). Complications were scored according to a grading scheme in which grade 1 was the least significant complication and grade 4 was blindness as a result of radiation therapy. Of the 12 patients who received a radiation dose less than 35 Gy, 6 developed a grade 1 or grade 2 complication. Of the 10 patients treated with greater than or equal to 35 Gy, 6 experienced a complication, 1 of whom had a grade 4 complication resulting in blindness and another who developed a severe keratitis, which was scored as a grade 3 complication resulting in decreased visual acuity. At last follow-up, 10 patients were alive at 4.8 to 17.4 years after completion of radiation therapy, 4 had died of intercurrent disease at 3 months to 10.6 years, and 8 had died of disease at 3 months to 15.8 years. Actuarial survival for the entire group was 75% at 5 years and 48% at 10 years. Survival in patients with Stage I AE disease (lymphoma confined to orbit) at presentation was 87% at 5 years and 50% at 10 years, and survival in patients with Stage II A through Stage IV disease was 36% at 5 years and at 10 years. Primary orbital lymphoma is an indolent disease characterized by prolonged survival after radiation therapy. Excellent local control can be achieved with radiation doses of 20 Gy to 35 Gy. Higher doses may result in an increased risk of complications.

摘要

在非霍奇金淋巴瘤初次就诊时累及眼眶的情况并不常见。为了确定改善这种疾病放射治疗管理的潜在方法,对22例患者的记录进行了回顾性分析。所有患者均经活检证实患有眼眶非霍奇金淋巴瘤,存活患者的最短、中位和最长随访时间分别为4.8年、7.0年和17.4年。22例患者中有21例(96%)实现了永久性局部控制。根据分级方案对并发症进行评分,1级为最轻微的并发症,4级为放疗导致的失明。在接受辐射剂量小于35 Gy的12例患者中,6例出现1级或2级并发症。在接受大于或等于35 Gy治疗的10例患者中,6例出现并发症,其中1例出现4级并发症导致失明,另1例出现严重角膜炎,被评为3级并发症导致视力下降。在最后一次随访时,10例患者在放疗结束后4.8至17.4年存活,4例在3个月至10.6年死于并发疾病,8例在3个月至15.8年死于该疾病。整个组的5年精算生存率为75%,10年为48%。初诊时为I AE期疾病(淋巴瘤局限于眼眶)的患者5年生存率为87%,10年为50%,II A期至IV期疾病患者5年和10年生存率均为36%。原发性眼眶淋巴瘤是一种惰性疾病,其特点是放疗后生存期延长。20 Gy至35 Gy的辐射剂量可实现良好的局部控制。更高的剂量可能会增加并发症的风险。

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