Ferreri A J M, Blay J Y, Reni M, Pasini F, Gubkin A, Tirelli U, Calderoni A, Zucca E, Cortelazzo S, Chassagne C, Tinguely M, Borisch B, Berger F, Ponzoni M, Cavalli F
Department of Radiochemotherapy, San Raffaele H Scientific Institute, Milan, Italy.
Ann Oncol. 2002 Apr;13(4):531-8. doi: 10.1093/annonc/mdf080.
Reported data regarding intraocular lymphoma (IOL) management are anecdotal. Cases of IOL included in an international multicentre series of 378 immunocompetent patients with primary central nervous system lymphomas (PCNSLs) were reviewed.
Staging included slit-lamp examination in 170 patients: IOL was diagnosed in 22 cases (13%). A concomitant brain lesion was detected in 21 cases. Planned treatment was chemotherapy followed by radiotherapy in 13 cases, chemotherapy alone in three and radiotherapy, followed by or not by chemotherapy in five; one patient was not treated. Chemotherapy included high-dose methotrexate in 12 cases. Ten patients received intrathecal chemotherapy. Radiotherapy consisted of whole brain irradiation, followed by or not by a tumour bed boost; ocular irradiation was planned in 15 cases. Irradiation in one patient without brain lesions was limited to the orbits only (50 Gy).
IOL was positively correlated to systemic symptoms and meningeal disease. Fifteen patients (71%) achieved an objective response; 16 patients experienced a failure (2-year failure-free survival 34+/-10%). Failures involved the eyes in eight cases, with a 2-year time to ocular relapse of 59+/-11%. Ocular failure was less common in patients treated with chemotherapy plus ocular irradiation and was associated with a significantly shorter survival. Seven patients are alive [median follow-up 53 months, 2-year overall survival (OS): 39+/-11%] , five of whom were treated with ocular irradiation. The patient with isolated IOL is alive and disease-free at 14 months. OS of the entire series was similar to that of PCNSL patients with negative slit-lamp examination.
IOL is usually associated with concomitant brain disease and shows a survival similar to that of the rest of PCNSLs. Chemotherapy combined with ocular irradiation resulted in better control of ocular disease, which seems to be associated with survival. In view of the potential role of ocular irradiation, the use of chemotherapy alone in phase II trials should be critically reconsidered in PCNSL patients with ocular disease.
关于眼内淋巴瘤(IOL)治疗的数据多为个案报道。对纳入国际多中心系列研究的378例免疫功能正常的原发性中枢神经系统淋巴瘤(PCNSL)患者中的IOL病例进行了回顾。
170例患者的分期检查包括裂隙灯检查:确诊IOL 22例(13%)。21例检测到合并脑病变。计划治疗方案为:13例先化疗后放疗,3例单纯化疗,5例先放疗,后续是否化疗不定;1例未接受治疗。12例化疗采用大剂量甲氨蝶呤。10例患者接受鞘内化疗。放疗包括全脑照射,后续是否追加瘤床野照射不定;15例计划进行眼部照射。1例无脑部病变患者的照射仅限于眼眶(50 Gy)。
IOL与全身症状和脑膜疾病呈正相关。15例患者(71%)获得客观缓解;16例患者治疗失败(2年无失败生存率34±10%)。8例患者的失败累及眼部,眼部复发的2年时间为59±11%。化疗加眼部照射治疗的患者眼部失败较少见,且与生存期明显缩短相关。7例患者存活[中位随访53个月,2年总生存率(OS):39±11%],其中5例接受了眼部照射。孤立性IOL患者在14个月时存活且无疾病。整个系列的OS与裂隙灯检查阴性的PCNSL患者相似。
IOL通常与合并脑疾病相关,生存期与其他PCNSL患者相似。化疗联合眼部照射能更好地控制眼部疾病,这似乎与生存期相关。鉴于眼部照射的潜在作用,对于有眼部疾病的PCNSL患者,在II期试验中单纯使用化疗应重新进行严格评估。