Anger B, Bunjes D, Carbonell F, Kurrle E, Heimpel H
Blut. 1986 Oct;53(4):279-86. doi: 10.1007/BF00320885.
From 6/79 until 2/86, 9 patients (median age 39) with Burkitt's lymphoma were treated. Stage D disease was seen in 7 cases, stage C in two and stage A in one. The main symptom was abdominal pain or a rapidly progressing abdominal tumor. Three patients had bone marrow involvement and two had a Burkitt's leukemia. Three had typical chromosomal aberrations. Therapy consisted of a variety of chemotherapy regimens plus additional radiotherapy and/or bulk surgery. Two patients achieved complete remissions (of 6 and 20+ months duration), and 4 partial remissions were obtained. The remaining patients had either progressive, drug resistant disease or died early. One patient is currently alive and in complete remission at 20+ months. A second patient is alive at 20+ months in partial remission with traces of IgM-paraprotein still detectable. The main causes of death were tumor-lysis syndrome (4 patients) and therapy related sepsis with progressive tumor (3 patients). This poor outcome is probably due to a high proportion of high-risk patients and suboptimal therapy for this rapidly proliferating tumor.
从1979年6月至1986年2月,对9例(中位年龄39岁)伯基特淋巴瘤患者进行了治疗。7例为D期疾病,2例为C期,1例为A期。主要症状为腹痛或腹部肿瘤迅速进展。3例患者有骨髓受累,2例患有伯基特白血病。3例有典型的染色体畸变。治疗包括多种化疗方案加额外的放疗和/或大块手术。2例患者达到完全缓解(持续时间分别为6个月和20多个月),4例获得部分缓解。其余患者有疾病进展、耐药或早期死亡。1例患者目前存活,20多个月处于完全缓解状态。第2例患者存活20多个月,处于部分缓解状态,仍可检测到微量IgM副蛋白。主要死亡原因是肿瘤溶解综合征(4例患者)和与治疗相关的败血症伴肿瘤进展(3例患者)。这种不良结局可能是由于高危患者比例高以及对这种快速增殖肿瘤的治疗不够理想。