Eifel P J, Cassady J R, Belli J A
Int J Radiat Oncol Biol Phys. 1987 Jun;13(6):847-52. doi: 10.1016/0360-3016(87)90098-8.
Between 1971 and 1981, 79 previously untreated children with proven or presumed gliomas of the brainstem or midbrain were seen and treated at the Joint Center for Radiation Therapy and Children's Hospital Medical Center in Boston. Twenty-seven patients had tumors of the thalamus and midbrain (Group I) and 52 had lesions of the pons or medulla (Group II). Overall 5- and 10-year survivals were 50% and 41% respectively. Eighty percent of deaths occurred within 2 years of treatment. Eighty-six percent of the children (69/79) had clinical improvement or stabilization of disease after treatment. Group I patients had a 5-year survival of 73% which was significantly greater than that of Group II patients (38%) (p = 0.007). Children who presented with hypothalamic tumors in association with a diencephalic syndrome or other growth abnormality appeared to have had a better prognosis with 6/6 (100%) surviving without evidence of disease. Age at presentation was not correlated with prognosis. Of 10 children less than 3 years of age at presentation and treatment, 6 are alive (60%) at 2, 3, 7, 9, 10, and 12 years after treatment. The functional results in this group have been good--all six are leading apparently normal lives in regular schools with minor or no apparent neurologic deficits. Although these children will require long term follow-up to determine whether cures have actually been achieved, it appears that the majority achieve some benefit, that a significant proportion enjoy long term survival, and that very young children may be treated successfully with minimal radiation-induced neurologic sequela.
1971年至1981年间,波士顿放射治疗联合中心和儿童医院医疗中心诊治了79名先前未经治疗、经证实或疑似患有脑干或中脑胶质瘤的儿童。27例患者患有丘脑和中脑肿瘤(第一组),52例患有脑桥或延髓病变(第二组)。总体5年和10年生存率分别为50%和41%。80%的死亡发生在治疗后2年内。86%的儿童(69/79)在治疗后病情有临床改善或稳定。第一组患者的5年生存率为73%,显著高于第二组患者(38%)(p = 0.007)。出现下丘脑肿瘤并伴有间脑综合征或其他生长异常的儿童预后似乎较好,6/6(100%)存活且无疾病迹象。发病年龄与预后无关。在10名发病和治疗时年龄小于3岁的儿童中,6名在治疗后2、3、7、9、10和12年时存活(60%)。该组的功能结果良好——所有6名儿童在正规学校过着明显正常的生活,只有轻微或无明显神经功能缺损。尽管这些儿童需要长期随访以确定是否真正治愈,但似乎大多数儿童都获得了一定益处,相当一部分儿童长期存活,并且非常年幼的儿童可以通过最小化的辐射诱发神经后遗症成功治疗。