Devereux C K, Vidaver R, Hafstein M P, Zito G, Troiano R, Dowling P C, Cook S D
Department of Radiation Oncology, Clara Maass Medical Center, Belleville, NJ 07109.
Int J Radiat Oncol Biol Phys. 1988 Jan;14(1):197-203. doi: 10.1016/0360-3016(88)90068-5.
Although chemical immunosuppression has been shown to benefit patients with chronic progressive multiple sclerosis (MS), it appears that chemotherapy has an appreciable oncogenic potential in patients with multiple sclerosis. Accordingly, we developed a modified total lymphoid irradiation (TLI) regimen designed to reduce toxicity and applied it to a randomized double blind trial of TLI or sham irradiation in MS. Standard TLI regimens were modified to reduce dose to 1,980 rad, lowering the superior mantle margin to midway between the thyroid cartilage and angle of the mandible (to avert xerostomia) and the lower margin of the mantle field to the inferior margin of L1 (to reduce gastrointestinal toxicity by dividing abdominal radiation between mantle and inverted Y), limiting spinal cord dose to 1,000 rad by custom-made spine blocks in the mantle and upper 2 cm of inverted Y fields, and also protecting the left kidney even if part of the spleen were shielded. Clinical efficacy was documented by the less frequent functional scale deterioration of 20 TLI treated patients with chronic progressive MS compared to to 20 sham-irradiated progressive MS patients after 12 months (16% versus 55%, p less than 0.03), 18 months (28% versus 63%, p less than 0.03), and 24 months (44% versus 74%, N.S.). Therapeutic benefit during 3 years follow-up was related to the reduction in lymphocyte count 3 months post-irradiation (p less than 0.02). Toxicity was generally mild and transient, with no instance of xerostomia, pericarditis, herpes zoster, or need to terminate treatment in TLI patients. However, menopause was induced in 2 patients and staphylococcal pneumonia in one. Our data suggest that this modified TLI regimen has clinical efficacy and sufficiently low toxicity to make it suitable for investigative immunosuppressive treatment of patients with progressive MS or other non-malignant conditions.
尽管化学免疫抑制已被证明对慢性进行性多发性硬化症(MS)患者有益,但化疗似乎在多发性硬化症患者中具有明显的致癌潜力。因此,我们制定了一种改良的全淋巴照射(TLI)方案以降低毒性,并将其应用于MS患者接受TLI或假照射的随机双盲试验。对标准TLI方案进行了修改,将剂量降低至1980拉德,将上半腹边缘降低至甲状软骨和下颌角之间的中点(以避免口干),将腹野的下缘降低至L1的下缘(通过将腹部辐射分配在上半腹和倒Y形区域之间来降低胃肠道毒性),通过在腹野和倒Y形野的上2厘米处使用定制的脊柱铅块将脊髓剂量限制在1000拉德,并且即使部分脾脏被屏蔽也要保护左肾。与20名接受假照射的进行性MS患者相比,20名接受TLI治疗的慢性进行性MS患者在12个月(16%对55%,p小于0.03)、18个月(28%对63%,p小于0.03)和24个月(44%对74%,无统计学意义)后功能量表恶化频率较低,证明了临床疗效。3年随访期间的治疗益处与照射后3个月淋巴细胞计数的减少有关(p小于0.02)。毒性一般较轻且短暂,TLI患者中没有出现口干、心包炎、带状疱疹或需要终止治疗的情况。然而,有2名患者出现了绝经,1名患者出现了葡萄球菌肺炎。我们的数据表明,这种改良的TLI方案具有临床疗效且毒性足够低,使其适合用于对进行性MS或其他非恶性疾病患者进行研究性免疫抑制治疗。