Jenkin R D, Anderson J R, Chilcote R R, Coccia P F, Exelby P R, Kersey J H, Kushner J H, Meadows A T, Siegel S E, Sposto R
J Clin Oncol. 1984 Feb;2(2):88-97. doi: 10.1200/JCO.1984.2.2.88.
Investigators of the Children's Cancer Study Group entered 73 children with previously untreated localized non-Hodgkin's lymphoma on a prospective randomized trial of systemic treatment with either a four-drug program (cyclophosphamide, vincristine, methotrexate, prednisone [COMP]) or a 10-drug (LSA2-L2 modified) program of 18 months duration. All patients received central nervous system prophylaxis with intrathecal methotrexate and most received local or regional radiation treatment. The three-year relapse-free survival rate for all patients (N = 73) was 84%; for COMP (N = 42) was 85%, and for LSA2-L2 (N = 31) was 84%. Of the 12 patients who suffered adverse events eight relapsed and four died of toxicity. Histopathology was reviewed centrally. Of 32 patients with nonlymphoblastic disease treated with COMP only one relapsed. Of 26 patients treated with LSA2-L2, four relapsed. Patients with localized lymphoblastic disease were uncommon. None of three patients treated with LSA2-L2 relapsed compared with three of nine treated with COMP. COMP is an excellent treatment for patients with localized disease of nonlymphoblastic type, but the relative value of the two regimens for patients with localized lymphoblastic disease is uncertain.
儿童癌症研究组的研究人员让73名先前未经治疗的局限性非霍奇金淋巴瘤患儿参与一项前瞻性随机试验,该试验采用四种药物方案(环磷酰胺、长春新碱、甲氨蝶呤、泼尼松[COMP])或为期18个月的十种药物(改良的LSA2-L2)方案进行全身治疗。所有患者均接受鞘内注射甲氨蝶呤进行中枢神经系统预防,大多数患者接受局部或区域放射治疗。所有患者(N = 73)的三年无复发生存率为84%;COMP组(N = 42)为85%,LSA2-L2组(N = 31)为84%。在12名出现不良事件的患者中,8名复发,4名死于毒性反应。组织病理学由中心进行复查。在仅接受COMP治疗的32例非淋巴细胞性疾病患者中,只有1例复发。在接受LSA2-L2治疗的26例患者中,4例复发。局限性淋巴细胞性疾病患者并不常见。接受LSA2-L2治疗的3例患者均未复发,而接受COMP治疗的9例患者中有3例复发。COMP是治疗非淋巴细胞性类型局限性疾病患者的一种优秀疗法,但对于局限性淋巴细胞性疾病患者,这两种方案的相对价值尚不确定。