Philip T, Biron P, Philip I, Favrot M, Souillet G, Philippe N, Hervé P, Plouvier E, Bernard J L, Raybaud C
IARC Sci Publ. 1985(60):419-34.
During 1980-1983, two major advances were made in the treatment of Burkitt's lymphoma (BL): conventional but aggressive chemotherapy raised the overall survival rate from 42% with the SFOP1 protocol, COPAD, to 80% with SFOP protocols LMB 01 and 02; and massive chemotherapy followed by autologous bone-marrow transplantation (ABMT) enabled 40% of relapses to be cured. Ten patients included in the COPAD protocol were treated with massive therapy: seven because of relapse, one because of partial remission after two months' induction therapy and two because of long delay before first complete remission (CR). The therapy used was bischloroethyl nitrosourea, cytosine arabinoside, cyclophosphamide (CPM) and 6-thioguanine (BACT) in nine cases and CPM in one. The response rate was 100%, and disease-free survival was reached in five of ten cases, including four with no evidence of disease for over two years. In nine of ten patients who received ABMT, the bone marrow (BM) was not decontaminated, and BM involvement was found at death prior to day 86 from ABMT in four of five failures. Clinical and cytological analyses led to no firm conclusion about the role, if any, of reinjected BM in this outcome: a liquid-culture monitoring system used in six cases showed BM malignant cells present in the graft in one early relapse and absent in two relapses in which BACT failed; in three long-term survivors, no malignant cell was found in the graft. This first group of ten showed the efficiency of BACT and the necessity of purging BM in at least some cases before ABMT. Of the second group, selected from 43 patients given LMB 01 and 02 protocols, eight were treated by massive therapy and ABMT: one with localized stages I and II disease, four with stage III and three with stage IV. These patients received massive therapy either because of early relapse, progressive disease, partial remission after induction therapy or long delay before CR, or as a consolidation of CR in cases of central nervous system or cerebrospinal fluid involvement. In this group, four of eight are disease-free; three of them had normal BM by in-vitro liquid-culture monitoring; their BM was not decontaminated and they had no BM relapses. In the other five cases, BM was decontaminated by Asta Z in one and by y-29/55 antibody in four.(ABSTRACT TRUNCATED AT 400 WORDS)
1980年至1983年期间,伯基特淋巴瘤(BL)的治疗取得了两项重大进展:传统但积极的化疗使总体生存率从采用SFOP1方案(COPAD)时的42%提高到采用SFOP方案LMB 01和02时的80%;大剂量化疗后进行自体骨髓移植(ABMT)使40%的复发患者得以治愈。纳入COPAD方案的10例患者接受了大剂量治疗:7例因复发,1例因诱导治疗两个月后部分缓解,2例因首次完全缓解(CR)前长期延迟。9例患者采用的治疗方案为双氯乙基亚硝脲、阿糖胞苷、环磷酰胺(CPM)和6-硫鸟嘌呤(BACT),1例采用CPM。缓解率为100%,10例患者中有5例实现无病生存,其中4例两年多无疾病证据。接受ABMT的10例患者中有9例未进行骨髓净化,5例移植失败患者中有4例在ABMT后第86天前死亡时发现有骨髓受累。临床和细胞学分析未能就回输的骨髓在这一结果中所起的作用(如果有)得出明确结论:6例患者使用的液体培养监测系统显示,1例早期复发患者的移植物中存在骨髓恶性细胞,2例BACT治疗失败的复发患者中未发现;3例长期存活者的移植物中未发现恶性细胞。这首批10例患者显示了BACT的有效性以及至少在某些情况下ABMT前净化骨髓的必要性。第二批患者从43例接受LMB 01和02方案治疗的患者中挑选,8例接受了大剂量治疗和ABMT:1例为局限性I期和II期疾病,4例为III期,3例为IV期。这些患者接受大剂量治疗的原因包括早期复发、疾病进展、诱导治疗后部分缓解或CR前长期延迟,或在中枢神经系统或脑脊液受累的情况下作为CR的巩固治疗。该组8例患者中有4例无病生存;其中3例经体外液体培养监测骨髓正常;他们未进行骨髓净化,也没有骨髓复发。在其他5例患者中,1例采用Asta Z进行骨髓净化,4例采用γ-29/55抗体进行骨髓净化。(摘要截选至400字)