Patte C, Philip T, Rodary C, Zucker J M, Behrendt H, Gentet J C, Lamagnère J P, Otten J, Dufillot D, Pein F
Department of Pediatrics, Institut Gustave-Roussy, Villejuif, France.
J Clin Oncol. 1991 Jan;9(1):123-32. doi: 10.1200/JCO.1991.9.1.123.
From April 1984 to December 1987, the French Pediatric Oncology Society (SFOP) organized a randomized trial for advanced-stage B-cell lymphoma without CNS involvement to study the possibility of reducing the length of treatment to 4 months. After receiving the same three intensive six-drug induction courses based on high-dose fractionated cyclophosphamide, high-dose methotrexate (HD MTX), and cytarabine in continuous infusion, patients were evaluated for remission. Those who achieved complete remission (CR) were randomized between a long arm (five additional courses with two additional drugs; 16 weeks of treatment) and a short arm (two additional courses; 5 weeks). For patients in partial remission (PR), intensification of treatment was indicated. Two hundred sixteen patients were registered: 15 stage II nasopharyngeal and extensive facial tumors, 167 stage III, and 34 stage IV, 20 of the latter having more than 25% blast cells in bone marrow. The primary sites of involvement were abdomen in 172, head and neck in 30, thorax in two, and other sites in 12. One hundred sixty-seven patients are alive in first CR with a minimum follow-up of 18 months; four are lost to follow-up. Eight patients died from initial treatment failure, 14 died from toxicity or deaths unrelated to tumor or treatment, and 27 relapsed. The event-free survival (EFS), with a median follow-up of 38 months, is 78% (SE 3) for all the patients, 73% (SE 11) for the stage II patients, 80% (SE 3) for the stage III patients, and 68% (SE 8) for the stage IV and acute lymphoblastic leukemia (ALL) patients. One hundred sixty-six patients were randomized: 82 in the short arm and 84 in the long arm. EFS is, respectively, 89% and 87%. Statistical analysis confirms equivalence of both treatment arms with regard to EFS. Moreover, morbidity was lower in the short arm. This study confirms the high survival rate obtained in the previous LMB 0281 study without radiotherapy or debulking surgery and demonstrates the effectiveness of short treatment.
1984年4月至1987年12月,法国儿科肿瘤学会(SFOP)组织了一项针对无中枢神经系统受累的晚期B细胞淋巴瘤的随机试验,以研究将治疗时长缩短至4个月的可能性。在接受基于大剂量分次环磷酰胺、大剂量甲氨蝶呤(HD MTX)和持续输注阿糖胞苷的相同三个强化六药诱导疗程后,对患者进行缓解评估。达到完全缓解(CR)的患者被随机分为长疗程组(再进行五个疗程并加用两种药物;治疗16周)和短疗程组(再进行两个疗程;治疗5周)。对于部分缓解(PR)的患者,则需强化治疗。共登记了216例患者:15例为II期鼻咽癌和广泛面部肿瘤,167例为III期,34例为IV期,其中20例IV期患者骨髓中原始细胞超过25%。受累的主要部位为腹部172例,头颈部30例,胸部2例,其他部位12例。167例患者处于首次CR存活状态,最短随访18个月;4例失访。8例死于初始治疗失败,14例死于毒性反应或与肿瘤或治疗无关的死亡,27例复发。所有患者的无事件生存率(EFS),中位随访38个月,为78%(标准误3),II期患者为73%(标准误11),III期患者为80%(标准误3),IV期和急性淋巴细胞白血病(ALL)患者为68%(标准误8)。166例患者被随机分组:短疗程组82例,长疗程组84例。EFS分别为89%和87%。统计分析证实两个治疗组在EFS方面具有等效性。此外,短疗程组的发病率较低。本研究证实了在之前的LMB 0281研究中在未进行放疗或减瘤手术的情况下所获得的高生存率,并证明了短疗程治疗的有效性。