Pan Dorothy, Qin Jing, Farber Charles, O'Brien James, Filippa Daniel, Portlock Carol S
Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Leuk Lymphoma. 2003 Jun;44(6):967-71. doi: 10.1080/1042819031000067710.
The role of high dose therapy, including autologous stem cell transplantation (ASCT) in indolent non-Hodgkin's lymphomas remains controversial. We evaluated a dose intense regimen of CHOP induction followed by high dose cyclophosphamide consolidation (CHOP-HC) versus CHOP alone in a prospective comparison to assess intensified therapy without ASCT. Twenty-five patients with previously untreated advanced stage indolent NHL were enrolled: follicular lymphoma, grade 1 (11 patients) and grade 2 (8 patients); small lymphocytic lymphoma (5 patients); and lymphoplasmacytic lymphoma (1 patient). All patients were treated as clinically indicated. The median age was 47 years (21-70). There were 15 males, and 10 females. Three patients had intra-abdominal stage II, 2 patients with stage III, and 20 patients with stage IV disease. All patients received induction with CHOP for 4 cycles (weeks 1, 4, 7, 10): cyclophosphamide 750 mg/m2 i.v., doxorubicin 50 mg/m2 i.v., vincristine 1.4 mg/m2 i.v. (2 mg capped dose) and prednisone 100 mg p.o. x 5 days. Following induction, responding patients were given consolidation with either high dose cyclophosphamide @ 3 gm/m2 i.v. for 3 doses with G-CSF (weeks 13, 15, 17) or 2 additional cycles of CHOP (weeks 13, 16), stratified by stage and bulk of disease. The overall response rate to CHOP was 92% (3 CR, 8 PR) and to CHOP-HC was 93% (4 CR, 8 PR). The overall response, complete response and partial response rates were comparable in both arms. Median progression free survival for CHOP was 15.9 and 23.0 months for CHOP-HC. At 74.3 months median follow-up, all patients in the CHOP arm have recurred; 3 patients in the CHOP-HC arm (3 CR) have not recurred. The median overall survival has not been reached (at 5 years, 77% OS for CHOP-HC versus 83% OS for CHOP alone]. Greater hematologic toxicity was observed with CHOP-HC resulting in an increased number of hospitalizations for sepsis. There were no treatment-related deaths. No myelodysplasia or acute leukemia has been seen to date. With no obvious improvement in CR and with greater hematologic toxicity than CHOP, CHOP-HC is not recommended for treatment of indolent non-Hodgkin's lymphomas.
大剂量疗法,包括自体干细胞移植(ASCT)在惰性非霍奇金淋巴瘤中的作用仍存在争议。我们前瞻性比较了CHOP诱导方案后序贯大剂量环磷酰胺巩固治疗(CHOP-HC)与单纯CHOP方案,以评估不进行ASCT的强化治疗。纳入25例既往未经治疗的晚期惰性非霍奇金淋巴瘤患者:1级滤泡性淋巴瘤(11例)、2级滤泡性淋巴瘤(8例)、小淋巴细胞淋巴瘤(5例)和淋巴浆细胞淋巴瘤(1例)。所有患者均根据临床指征进行治疗。中位年龄为47岁(21-70岁)。男性15例,女性10例。3例患者为腹腔内II期,2例为III期,20例为IV期疾病。所有患者接受CHOP诱导治疗4个周期(第1、4、7、10周):环磷酰胺750mg/m²静脉注射、阿霉素50mg/m²静脉注射、长春新碱1.4mg/m²静脉注射(最大剂量2mg)及泼尼松100mg口服,共5天。诱导治疗后,根据疾病分期和肿块大小将缓解的患者分层,分别给予大剂量环磷酰胺3g/m²静脉注射,共3剂,同时给予粒细胞集落刺激因子(第13、15、17周)或额外2个周期的CHOP方案(第13、16周)进行巩固治疗。CHOP方案的总缓解率为92%(3例完全缓解,8例部分缓解),CHOP-HC方案的总缓解率为93%(4例完全缓解,8例部分缓解)。两组的总缓解率、完全缓解率和部分缓解率相当。CHOP方案的中位无进展生存期为15.9个月,CHOP-HC方案为23.0个月。中位随访74.3个月时,CHOP组所有患者均复发;CHOP-HC组3例完全缓解患者未复发。中位总生存期尚未达到(5年时,CHOP-HC组总生存率为77%,单纯CHOP组为83%)。CHOP-HC方案观察到更大的血液学毒性,导致脓毒症住院人数增加。无治疗相关死亡。迄今为止未观察到骨髓发育异常或急性白血病。由于完全缓解无明显改善且血液学毒性大于CHOP方案效应,不推荐CHOP-HC方案用于治疗惰性非霍奇金淋巴瘤。