Velasquez William S, Lew Danika, Grogan Thomas M, Spiridonidis C Harris, Balcerzak Stanley P, Dakhil Shaker R, Miller Thomas P, Lanier Keith S, Chapman Robert A, Fisher Richard I
University of Texas Medical Branch, Galveston, USA.
J Clin Oncol. 2003 May 15;21(10):1996-2003. doi: 10.1200/JCO.2003.09.047.
To determine the efficacy of combination fludarabine and mitoxantrone (FN) in untreated stages III and IV low-grade lymphoma. The major end point was to estimate progression-free survival (PFS) in all eligible patients.
Seventy-eight eligible patients were registered. Chemotherapy courses were administered every 4 weeks with mitoxantrone 10 mg/m2 on day 1 and fludarabine 25 mg/m2 on days 1, 2, and 3 for a total of six to eight cycles. Pneumocystis carinii prophylaxis was required.
Seventy-three patients (94%) attained an objective response. Complete remission was demonstrated in 34 patients (44%) and partial remission was demonstrated in 39 patients (50%). With a median follow-up time of 5.5 years, the median PFS was 32 months, with a 4-year PFS rate of 38%. Median survival has not been reached and 88% of all patients are alive at 4 years. The application of the International Prognostic Index and serologic staging showed significant differences in PFS in all risk groups, whereas overall survival was markedly worse for the highest-risk group in either prognostic model. Three prior Southwest Oncology Group trials using a regimen of cyclophosphamide, doxorubicin, vincristine, and prednisone or a combination of prednisone, vincristine, methotrexate, cytarabine, cyclophosphamide, etoposide, nitrogen mustard, vincristine, procarbazine, and prednisone in similar patient populations demonstrated comparable clinical outcome, although the 4-year survival for FN was better. FN was well tolerated, but mild to severe reversible myelosuppression was noted. Other complications were rare.
FN is an effective, safe chemotherapy combination for patients with advanced-stage, low-grade lymphoma. Clinical outcomes were comparable to prior published data using anthracycline-based regimens.
确定氟达拉滨与米托蒽醌联合方案(FN)用于未经治疗的Ⅲ期和Ⅳ期低度淋巴瘤的疗效。主要终点是评估所有符合条件患者的无进展生存期(PFS)。
登记了78例符合条件的患者。化疗疗程每4周进行一次,第1天给予米托蒽醌10 mg/m²,第1、2、3天给予氟达拉滨25 mg/m²,共进行6至8个周期。需要进行卡氏肺孢子虫预防。
73例患者(94%)获得客观缓解。34例患者(44%)达到完全缓解,39例患者(50%)达到部分缓解。中位随访时间为5.5年,中位PFS为32个月,4年PFS率为38%。中位生存期尚未达到,4年时88%的患者仍存活。国际预后指数和血清学分期的应用显示,所有风险组的PFS存在显著差异,而在任何一种预后模型中,最高风险组的总生存期明显更差。西南肿瘤学组之前的三项试验在类似患者群体中使用环磷酰胺、阿霉素、长春新碱和泼尼松方案或泼尼松、长春新碱、甲氨蝶呤、阿糖胞苷、环磷酰胺、依托泊苷、氮芥、长春新碱、丙卡巴肼和泼尼松联合方案,显示出相当的临床结果,尽管FN方案的4年生存率更高。FN耐受性良好,但注意到有轻度至重度的可逆性骨髓抑制。其他并发症罕见。
FN是晚期低度淋巴瘤患者一种有效、安全的化疗联合方案。临床结果与之前发表的使用含蒽环类药物方案的数据相当。