López R, Martino R, Brunet S, Sureda A, Domingo-Albós A, Sierra J
Servei d'Hematologia Clínica, Hospital de la Santa Creu i Sant Pau, Av. Sant Antoni Maria Claret, 167, 08025 Barcelona, Spain.
Haematologica. 1999 Oct;84(10):911-6.
Patients with follicular lymphoma (FL) who do not respond to first-line chemotherapy or those who relapse after obtaining a remission have a poor outcome with standard treatment. In an effort to obtain a high rate of responses we designed an intensive brief duration salvage chemotherapy regimen.
Forty-four consecutive patients with advanced follicular lymphoma were treated. Nine had primary refractory disease, 13 had achieved a partial remission, 16 were in untreated relapse or progression and six were in chemosensitive relapse. The IAPVP-16 regimen consists in ifosfamide 5 g/m(2) iv on day 1, etoposide 100 mg/m(2) iv on days 1-3, Ara-C 1.2 g/m(2)/12 hours iv on days 1-2 and methylprednisolone, 80 mg/m(2) iv on days 1-5. Granulocyte colony-stimulating factor was used from day 6 in 68 of 114 courses.
Eighteen patients (41%) achieved a complete remission and 17 (39%) a partial remission, for an overall response rate of 80%. There were no treatment-related deaths. All treatment courses were followed by severe neutropenia, and 66% also by severe thrombocytopenia, but there were no serious hemorrhagic events. Neutropenic fever occurred in 56% of the courses with only four severe infections. Non-hematologic toxicity was modest. Twenty-eight patients proceeded to a stem cell transplantation. After a median follow-up of 25 months (range 4-95), the median progression-free survival and overall survival are 32 and 58 months, respectively. The median PFS was 33 months for responders and 11 months for non-responders (p=0.05), while the median OS has not been reached in responders and is 23 months in non-responders (p=0.0005).
. The IAPVP-16 regimen is an effective and well tolerated treatment for advanced FL, allowing most eligible patients to proceed with significant tumor reduction to high-dose therapy and SCT.
对一线化疗无反应或缓解后复发的滤泡性淋巴瘤(FL)患者,采用标准治疗预后较差。为了获得较高的缓解率,我们设计了一种强化短疗程挽救性化疗方案。
连续治疗44例晚期滤泡性淋巴瘤患者。9例为原发性难治性疾病,13例达到部分缓解,16例为未经治疗的复发或进展期患者,6例为化疗敏感复发患者。IAPVP - 16方案包括:第1天静脉注射异环磷酰胺5 g/m²,第1 - 3天静脉注射依托泊苷100 mg/m²,第1 - 2天每12小时静脉注射阿糖胞苷1.2 g/m²,第1 - 5天静脉注射甲泼尼龙80 mg/m²。114个疗程中有68个疗程从第6天开始使用粒细胞集落刺激因子。
18例患者(41%)达到完全缓解,17例(39%)达到部分缓解,总缓解率为80%。无治疗相关死亡。所有治疗疗程均出现严重中性粒细胞减少,66%的疗程还出现严重血小板减少,但无严重出血事件。56%的疗程出现中性粒细胞减少性发热,仅4例严重感染。非血液学毒性较轻。28例患者进行了干细胞移植。中位随访25个月(范围4 - 95个月)后,无进展生存期和总生存期的中位数分别为32个月和58个月。缓解者的无进展生存期中位数为33个月,未缓解者为11个月(p = 0.05),缓解者的总生存期中位数未达到,未缓解者为23个月(p = 0.0005)。
IAPVP - 16方案是一种治疗晚期FL有效的且耐受性良好的治疗方法,能使大多数符合条件的患者在进行高剂量治疗和自体造血干细胞移植前显著降低肿瘤负荷。