Stiff P J, Dahlberg S, Forman S J, McCall A R, Horning S J, Nademanee A P, Blume K G, LeBlanc M, Fisher R I
Loyola University Stritch School of Medicine, Maywood, IL, USA.
J Clin Oncol. 1998 Jan;16(1):48-55. doi: 10.1200/JCO.1998.16.1.48.
To determine the toxicity and prognosis of patients with relapsed and refractory diffuse aggressive non-Hodgkin's lymphoma (NHL) who underwent an autologous bone marrow transplant (ABMT) using augmented preparative regimens, treated in a major cooperative group setting, and to examine prognostic factors for outcome.
Ninety-four patients with either chemosensitive (50 patients) or chemoresistant (44 patients) relapse, including 22 who failed induction chemotherapy, were treated with high-dose cyclophosphamide and etoposide with total-body irradiation (TBI) (67 patients) or an augmented carmustine (BCNU), cyclophosphamide, and etoposide (BCV) preparative regimen (27 patients) and an ABMT at 16 Southwest Oncology Group (SWOG) transplant centers. All relapsing patients were required to undergo a minimum of two courses of salvage therapy to determine chemosensitivity before transplant. Overall (OS) and progression-free survival (PFS) were determined and a Cox regression model was used to assess potential prognostic variables.
Of the 94 eligible patients, there were 10 (10.6%) deaths before day 50 posttransplant because of infection (six deaths), hemorrhagic alveolitis (three deaths), or bleeding (one death). The median 3-year PFS and OS for the entire group was 33% and 44%. For those with chemosensitive disease the PFS and OS were 42% and 55%, whereas for those with chemoresistant disease the PFS and OS were 22% and 29%. The PFS and OS for those failing induction chemotherapy were 27% and 32%. The relapse rates within the first 3 years for the chemosensitive relapse, chemoresistant, and induction failure groups were 61%, 40%, and 59%, respectively. For both PFS and OS, only disease status at transplant was a significant factor in the multivariate Cox model.
These results single institutional pilot trials exploring augmented preparative regimens. Patients undergoing transplantation for resistant disease, particularly those failing induction chemotherapy, appear to have an improved prognosis as compared with reports using standard preparative regimens. Therapies other than manipulation of standard preparative regimens appear to be required to decrease relapses following autotransplantation.
确定在大型协作组环境下接受强化预处理方案自体骨髓移植(ABMT)的复发难治性弥漫性侵袭性非霍奇金淋巴瘤(NHL)患者的毒性和预后,并研究预后的相关因素。
94例化疗敏感(50例)或化疗耐药(44例)复发的患者,包括22例诱导化疗失败的患者,在16个西南肿瘤协作组(SWOG)移植中心接受了高剂量环磷酰胺和依托泊苷联合全身照射(TBI)(67例)或强化卡莫司汀(BCNU)、环磷酰胺和依托泊苷(BCV)预处理方案(27例)及ABMT治疗。所有复发患者在移植前均需接受至少两个疗程的挽救治疗以确定化疗敏感性。确定总生存期(OS)和无进展生存期(PFS),并使用Cox回归模型评估潜在的预后变量。
94例符合条件的患者中,有10例(10.6%)在移植后第50天前因感染(6例死亡)、出血性肺泡炎(3例死亡)或出血(1例死亡)死亡。整个组的3年PFS和OS中位数分别为33%和44%。化疗敏感疾病患者的PFS和OS分别为42%和55%,而化疗耐药疾病患者的PFS和OS分别为22%和29%。诱导化疗失败患者的PFS和OS分别为27%和32%。化疗敏感复发组、化疗耐药组和诱导失败组在前3年的复发率分别为61%、40%和59%。在多变量Cox模型中,对于PFS和OS,只有移植时的疾病状态是一个显著因素。
这些结果来自探索强化预处理方案的单机构试点试验。与使用标准预处理方案的报告相比,因耐药疾病接受移植的患者,尤其是诱导化疗失败的患者,似乎预后有所改善。除了调整标准预处理方案外,似乎还需要其他疗法来减少自体移植后的复发。