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Pilot study of tandem high-dose chemotherapy and autologous stem cell transplantation with a novel combination of regimens in patients with poor risk lymphoma.

机译:高危淋巴瘤患者串联大剂量化疗和自体干细胞移植与新方案联合治疗的初步研究。

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In an effort to improve the outcome of poor-risk lymphoma patients, we evaluated a novel regimen of tandem high-dose chemotherapy (THDC) with autologous stem cell transplantation. A total of 41 patients (median age 40 years, range 15-68 years) with poor-risk non-Hodgkin's lymphoma and Hodgkin's disease were enrolled. THDC consisted of melphalan (180 mg/m2) and escalating dose mitoxantrone (30-50 mg/m2) (MMt) for the first conditioning regimen, and thiotepa (500 mg/m2), carboplatin (800 mg/m2), and escalating dose etoposide phosphate (400-850 mg/m2), (ETCb) as the second regimen. In all, 31 patients (76%) completed both transplants, with a median time between transplants of 55 days (range 26-120). The maximum tolerated dose was determined as 40 mg/m2 for mitoxantrone and 550 mg/m2 for etoposide phosphate. The overall toxic death rate was 12%. Following high-dose chemotherapy, 10 of 24 evaluable patients (42%) were in CR. The two-year overall survival and event-free survival is 67% (95% CI, 52-81%) and 45%, (95% CI, 29-61%) for the 41 patients enrolled; and 69% (95% CI, 525-586%) and 48% (95% CI, 30-67%) for the 31 patients completing both transplants. This THDC regimen is feasible but with notable toxicity in heavily pretreated patients; its role in the current treatment of high-risk lymphoma remains to be determined.
机译:为了改善低危淋巴瘤患者的预后,我们评估了采用自体干细胞移植的新型串联高剂量化疗(THDC)方案。总共招募了41位低危非霍奇金淋巴瘤和霍奇金病患者(中位年龄40岁,范围15-68岁)。 THDC由美法仑(180 mg / m2)和递增剂量的米托蒽醌(30-50 mg / m2)(MMt)组成,用于第一个调节方案,噻替帕(500 mg / m2),卡铂(800 mg / m2)并逐步递增第二种方案是使用依托泊苷磷酸盐(400-850 mg / m2)(ETCb)。共有31例患者(76%)完成了两次移植,两次移植之间的中位时间为55天(范围26-120)。米托蒽醌的最大耐受剂量确定为40 mg / m2,磷酸依托泊苷的最大耐受剂量确定为550 mg / m2。总体毒性死亡率为12%。大剂量化疗后,可评估的24名患者中有10名(42%)处于CR。入组的41例患者的两年总生存率和无事件生存率分别为67%(95%CI,52-81%)和45%(95%CI,29-61%)。完成这两次移植的31例患者分别为69%(95%CI,525-586%)和48%(95%CI,30-67%)。这种THDC方案是可行的,但对大量预处理的患者具有明显的毒性。其在当前高危淋巴瘤治疗中的作用尚待确定。

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