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首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Rituximab, gemcitabine and oxaliplatin: an effective salvage regimen for patients with relapsed or refractory B-cell lymphoma not candidates for high-dose therapy.
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Rituximab, gemcitabine and oxaliplatin: an effective salvage regimen for patients with relapsed or refractory B-cell lymphoma not candidates for high-dose therapy.

机译:利妥昔单抗,吉西他滨和奥沙利铂:对于复发或难治性B细胞淋巴瘤而不适合大剂量治疗的患者,有效的治疗方案。

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BACKGROUND: High-dose therapy (HDT) with stem-cell support is the reference treatment for relapsed lymphoma, but is not appropriate for all patients. Conventional salvage chemotherapies have been used with limited efficacy and significant toxicity. Rituximab, gemcitabine and oxaliplatin are active as single agents in relapsed or refractory lymphoma, and have demonstrated synergistic effects in vitro and in vivo. PATIENTS AND METHODS: Forty-six patients with relapsed or refractory B-cell lymphoma received up to eight cycles of R-GemOx (rituximab 375 mg/m(2) on day 1, gemcitabine 1000 mg/m(2) and oxaliplatin 100 mg/m(2) on day 2). The majority (72%) had diffuse large B-cell lymphoma. RESULTS: After four cycles of R-GemOx, the overall response rate was 83% [50% complete response (CR)/unconfirmed CR (CRu)]. High CR/CRu rates were observed in all histological subtypes. In patients who had previously received rituximab, the CR/CRu rate after eight cycles was 65%. The 2-year event-free and overall survival rates (median follow-up of 28 months) were 43% and 66%, respectively. Among responders, the probability of being disease free for 2 years was 62%. Treatment was generally well tolerated. CONCLUSION: R-GemOx shows promising activity with acceptable toxicity in patients with relapsed/refractory B-cell lymphoma who are not eligible for HDT.
机译:背景:采用干细胞支持的大剂量疗法(HDT)是复发性淋巴瘤的参考疗法,但并不适合所有患者。使用常规的抢救化学疗法具有有限的功效和明显的毒性。利妥昔单抗,吉西他滨和奥沙利铂在复发或难治性淋巴瘤中作为单一药物具有活性,并已在体外和体内显示出协同作用。患者和方法:46例复发性或难治性B细胞淋巴瘤患者在第1天接受了多达8个周期的R-GemOx(利妥昔单抗375 mg / m(2),吉西他滨1000 mg / m(2)和奥沙利铂100 mg / m(2)在第2天)。大多数(72%)患有弥漫性大B细胞淋巴瘤。结果:经过四个周期的R-GemOx,总缓解率为83%[50%完全缓解(CR)/未经证实的CR(CRu)]。在所有组织学亚型中均观察到高CR / CRu率。在先前接受利妥昔单抗的患者中,八个周期后的CR / CRu率为65%。两年无事件生存率和总生存率(中位随访28个月)分别为43%和66%。在响应者中,2年内无疾病的可能性为62%。治疗通常耐受良好。结论:R-GemOx在不适合HDT的复发性/难治性B细胞淋巴瘤患者中显示出令人鼓舞的活性和可接受的毒性。

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