Ansell Stephen M, Ristow Kay M, Habermann Thomas M, Wiseman Gregory A, Witzig Thomas E
Divisions of Hematology and Nuclear Medicine, Mayo Clinic, Rochester, MN 55905, USA.
J Clin Oncol. 2002 Sep 15;20(18):3885-90. doi: 10.1200/JCO.2002.10.143.
Yttrium-90 (90Y) ibritumomab tiuxetan (Zevalin; IDEC Pharmaceutical, San Diego, CA) is an effective therapy for patients with relapsed B-cell non-Hodgkin's lymphoma. The predominant toxicity of 90Y ibritumomab tiuxetan has been myelosuppression, and concern has been expressed about the tolerability of further treatment after this therapy. The goal of this analysis was to evaluate the therapy given to patients who relapsed after 90Y ibritumomab tiuxetan.
A retrospective analysis was performed on 58 patients treated at a single institution on five separate protocols that used 90Y ibritumomab tiuxetan 0.4 mCi/kg. All patients had experienced disease progression after 90Y ibritumomab tiuxetan treatment and received subsequent therapy. The toxicity seen in this cohort of patients with subsequent treatment regimens was analyzed and compared with that of control groups who did not receive 90Y ibritumomab tiuxetan.
The median number of subsequent therapies was two (range, one to seven). Sixteen (28%) of the 58 patients received growth factor support with subsequent chemotherapy, and two patients were treated with reduced doses because of persistent pancytopenia. Eight patients subsequently had an autologous stem-cell transplantation with stem cells collected after 90Y ibritumomab tiuxetan therapy. Excluding patients hospitalized at the time of transplantation, 13 patients were hospitalized for neutropenic fever, thrombocytopenia, or both. When compared to patients who did not receive 90Y ibritumomab tiuxetan, there was no significant difference in toxicity.
We conclude that chemotherapy or autologous stem-cell transplantation after prior therapy with 90Y ibritumomab tiuxetan is feasible and reasonably well tolerated. The toxicity with subsequent therapy seems similar to that in patients not treated with 90Y ibritumomab tiuxetan.
钇-90(90Y)替伊莫单抗(泽瓦林;IDEC制药公司,加利福尼亚州圣地亚哥)是复发的B细胞非霍奇金淋巴瘤患者的一种有效治疗方法。90Y替伊莫单抗的主要毒性为骨髓抑制,人们对该治疗后进一步治疗的耐受性表示担忧。本分析的目的是评估90Y替伊莫单抗治疗后复发患者所接受的治疗。
对在单一机构按照五个不同方案接受治疗的58例患者进行回顾性分析,这些方案使用0.4mCi/kg的90Y替伊莫单抗。所有患者在90Y替伊莫单抗治疗后均出现疾病进展并接受了后续治疗。分析该组接受后续治疗方案患者中观察到的毒性,并与未接受90Y替伊莫单抗的对照组进行比较。
后续治疗的中位数为两次(范围为一至七次)。58例患者中有16例(28%)在后续化疗时接受了生长因子支持,2例患者因持续性全血细胞减少而接受了减量治疗。8例患者随后进行了自体干细胞移植,其干细胞是在90Y替伊莫单抗治疗后采集的。排除移植时住院的患者,13例患者因中性粒细胞减少性发热、血小板减少或两者而住院。与未接受90Y替伊莫单抗的患者相比,毒性无显著差异。
我们得出结论,先前接受90Y替伊莫单抗治疗后进行化疗或自体干细胞移植是可行的,且耐受性相当良好。后续治疗的毒性似乎与未接受90Y替伊莫单抗治疗的患者相似。