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Incidence of therapy-related myeloid neoplasia after initial therapy for chronic lymphocytic leukemia with fludarabine-cyclophosphamide versus fludarabine: long-term follow-up of US Intergroup Study E2997

机译:氟达拉滨-环磷酰胺与氟达拉滨对慢性淋巴细胞白血病初次治疗后与治疗相关的髓样瘤形成的发生率:美国小组研究E2997的长期随访

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摘要

Chemotherapy-related myeloid neoplasia (t-MN) is a significant late toxicity concern after cancer therapy. In the randomized intergroup phase 3 E2997 trial, initial therapy of chronic lymphocytic leukemia with fludarabine plus cyclophosphamide (FC) compared with fludarabine alone yielded higher complete and overall response rates and longer progression-free, but not overall, survival. Here, we report t-MN incidence in 278 patients enrolled in E2997 with a median 6.4-year follow-up. Thirteen cases (4.7%) of t-MN occurred at a median of 5 years from initial therapy for chronic lymphocytic leukemia, 9 after FC and 4 after fludarabine alone. By cumulative incidence methodology, rates of t-MN at 7 years were 8.2% after FC and 4.6% after fludarabine alone (P = .09). Seven of the 9 cases of t-MN after FC occurred without additional therapy. Abnormalities involving chromosomes 5 or 7 were found in 10 cases, which suggests alkylator involvement. These data suggest that FC may induce more t-MN than fludarabine alone.
机译:化疗相关的骨髓瘤形成(t-MN)是癌症治疗后重要的晚期毒性问题。在3组E2997组间随机试验中,与单独使用氟达拉滨相比,氟达拉滨加环磷酰胺(FC)的慢性淋巴细胞白血病的初始治疗产生了更高的完全和总体缓解率,并且无进展生存期更长,但并非总生存期更长。在这里,我们报告了278位E2997入组患者的t-MN发生率,中位随访时间为6.4年。慢性淋巴细胞性白血病最初治疗开始的中位时间为5年,其中13例(4.7%)t-MN发生在FC后9例,仅氟达拉滨后4例。通过累积发病率方法,仅使用氟达拉滨后7年的t-MN发生率分别为FC后的8.2%和4.6%(P = .09)。 FC后9例t-MN中有7例未进行额外治疗。在10例病例中发现了涉及5号或7号染色体的异常,这表明有烷基化子参与。这些数据表明,FC可能比单独的氟达拉滨诱导更多的t-MN。

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