Fox Chase Cancer Center, Philadelphia, PA, USA.
Blood. 2011 Sep 29;118(13):3525-7. doi: 10.1182/blood-2011-03-342485. Epub 2011 Jul 29.
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.
化疗相关髓系肿瘤(t-MN)是癌症治疗后一个重要的迟发性毒性问题。在随机分组、多中心的 3 期 E2997 临床试验中,与单用氟达拉滨相比,氟达拉滨联合环磷酰胺(FC)初始治疗慢性淋巴细胞白血病可提高完全缓解率和总缓解率、延长无进展生存期,但不能延长总生存期。在此,我们报告了中位随访时间为 6.4 年的 E2997 试验中 278 例患者的 t-MN 发生率。在初始慢性淋巴细胞白血病治疗后 5 年时,13 例(4.7%)患者发生 t-MN,9 例在 FC 后发生,4 例在单用氟达拉滨后发生。采用累积发生率方法,FC 组 7 年时 t-MN 的发生率为 8.2%,而单用氟达拉滨组为 4.6%(P=0.09)。FC 组 9 例 t-MN 中有 7 例未接受额外治疗。10 例患者发现涉及 5 号或 7 号染色体的异常,提示烷化剂参与。这些数据表明,FC 引起的 t-MN 可能多于单用氟达拉滨。