Benjamini Ohad, Jain Preetesh, Trinh Long, Qiao Wei, Strom Sara S, Lerner Susan, Wang Xuemei, Burger Jan, Ferrajoli Alessandra, Kantarjian Hagop, O'Brien Susan, Wierda William, Estrov Zeev, Keating Michael
Department of Leukemia.
Leuk Lymphoma. 2015 Jun;56(6):1643-50. doi: 10.3109/10428194.2014.957203. Epub 2014 Nov 19.
Patients with chronic lymphocytic leukemia (CLL) are known to have an increased incidence of second cancers, but the contribution of commonly used frontline therapies to the incidence of second cancers is unclear. We report on the characteristics, incidence, outcomes and factors associated with second cancers in 234 patients receiving fludarabine, cyclophosphamide and rituximab (FCR) based regimens in the frontline setting. The risk of second cancers was 2.38 times higher than the expected risk in the general population. Ninety-three patients (40%) had other cancers before and 66 patients (28%) after FCR. Rates of therapy related acute myeloid leukemia/myelodysplastic syndrome (t-AML/MDS) (5.1%) and Richter transformation (RT) (9%) were high, while solid tumors were not increased. Overall survival of patients with second cancers after frontline FCR was shorter (median of 4.5 years) compared to patients with and without prior cancers. Second cancer risk after frontline FCR is mainly due to high rates of t-AML/MDS and RT, and as speculated the survival of affected patients is shorter.
已知慢性淋巴细胞白血病(CLL)患者发生第二种癌症的发生率会增加,但常用的一线疗法对第二种癌症发生率的影响尚不清楚。我们报告了234例在一线治疗中接受基于氟达拉滨、环磷酰胺和利妥昔单抗(FCR)方案治疗的患者中第二种癌症的特征、发生率、结局及相关因素。第二种癌症的风险比一般人群的预期风险高2.38倍。93例患者(40%)在FCR治疗前患有其他癌症,66例患者(28%)在FCR治疗后患有其他癌症。治疗相关的急性髓系白血病/骨髓增生异常综合征(t-AML/MDS)(5.1%)和 Richter转化(RT)(9%)的发生率较高,而实体瘤并未增加。与有或无既往癌症的患者相比,一线FCR治疗后发生第二种癌症的患者总生存期较短(中位生存期为4.5年)。一线FCR治疗后第二种癌症的风险主要归因于t-AML/MDS和RT的高发生率,并且正如推测的那样,受影响患者的生存期较短。