Morilla Alison, Gonzalez de Castro David, Del Giudice Ilaria, Osuji Nnenna, Else Monica, Morilla Ricardo, Brito Babapulle Vasantha, Rudenko Hannah, Matutes Estella, Dearden Claire, Catovsky Daniel, Morgan Gareth J
Section of Haemato-Oncology, The Institute of Cancer Research, Sutton, Surrey, UK.
Leuk Lymphoma. 2008 Nov;49(11):2108-15. doi: 10.1080/10428190802360810.
ZAP-70, CD38 and IGHV mutations have all been reported to have prognostic impact in chronic lymphocytic leukemia (CLL), both individually and in paired combinations. We aimed to determine whether the combination of all three factors provided more refined prognostic information concerning the treatment-free interval (TFI) from diagnosis. ZAP-70, CD38 and IGHV mutations were evaluated in 142 patients. Combining all three factors, the ZAP-70-/CD38-/Mutated group showed the longest median TFI (62 months, n = 37), ZAP-70+/CD38+/Unmutated cases the shortest (11 months, n = 37) and cases discordant for > or = 1 factor, an intermediate TFI (27 months, n = 68) (p = 0.006). Analysis of discordant cases revealed values that were otherwise masked when measuring single prognostic factors. The presence or absence of cytogenetic abnormalities did not explain the variability among discordant cases. Simultaneous analysis of ZAP-70, CD38 and IGHV mutations in CLL provides more discriminatory prediction of TFI than any factor alone.
据报道,ZAP-70、CD38和IGHV突变在慢性淋巴细胞白血病(CLL)中均具有预后影响,无论是单独还是成对组合。我们旨在确定这三个因素的组合是否能提供有关从诊断开始的无治疗间隔(TFI)的更精确的预后信息。对142例患者的ZAP-70、CD38和IGHV突变进行了评估。综合考虑这三个因素,ZAP-70阴性/CD38阴性/突变组的中位TFI最长(62个月,n = 37),ZAP-70阳性/CD38阳性/未突变病例最短(11个月,n = 37),而在≥1个因素上不一致的病例,TFI处于中间水平(27个月,n = 68)(p = 0.006)。对不一致病例的分析揭示了在测量单一预后因素时被掩盖的值。细胞遗传学异常的存在与否并不能解释不一致病例之间的变异性。对CLL患者同时进行ZAP-70、CD38和IGHV突变分析,比单独任何一个因素都能更具区分性地预测TFI。