Hématologie Biologique, Centre Hospitalier Universitaire de Limoges, Limoges, France.
Faculté de Médecine de Limoges, UMR CNRS 7276 CRIBL, Limoges, France.
Cancer Med. 2018 Jun;7(6):2621-2628. doi: 10.1002/cam4.1510. Epub 2018 May 9.
More than 35 years after the Binet classification, there is still a need for simple prognostic markers in chronic lymphocytic leukemia (CLL). Here, we studied the treatment-free survival (TFS) impact of normal serum protein electrophoresis (SPE) at diagnosis. One hundred twelve patients with CLL were analyzed. The main prognostic factors (Binet stage; lymphocytosis; IGHV mutation status; TP53, SF3B1, NOTCH1, and BIRC3 mutations; and cytogenetic abnormalities) were studied. The frequencies of IGHV mutation status, cytogenetic abnormalities, and TP53, SF3B1, NOTCH1, and BIRC3 mutations were not significantly different between normal and abnormal SPE. Normal SPE was associated with Binet stage A, nonprogressive disease for 6 months, lymphocytosis below 30 G/L, and the absence of the IGHV3-21 gene rearrangement which is associated with poor prognosis. The TFS of patients with normal SPE was significantly longer than that of patients with abnormal SPE (log-rank test: P = 0.0015, with 51% untreated patients at 5.6 years and a perfect plateau afterward vs. a median TFS at 2.64 years for abnormal SPE with no plateau). Multivariate analysis using two different Cox models and bootstrapping showed that normal SPE was an independent good prognostic marker for either Binet stage, lymphocytosis, or IGHV mutation status. TFS was further increased when both normal SPE and mutated IGHV were present (log-rank test: P = 0.008, median not reached, plateau at 5.6 years and 66% untreated patients). A comparison with other prognostic markers suggested that normal SPE could reflect slowly advancing CLL disease. Altogether, our results show that a combination of normal SPE and mutated IGHV genes defines a subgroup of patients with CLL who evolve very slowly and who might never need treatment.
在比内分类法问世 35 年多以后,慢性淋巴细胞白血病(CLL)仍然需要简单的预后标志物。在这里,我们研究了初诊时正常血清蛋白电泳(SPE)对无治疗生存(TFS)的影响。我们分析了 112 例 CLL 患者。研究了主要预后因素(Binet 分期;淋巴细胞增多;IGHV 突变状态;TP53、SF3B1、NOTCH1 和 BIRC3 突变;细胞遗传学异常)。IGHV 突变状态、细胞遗传学异常以及 TP53、SF3B1、NOTCH1 和 BIRC3 突变的频率在正常 SPE 和异常 SPE 之间没有显著差异。正常 SPE 与 Binet 分期 A、6 个月内无进展性疾病、淋巴细胞计数低于 30G/L 以及缺乏与预后不良相关的 IGHV3-21 基因重排有关。正常 SPE 患者的 TFS 明显长于异常 SPE 患者(对数秩检验:P=0.0015,5.6 年内 51%未治疗患者无进展,此后达到完美平台,而异常 SPE 的中位 TFS 为 2.64 年,无平台)。使用两种不同的 Cox 模型和自举法进行的多变量分析表明,正常 SPE 是 Binet 分期、淋巴细胞增多或 IGHV 突变状态的独立良好预后标志物。当正常 SPE 和突变 IGHV 同时存在时,TFS 进一步增加(对数秩检验:P=0.008,中位值未达到,5.6 年达到平台,66%未治疗患者)。与其他预后标志物的比较表明,正常 SPE 可反映进展缓慢的 CLL 疾病。总之,我们的结果表明,正常 SPE 和突变 IGHV 基因的组合定义了一组 CLL 患者,他们的病情进展非常缓慢,可能永远不需要治疗。