Forero-Castro Maribel, Robledo Cristina, Lumbreras Eva, Benito Rocio, Hernández-Sánchez Jesús M, Hernández-Sánchez María, García Juan L, Corchete-Sánchez Luis A, Tormo Mar, Barba Pere, Menárguez Javier, Ribera Jordi, Grande Carlos, Escoda Lourdes, Olivier Carmen, Carrillo Estrella, García de Coca Alfonso, Ribera Josep-María, Hernández-Rivas Jesús M
Cancer Research Centre, IBSAL, IBMCC, University of Salamanca, CSIC, Salamanca, Spain.
School of Biological Sciences (GEBIMOL), Pedagogical and Technological University of Colombia (UPTC), Colombia, IN, USA.
Br J Haematol. 2016 Feb;172(3):428-38. doi: 10.1111/bjh.13849. Epub 2015 Nov 16.
The introduction of Rituximab has improved the outcome and survival rates of Burkitt lymphoma (BL). However, early relapse and refractoriness are current limitations of BL treatment and new biological factors affecting the outcome of these patients have not been explored. This study aimed to identify the presence of genomic changes that could predict the response to new therapies in BL. Forty adolescent and adult BL patients treated with the Dose-Intensive Chemotherapy Including Rituximab (Burkimab) protocol (Spanish Programme for the Study and Treatment of Haematological Malignancies; PETHEMA) were analysed using array-based comparative genomic hybridization (CGH). In addition, the presence of TP53, TCF3 (E2A), ID3 and GNA13 mutations was assessed by next-generation sequencing (NGS). Ninety-seven per cent of the patients harboured genomic imbalances. Losses on 11q, 13q, 15q or 17p were associated with a poor response to Burkimab therapy (P = 0·038), shorter progression-free survival (PFS; P = 0·007) and overall survival (OS; P = 0·009). The integrative analysis of array-CGH and NGS showed that 26·3% (5/19) and 36·8% (7/19) of patients carried alterations in the TP53 and TCF3 genes, respectively. TP53 alterations were associated with shorter PFS (P = 0·011) while TCF3 alterations were associated with shorter OS (P = 0·032). Genetic studies could be used for risk stratification of BL patients treated with the Burkimab protocol.
利妥昔单抗的引入改善了伯基特淋巴瘤(BL)的治疗效果和生存率。然而,早期复发和难治性是目前BL治疗的局限性,尚未探索影响这些患者治疗效果的新生物因素。本研究旨在确定可能预测BL对新疗法反应的基因组变化的存在情况。使用基于芯片的比较基因组杂交(CGH)分析了40例接受包括利妥昔单抗的剂量密集化疗方案(Burkimab方案,西班牙血液系统恶性肿瘤研究与治疗项目;PETHEMA)治疗的青少年和成年BL患者。此外,通过下一代测序(NGS)评估了TP53、TCF3(E2A)、ID3和GNA13基因突变的存在情况。97%的患者存在基因组失衡。11q、13q、15q或17p缺失与对Burkimab治疗反应不佳(P = 0·038)、无进展生存期(PFS)较短(P = 0·007)和总生存期(OS)较短(P = 0·009)相关。阵列CGH和NGS的综合分析显示,分别有26·3%(5/19)和36·8%(7/19)的患者TP53和TCF3基因发生改变。TP53改变与较短的PFS相关(P = 0·011),而TCF3改变与较短的OS相关(P = 0·032)。基因研究可用于对接受Burkimab方案治疗的BL患者进行风险分层。