László Tamás, Pinczés László Imre, Bátai Bence, Varga Luca, Timár Botond, Gulyás Anita, Tárkányi Ilona, Plander Márk, Nagy Zsolt, Rajnics Péter, Egyed Miklós, Molnár Zsuzsa, Rottek János, Masszi András, Tamáska Péter, Szász Róbert, Illés Árpád, Alpár Donát, Magyari Ferenc, Bödör Csaba
HCEMM-SE Molecular Oncohematology Research Group, Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
MTA-SE Lendület Molecular Oncohematology Research Group, Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
J Pathol. 2025 Aug;266(4-5):395-404. doi: 10.1002/path.6434. Epub 2025 May 15.
In recent years, targeted therapies have become the standard of care for refractory/relapsed mantle cell lymphoma (MCL). Although the mutational profile of MCL has been extensively studied, there is a lack of understanding of resistance mechanisms and genetic factors that impact the response to novel treatments. Since patients relapsing on targeted treatment experience poor clinical outcomes, understanding the genetic foundation of resistance mechanisms in MCL is essential. In this study, we aimed to scrutinize the copy number profile and clonal dynamics of double-resistant MCL patients treated sequentially with Bruton's tyrosine kinase inhibitor (BTKi) and venetoclax using low-coverage whole genome sequencing (lcWGS). Samples obtained after systemic therapy showed more copy number alterations (CNAs) (p = 0.039; Wilcoxon) compared to samples collected before treatment initiation. Patients showing early progression on BTKi demonstrated CNAs affecting cytobands encompassing the coding regions of NOTCH1, TRAF2, BIRC2, BIRC3, and ATM. A deletion in chromosome 9p21.3 was identified in two out of three venetoclax-resistant patients. For patient MCL2, progressing on ibrutinib but showing venetoclax resistance, a 9p21.3 deletion was found throughout the disease course, with acquired SMARCA4-del(19)(p13.3-q13.11) and DLC1-del(8)(p23.2-q11.1) observed at relapse, highlighting their role in disease progression and therapy resistance. Using lcWGS, an innovative genome-wide approach, this study revealed novel putative primary and acquired resistance mechanisms in BTKi and venetoclax double-resistant MCL patients. © 2025 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
近年来,靶向治疗已成为难治性/复发性套细胞淋巴瘤(MCL)的标准治疗方法。尽管对MCL的突变谱已进行了广泛研究,但对于影响新型治疗反应的耐药机制和遗传因素仍缺乏了解。由于接受靶向治疗后复发的患者临床结局较差,因此了解MCL耐药机制的遗传基础至关重要。在本研究中,我们旨在使用低覆盖度全基因组测序(lcWGS)仔细研究先后接受布鲁顿酪氨酸激酶抑制剂(BTKi)和维奈克拉治疗的双重耐药MCL患者的拷贝数谱和克隆动态。与治疗开始前采集的样本相比,全身治疗后获得的样本显示出更多的拷贝数改变(CNA)(p = 0.039;Wilcoxon检验)。在BTKi治疗早期进展的患者中,CNA影响了包含NOTCH1、TRAF2、BIRC2、BIRC3和ATM编码区的细胞带。在三分之二的维奈克拉耐药患者中发现了9号染色体p21.3缺失。对于患者MCL2,在依鲁替尼治疗中进展但显示对维奈克拉耐药,在整个疾病过程中均发现9p21.3缺失,在复发时观察到获得性SMARCA4缺失(19)(p13.3-q13.11)和DLC1缺失(8)(p23.2-q11.1),突出了它们在疾病进展和治疗耐药中的作用。本研究使用lcWGS这种创新的全基因组方法,揭示了BTKi和维奈克拉双重耐药MCL患者新的推定原发性和获得性耐药机制。© 2025作者。《病理学杂志》由约翰·威利父子有限公司代表大不列颠及爱尔兰病理学会出版。