Arosio Giulia, Sharma Geeta G, Villa Matteo, Mauri Mario, Crespiatico Ilaria, Fontana Diletta, Manfroni Chiara, Mastini Cristina, Zappa Marina, Magistroni Vera, Ceccon Monica, Redaelli Sara, Massimino Luca, Garbin Anna, Lovisa Federica, Mussolin Lara, Piazza Rocco, Gambacorti-Passerini Carlo, Mologni Luca
Department Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.
Department Hematology & Hematopoietic Cell Transplantation, City of Hope National Medical Center, 1500 E Duarte Rd, Duarte, CA 91010, USA.
Cancers (Basel). 2021 Sep 1;13(17):4422. doi: 10.3390/cancers13174422.
Anaplastic lymphoma kinase-positive (ALK+) anaplastic large-cell lymphoma (ALCL) is a subtype of non-Hodgkin lymphoma characterized by expression of the oncogenic NPM/ALK fusion protein. When resistant or relapsed to front-line chemotherapy, ALK+ ALCL prognosis is very poor. In these patients, the ALK inhibitor crizotinib achieves high response rates, however 30-40% of them develop further resistance to crizotinib monotherapy, indicating that new therapeutic approaches are needed in this population. We here investigated the efficacy of upfront rational drug combinations to prevent the rise of resistant ALCL, in vitro and in vivo. Different combinations of crizotinib with CHOP chemotherapy, decitabine and trametinib, or with second-generation ALK inhibitors, were investigated. We found that in most cases combined treatments completely suppressed the emergence of resistant cells and were more effective than single drugs in the long-term control of lymphoma cells expansion, by inducing deeper inhibition of oncogenic signaling and higher rates of apoptosis. Combinations showed strong synergism in different ALK-dependent cell lines and better tumor growth inhibition in mice. We propose that drug combinations that include an ALK inhibitor should be considered for first-line treatments in ALK+ ALCL.
间变性淋巴瘤激酶阳性(ALK+)间变性大细胞淋巴瘤(ALCL)是非霍奇金淋巴瘤的一种亚型,其特征为致癌性NPM/ALK融合蛋白的表达。当对一线化疗耐药或复发时,ALK+ ALCL的预后非常差。在这些患者中,ALK抑制剂克唑替尼可实现较高的缓解率,然而其中30%-40%的患者会对克唑替尼单药治疗产生进一步耐药,这表明该人群需要新的治疗方法。我们在此研究了前期合理药物联合方案在体外和体内预防耐药性ALCL出现的疗效。研究了克唑替尼与CHOP化疗、地西他滨和曲美替尼的不同联合方案,或与第二代ALK抑制剂的联合方案。我们发现,在大多数情况下,联合治疗完全抑制了耐药细胞的出现,并且通过诱导对致癌信号的更深度抑制和更高的凋亡率,在长期控制淋巴瘤细胞增殖方面比单药更有效。联合方案在不同的ALK依赖细胞系中显示出强烈的协同作用,并且在小鼠中对肿瘤生长的抑制效果更好。我们建议,对于ALK+ ALCL的一线治疗,应考虑包含ALK抑制剂的药物联合方案。