Bobin Arthur, Gruchet Cécile, Guidez Stéphanie, Gardeney Hélène, Nsiala Makunza Laly, Vonfeld Mathilde, Lévy Anthony, Cailly Laura, Sabirou Florence, Systchenko Thomas, Moya Niels, Leleu Xavier
Department of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.
Cancers (Basel). 2021 Oct 18;13(20):5210. doi: 10.3390/cancers13205210.
Novel treatments are needed to address the lack of options for patients with relapsed or refractory multiple myeloma. Even though immunotherapy-based treatments have revolutionized the field in recent years, offering new opportunities for patients, there is still no curative therapy. Thus, non-immunologic agents, which have proven effective for decades, are still central to the treatment of multiple myeloma, especially for advanced disease. Building on their efficacy in myeloma, the development of proteasome inhibitors and immunomodulatory drugs has been pursued, and has led to the emergence of a novel generation of agents (e.g., carfilzomib, ixazomib, pomalidomide). The use of alkylating agents is decreasing in most treatment regimens, but melflufen, a peptide-conjugated alkylator with a completely new mechanism of action, offers interesting opportunities. Moreover, with the identification of novel targets, new drug classes have entered the myeloma armamentarium, such as XPO1 inhibitors (selinexor), HDAC inhibitors (panobinostat), and anti-BCL-2 agents (venetoclax). New pathways are still being explored, especially the possibility of a mutation-driven strategy, as biomarkers and targeted treatments are increasing. Though multiple myeloma is still considered incurable, the treatment options are expanding and are progressively becoming more diverse, largely because of the continuous development of non-immunologic agents.
需要新的治疗方法来解决复发或难治性多发性骨髓瘤患者治疗选择匮乏的问题。尽管近年来基于免疫疗法的治疗彻底改变了该领域,为患者带来了新的机遇,但仍然没有治愈性疗法。因此,数十年来已被证明有效的非免疫药物仍然是多发性骨髓瘤治疗的核心,尤其是对于晚期疾病。在其对骨髓瘤疗效的基础上,人们一直在研发蛋白酶体抑制剂和免疫调节药物,并催生了新一代药物(如卡非佐米、伊沙佐米、泊马度胺)。在大多数治疗方案中,烷化剂的使用正在减少,但美法仑氟芬,一种具有全新作用机制的肽缀合烷化剂,提供了有趣的机遇。此外,随着新靶点的确定,新的药物类别已进入骨髓瘤治疗药物库,如XPO1抑制剂(塞利尼索)、HDAC抑制剂(帕比司他)和抗BCL-2药物(维奈克拉)。新的途径仍在探索中,特别是突变驱动策略的可能性,因为生物标志物和靶向治疗正在增加。尽管多发性骨髓瘤仍被认为无法治愈,但治疗选择正在扩大且日益多样化,这在很大程度上归功于非免疫药物的不断发展。