John Theurer Cancer Center, Hackensack Meridian Health, Hackensack, NJ, 07601, USA.
Hackensack Meridian School of Medicine, Nutley, NJ, USA.
Curr Treat Options Oncol. 2021 Oct 25;22(12):111. doi: 10.1007/s11864-021-00909-1.
When selecting therapy for patients with indolent non-Hodgkin lymphoma (iNHL) including follicular (FL), marginal zone (MZL), small lymphocytic (SLL), and lymphoplasmacytic lymphoma (LPL)/Waldenström macroglobulinemia (WM), there are several factors to consider. With a median age around 70 at diagnosis, many patients have accumulated comorbid conditions that may limit treatment options. Although incurable for most, iNHL is a chronic disease with a median overall survival measured in years to decades. This long natural history changes the risk-to-benefit balance with a lower acceptance of toxicity early in the treatment course compared to that of aggressive lymphomas. Despite a recent rapid increase in available therapies, overall progress in iNHL has been slow for several reasons. Initial trials grouped iNHLs together making it challenging to appreciate the differential activity among subtypes. We have not been able to develop prognostic models that maintain validity in the era of chemotherapy-free options. Predictive markers have been elusive and without identified molecular signatures, it is challenging to select and sequence therapy. With these clinical factors in mind, in addition to the heterogeneity among and within iNHLs, I do not have a standard treatment algorithm and feel each patient should have an individualized treatment approach. This review focuses on recent updates and controversies in the management of iNHL with a focus on FL and MZL.
在为惰性非霍奇金淋巴瘤(iNHL)患者选择治疗方案时,包括滤泡性(FL)、边缘区(MZL)、小淋巴细胞(SLL)和淋巴浆细胞性淋巴瘤(LPL)/华氏巨球蛋白血症(WM),需要考虑几个因素。大多数患者在诊断时的中位年龄在 70 岁左右,有许多累积的合并症,这可能会限制治疗方案的选择。尽管大多数 iNHL 是不可治愈的,但它是一种慢性病,中位总生存期可测量为数年至数十年。这种长期的自然史改变了风险与获益的平衡,与侵袭性淋巴瘤相比,在治疗早期对毒性的接受程度较低。尽管最近可用的治疗方法迅速增加,但由于多种原因,iNHL 的总体进展一直缓慢。最初的试验将 iNHL 分组在一起,使得难以评估亚型之间的差异活性。我们还没有能够开发出在无化疗选择时代保持有效性的预后模型。预测标志物难以捉摸,并且在没有确定的分子特征的情况下,选择和测序治疗具有挑战性。考虑到这些临床因素,以及 iNHL 之间和内部的异质性,我没有标准的治疗算法,并且认为每个患者都应该有个体化的治疗方法。本综述重点介绍了 iNHL 治疗的最新进展和争议,重点是 FL 和 MZL。