Department of Medicine, Hematology/Oncology, WIlmot Cancer Institute, University of Rochester Medical Center, Rochester, New York.
Department of Lymphoma/Myeloma, MD Anderson Cancer Center, Houston.
Ann Oncol. 2017 Sep 1;28(9):2094-2106. doi: 10.1093/annonc/mdx189.
For the majority of patients with newly diagnosed follicular lymphoma (FL), current treatments, while not curative, allow for long remission durations. However, several important needs remain unaddressed. Studies have consistently shown that ∼20% of patients with FL experience disease progression within 2 years of first-line treatment, and consequently have a 50% risk of death in 5 years. Better characterization of this group of patients at diagnosis may provide insight into those in need of alternate or intensive therapies, facilitate a precision approach to inform clinical trials, and allow for improved patient counseling. Prognostic methods to date have employed clinical parameters, genomic methods, and a wide assortment of biological and biochemical markers, but none so far has been able to adequately identify this high-risk population. Advances in the first-line treatment of FL with chemoimmunotherapy have led to a median progression-free survival (PFS) of approximately 7 years; creating a challenge in the development of clinical trials where PFS is a primary end point. A surrogate end point that accurately predicts PFS would allow for new treatments to reach patients with FL sooner, or lessen toxicity, time, and expense to those patients requiring little to no therapy. Quality of response to treatment may predict PFS and overall survival in FL; as such complete response rates, either alone or in conjunction with PET imaging or minimal residual disease negativity, are being studied as surrogates, with complete response at 30 months after induction providing the strongest surrogacy evidence to date. A better understanding of how to optimize quality of life in the context of this chronic illness is another important focus deserving of further study. Ongoing efforts to address these important unmet needs are herein discussed.
对于大多数新诊断的滤泡性淋巴瘤 (FL) 患者,目前的治疗方法虽然不能治愈,但可以延长缓解期。然而,仍有几个重要的需求尚未得到满足。研究表明,约 20%的 FL 患者在一线治疗后 2 年内出现疾病进展,因此在 5 年内有 50%的死亡风险。在诊断时更好地描述这组患者,可能有助于发现需要替代或强化治疗的患者,为临床试验提供信息,并改善患者咨询。迄今为止,预后方法采用了临床参数、基因组方法以及各种生物和生化标志物,但没有一种方法能够充分识别这一高危人群。一线化疗免疫治疗 FL 的进展,使无进展生存期(PFS)中位数达到约 7 年;这给以 PFS 为主要终点的临床试验的发展带来了挑战。一个能够准确预测 PFS 的替代终点,将使新的治疗方法更快地惠及 FL 患者,或减轻那些几乎不需要治疗的患者的毒性、时间和费用。对治疗的反应质量可能预测 FL 的 PFS 和总生存期;因此,完全缓解率(无论是单独使用还是结合 PET 成像或微小残留疾病阴性率)正在作为替代终点进行研究,诱导后 30 个月的完全缓解提供了迄今为止最强的替代证据。更好地了解如何在这种慢性病的背景下优化生活质量是另一个值得进一步研究的重要焦点。正在努力解决这些重要的未满足需求。