Strategic Research Program on CLL, IRCCS Ospedale San Raffaele.
Università Vita-Salute San Raffaele, Milan, Italy.
Curr Opin Oncol. 2019 Nov;31(6):568-573. doi: 10.1097/CCO.0000000000000585.
This review provides guidance in the rapidly changing scenario of chronic lymphocytic leukemia (CLL) treatment. New studies as well as updates of other seminal ones have been recently presented and are likely to change the management of patients with CLL in everyday clinical practice.
Kinase inhibitors (e.g. ibrutinib and idelalisib) have transformed the treatment paradigm in CLL in both front-line and relapsed/refractory patients. Longer follow-up data are now available supporting the safety of ibrutinib and the continuous administration required per current label. Novel studies show the superiority of the drug alone or in combination with monoclonal antibodies compared with standard chemoimmunotherapy. The combination of venetoclax and obinutuzumab (treatment-naïve, only in United States) or rituximab (relapsed/refractory) has granted approval from the regulatory authorities in United States and Europe, based on phase 3 randomized studies. These novel chemo-free combinations allow for fixed-duration treatment and undetectable minimal residual disease. Novel targeted strategies including second and third generation BTK and PI3K inhibitors are currently under investigation and promise to further improve the CLL treatment armamentarium. The chimeric-antigen receptor (CAR) T cells are coming to the stage with promising efficacy and new challenges.
A bright chemo-free era for CLL patients is just around the corner. A deep knowledge of currently available evidences is key to tailor treatment choice and optimize long-term tolerability and disease control. Fixed-duration combinations are investigated to allow treatment holidays and avoid the emergence of resistant clones under the selective pressure of continuous treatment.
本综述旨在为慢性淋巴细胞白血病(CLL)治疗的快速变化提供指导。最近提出了新的研究结果以及其他重要研究的更新结果,这些结果可能会改变 CLL 患者在日常临床实践中的治疗管理。
激酶抑制剂(例如伊布替尼和idelalisib)改变了 CLL 患者的一线和复发/难治性患者的治疗模式。目前,更长的随访数据支持伊布替尼的安全性和当前标签要求的持续给药。新的研究表明,与标准化疗免疫疗法相比,该药物单独或联合使用单克隆抗体具有优越性。venetoclax 和 obinutuzumab(初治,仅在美国)或利妥昔单抗(复发/难治)的联合治疗已基于 3 期随机研究获得美国和欧洲监管机构的批准。这些新型无化疗联合治疗可实现固定疗程治疗和不可检测的微小残留疾病。目前正在研究新的靶向策略,包括第二代和第三代 BTK 和 PI3K 抑制剂,有望进一步改善 CLL 的治疗方法。嵌合抗原受体(CAR)T 细胞正在崭露头角,具有令人鼓舞的疗效和新的挑战。
CLL 患者的无化疗光明时代即将到来。深入了解当前可用的证据是制定治疗选择和优化长期耐受性和疾病控制的关键。正在研究固定疗程的联合治疗,以允许治疗假期,并避免在连续治疗的选择性压力下出现耐药克隆。