Voorhies Benjamin N, Stephens Deborah M
Division of Hematology and Hematologic Malignancies, Department of Internal Medicine, University of Utah, Salt Lake City, UT, 84112, USA.
Huntsman Cancer Institute, University of Utah, 1950 Circle of Hope, Room 3364, Salt Lake City, UT, 84112, USA.
Curr Treat Options Oncol. 2017 Feb;18(2):12. doi: 10.1007/s11864-017-0450-8.
The front-line management of patients with chronic lymphocytic leukemia (CLL) has evolved significantly in recent years due to introduction of novel, targeted agents. Upon CLL diagnosis, physicians should determine whether treatment or careful observation is indicated. Once treatment is required, choice of therapy should be based on the age and fitness of the patient and the distinct molecular profile of their disease. As multiple novel agents are in various stages of development, all patients regardless of their age, fitness, and disease risk should be evaluated for clinical trial participation before initiating any front-line therapy. If no clinical trial is available, we provide our recommendations for front-line treatment of CLL patients. Healthy, young patients with low-risk disease (mutated IgVH, del (13q)) should be offered fludarabine, chlorambucil, and rituximab (FCR), while similar patients with high-risk disease (unmutated IgVH, del (17p), del (11q), and complex karyotype) should be considered for ibrutinib therapy. For those young, fit patients with high-risk disease and a contraindication to ibrutinib, FCR, or high-dose methylprednisolone and rituximab are options. In regard to older, unfit patients, a careful assessment of their fitness and ability to tolerate treatment should be undertaken before starting therapy. Those who have poor performance and multiple medical comorbidities should be considered for palliative care alone. However, those who are fit enough for treatment can be offered ibrutinib. If there is a contraindication to ibrutinib, they can be separated into low- and high-risk molecular groups. For the low-risk patients, bendamustine and rituximab or obinutuzumab and chlorambucil can be considered. For the high-risk patients, treatment with rituximab and lenalidomide is an option. Herein, we provide an evidence-based front-line treatment algorithm for CLL patients based upon fitness and molecular risk.
近年来,由于新型靶向药物的引入,慢性淋巴细胞白血病(CLL)患者的一线管理有了显著进展。在CLL诊断后,医生应确定是需要治疗还是进行密切观察。一旦需要治疗,治疗方案的选择应基于患者的年龄、身体状况以及疾病的独特分子特征。由于多种新型药物正处于不同的研发阶段,所有患者,无论其年龄、身体状况和疾病风险如何,在开始任何一线治疗前都应评估是否适合参加临床试验。如果没有可用的临床试验,我们提供CLL患者一线治疗的建议。健康的低风险疾病(IgVH突变、del(13q))年轻患者应接受氟达拉滨、苯丁酸氮芥和利妥昔单抗(FCR)治疗,而类似的高风险疾病(IgVH未突变、del(17p)、del(11q)和复杂核型)患者应考虑接受伊布替尼治疗。对于那些有高风险疾病且有伊布替尼禁忌证的年轻、身体状况良好的患者,FCR或大剂量甲泼尼龙和利妥昔单抗是选择方案。对于老年、身体状况不佳的患者,在开始治疗前应仔细评估其身体状况和耐受治疗的能力。那些表现不佳且有多种内科合并症的患者应仅考虑姑息治疗。然而,那些身体状况足以接受治疗的患者可以接受伊布替尼治疗。如果有伊布替尼禁忌证,可以将他们分为低风险和高风险分子组。对于低风险患者,可以考虑苯达莫司汀和利妥昔单抗或奥滨尤妥珠单抗和苯丁酸氮芥。对于高风险患者,利妥昔单抗和来那度胺治疗是一种选择。在此,我们基于身体状况和分子风险为CLL患者提供了一种循证一线治疗算法。