Division of Hematological Malignancies, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Division of Hematology and Medical Oncology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Cancer. 2018 Dec 15;124(24):4601-4609. doi: 10.1002/cncr.31769. Epub 2018 Oct 5.
Despite few effective therapies, only a small percentage of patients diagnosed with myelodysplastic syndromes (MDS) in the United States are enrolled in prospective, interventional clinical trials. MDS-specific barriers to trial accrual include a high frequency of elderly patients with comorbid conditions, atypical disease features and uncertainty regarding the diagnosis (because other nonclonal processes also can cause dysplasia and cytopenias), a history of another nonmyeloid neoplasm resulting in therapy-related MDS, rapid disease recurrence after allogeneic stem cell transplantation, and an arbitrary division between MDS and acute myeloid leukemia. In addition, barriers to accrual that are common to other oncology populations, such as difficulty traveling to clinical trial enrollment sites and narrow trial eligibility criteria, also prevent patients with MDS from enrolling in studies. Collectively these barriers must be assessed systematically, and creative solutions are needed to improve outcomes for this needy patient population.
尽管有几种有效的疗法,但在美国被诊断为骨髓增生异常综合征 (MDS) 的患者中,只有一小部分被纳入前瞻性干预性临床试验。影响患者入组临床试验的因素包括高龄患者合并症较多、疾病特征不典型以及对诊断的不确定(因为其他非克隆性过程也可能导致发育不良和细胞减少)、既往非髓性恶性肿瘤导致治疗相关 MDS、异基因造血干细胞移植后疾病快速复发以及 MDS 和急性髓细胞白血病之间的任意划分。此外,其他肿瘤患者中常见的入组障碍,如难以前往临床试验入组点和较窄的试验纳入标准,也阻碍了 MDS 患者参加研究。总之,这些障碍必须系统地评估,并需要创造性的解决方案来改善这一需要帮助的患者群体的预后。