• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

骨髓增生异常综合征患者临床试验入组率低:原因及潜在解决方案。

Low clinical trial accrual of patients with myelodysplastic syndromes: Causes and potential solutions.

机构信息

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.

出版信息

Cancer. 2018 Dec 15;124(24):4601-4609. doi: 10.1002/cncr.31769. Epub 2018 Oct 5.

DOI:10.1002/cncr.31769
PMID:30289970
Abstract

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.

摘要

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。

相似文献

1
Low clinical trial accrual of patients with myelodysplastic syndromes: Causes and potential solutions.骨髓增生异常综合征患者临床试验入组率低:原因及潜在解决方案。
Cancer. 2018 Dec 15;124(24):4601-4609. doi: 10.1002/cncr.31769. Epub 2018 Oct 5.
2
Connect MDS/AML: design of the myelodysplastic syndromes and acute myeloid leukemia disease registry, a prospective observational cohort study.连接骨髓增生异常综合征/急性髓系白血病:骨髓增生异常综合征和急性髓系白血病疾病登记处的设计,一项前瞻性观察队列研究。
BMC Cancer. 2016 Aug 19;16:652. doi: 10.1186/s12885-016-2710-6.
3
Eligibility for clinical trials is unsatisfactory for patients with myelodysplastic syndromes, even at a tertiary referral center.即使在三级转诊中心,骨髓增生异常综合征患者参加临床试验的资格也不尽如人意。
Leuk Res. 2021 Sep;108:106611. doi: 10.1016/j.leukres.2021.106611. Epub 2021 May 11.
4
Low participation rates and disparities in participation in interventional clinical trials for myelodysplastic syndromes.骨髓增生异常综合征介入临床试验参与率低且存在差异。
Cancer. 2020 Nov 1;126(21):4735-4743. doi: 10.1002/cncr.33105. Epub 2020 Aug 7.
5
The impact of anaemia, transfusion dependency, comorbidities and polypharmacy in elderly patients with low-risk myelodysplastic syndromes.老年低危骨髓增生异常综合征患者贫血、输血依赖、合并症和多种药物治疗的影响。
Med Oncol. 2018 Feb 8;35(3):33. doi: 10.1007/s12032-018-1094-7.
6
Myelodysplastic syndromes in the United States: an update for clinicians.美国的骨髓增生异常综合征:临床医生最新资讯
Ann Med. 2014 Aug;46(5):283-9. doi: 10.3109/07853890.2014.898863. Epub 2014 Apr 10.
7
Myelodysplastic syndromes: 2015 Update on diagnosis, risk-stratification and management.骨髓增生异常综合征:2015 年诊断、风险分层和治疗更新。
Am J Hematol. 2015 Sep;90(9):831-41. doi: 10.1002/ajh.24102.
8
Myelodysplastic syndromes: 2018 update on diagnosis, risk-stratification and management.骨髓增生异常综合征:2018 年诊断、风险分层和治疗更新。
Am J Hematol. 2018 Jan;93(1):129-147. doi: 10.1002/ajh.24930.
9
Survey of oncologists' perceptions of barriers to accrual of older patients with breast carcinoma to clinical trials.肿瘤学家对老年乳腺癌患者参与临床试验的入组障碍认知的调查。
Cancer. 2002 Sep 1;95(5):989-96. doi: 10.1002/cncr.10792.
10
Hematopoietic Cell Transplantation for Myelodysplastic Syndromes.骨髓增生异常综合征的造血细胞移植
J Oncol Pract. 2016 Sep;12(9):786-92. doi: 10.1200/JOP.2016.015214.

引用本文的文献

1
Reducing clinical trial eligibility barriers for patients with MDS: an icMDS position statement.降低骨髓增生异常综合征患者临床试验的入选障碍:一份国际骨髓增生异常综合征工作组立场声明
Blood. 2025 Mar 27;145(13):1369-1381. doi: 10.1182/blood.2023023717.
2
Advancing drug development in myelodysplastic syndromes.推动骨髓增生异常综合征的药物研发
Blood Adv. 2025 Mar 11;9(5):1095-1104. doi: 10.1182/bloodadvances.2024014865.
3
Treatment of myelodysplastic syndromes in the era of precision medicine and immunomodulatory drugs: a focus on higher-risk disease.
精准医学和免疫调节药物时代骨髓增生异常综合征的治疗:关注高危疾病。
J Hematol Oncol. 2022 Aug 31;15(1):124. doi: 10.1186/s13045-022-01346-9.
4
Historical expectations with DNA methyltransferase inhibitor monotherapy in MDS: when is combination therapy truly "promising"?在 MDS 中使用 DNA 甲基转移酶抑制剂单药治疗的历史预期:何时联合治疗才真正“有前景”?
Blood Adv. 2022 May 10;6(9):2854-2866. doi: 10.1182/bloodadvances.2021006357.
5
Emerging Therapies for the Myelodysplastic Syndromes.骨髓增生异常综合征的新兴疗法
Clin Hematol Int. 2019 Dec 6;2(1):13-17. doi: 10.2991/chi.d.191202.001. eCollection 2020 Mar.
6
Outcomes of patients with hematologic malignancies and COVID-19: a report from the ASH Research Collaborative Data Hub.血液系统恶性肿瘤合并 COVID-19 患者的结局:来自 ASH 研究协作数据中心的报告。
Blood Adv. 2020 Dec 8;4(23):5966-5975. doi: 10.1182/bloodadvances.2020003170.
7
Genomic Biomarkers to Predict Resistance to Hypomethylating Agents in Patients With Myelodysplastic Syndromes Using Artificial Intelligence.利用人工智能预测骨髓增生异常综合征患者对去甲基化药物耐药性的基因组生物标志物
JCO Precis Oncol. 2019;3. doi: 10.1200/po.19.00119. Epub 2019 Sep 20.
8
Representation of therapy-related myelodysplastic syndrome in clinical trials over the past 20 years.过去 20 年临床试验中治疗相关骨髓增生异常综合征的表现。
Blood Adv. 2019 Sep 24;3(18):2738-2747. doi: 10.1182/bloodadvances.2019000293.