化疗诱导的周围神经病变研究:美国国立卫生研究院(NIH)拨款组合分析(2014-2023)。

IF 3.4 Q2 ONCOLOGY
Rachel D Altshuler, Lori M Minasian, Catherine A Schweppe, Nina S Kadan-Lottick
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引用次数: 0

摘要

背景:化疗引起的周围神经病变(CIPN)是癌症患者急性和长期毒性疾病。我们试图描述由美国国立卫生研究院(NIH)资助的CIPN研究的前景,并确定差距和机会。方法:使用NIH查询视图报告系统,我们确定了2014-2023年间180个竞争性拨款,其中包含摘要或具体目标中与CIPN相关的文本。这些被分类为临床前、临床或两者兼而有之,并通过临床前模型、临床人群、CIPN评估和/或临床试验设计来描述。我们通过与CIPN相关的NCORP网络确定了另外5个nci资助的试验。结果:185项研究中,125项为临床前研究,56项为临床研究,4项为临床前/临床研究。在临床前研究中,大多数研究采用啮齿类CIPN模型,其中17%为荷瘤模型。大多数临床前研究调查了紫杉醇;没有人研究新的免疫疗法。这60项临床研究53%为观察性研究,47%为介入性研究,主要集中在乳腺癌、未明确的癌症和结直肠癌的诊断上。结论:自2014年以来,NIH授予的CIPN拨款数量代表了一笔可观的投资,但仍然存在关键的差距和机会。临床前,模仿人类CIPN的新策略可能会提高可翻译性。cipn相关癌症诊断和治疗暴露的重要空白,包括新型药物,将受益于未来的研究。此外,需要对潜在长期CIPN的年轻患者进行临床研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chemotherapy-induced peripheral neuropathy research: a National Institutes of Health (NIH) grant portfolio analysis (2014-2023).

Background: Chemotherapy-induced peripheral neuropathy (CIPN) is a debilitating acute and long-term toxicity in cancer patients. We sought to describe the landscape of CIPN research funded by the National Institutes of Health (NIH) and identify gaps and opportunities.

Methods: Using the NIH Query View Report system, we identified 180 competitive grants between 2014-2023 containing text pertaining to CIPN in the Abstract or Specific Aims. These were categorized as preclinical, clinical, or both and described by preclinical model, clinical population, CIPN assessments, and/or clinical trial design. We identified 5 additional NCI-funded trials through the NCORP network pertaining to CIPN.

Results: Of 185 studies, 125 were preclinical, 56 clinical, and 4 both preclinical/clinical. Among pre-clinical studies, most studies utilized rodent CIPN models, of which 17% were tumor-bearing. Most preclinical studies investigated paclitaxel; none studied newer immune therapies. The 60 clinical studies were 53% observational and 47% interventional, focusing most frequently on breast cancer, unspecified cancers, and colorectal cancer diagnoses. Overall, 8% included patients <18 years, while a higher proportion included those 18-39 (85%), 40-64 (90%), and ≥65 (92%). Among 28 interventional trials, studies investigated behavioral interventions (39%), pharmacological agents (32%), and devices (29%).

Conclusions: The number of CIPN grants awarded by NIH since 2014 represent a substantial investment, but critical gaps and opportunities remain. Preclinically, novel strategies to mimic human CIPN may improve translatability. Important gaps in CIPN-associated cancer diagnoses and therapy exposures, including novel agents, would benefit from future research. Also, clinical studies are needed in young patients with potential long-term CIPN.

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来源期刊
JNCI Cancer Spectrum
JNCI Cancer Spectrum Medicine-Oncology
CiteScore
7.70
自引率
0.00%
发文量
80
审稿时长
18 weeks
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