Chemotherapy-induced peripheral neuropathy research: a National Institutes of Health (NIH) grant portfolio analysis (2014-2023)

医学 临床试验 化疗所致周围神经病变 乳腺癌 临床研究设计 肿瘤科 人口 周围神经病变 癌症 观察研究 内科学 临床研究 糖尿病 内分泌学 环境卫生
作者
Rachel D. Altshuler,Lori M. Minasian,Catherine A. Schweppe,Nina S. Kadan‐Lottick
出处
期刊:JNCI Cancer Spectrum [Oxford University Press]
被引量:2
标识
DOI:10.1093/jncics/pkaf039
摘要

Abstract 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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