研究概要
味觉障碍是癌症治疗中一种具有临床后果但仍缺乏标准化的毒性反应。
中文摘要
味觉障碍是癌症治疗中一种具有临床后果但仍缺乏标准化的毒性反应。在免疫治疗时代,味觉障碍对接受免疫检查点抑制剂、嵌合抗原受体(CAR)T细胞疗法和T细胞重定向双特异性抗体的患者日益重要,其中多发性骨髓瘤中靶向G蛋白偶联受体家族C第5组成员D(GPRC5D)的治疗代表了一个尤其具有启发性的高负担模型。我们进行了一项结构化的批判性叙述性综述,并附有证据图谱。检索了PubMed/MEDLINE自建库至2026年6月,并辅以Google Scholar中的引文追踪、ClinicalTrials.gov检索以及与肿瘤营养、口腔支持治疗和癌症相关味觉功能障碍相关的指南文件。检索概念涵盖癌症相关味觉障碍、免疫治疗相关口腔毒性、GPRC5D/talquetamab相关味觉障碍、肿瘤营养、口腔-肠道微生物组生物学、天然味觉调节剂和基于miraculin的干预措施。味觉障碍可降低食欲、食物享受感、膳食多样性和蛋白质能量摄入,从而导致体重减轻、营养不良风险、痛苦、社交退缩,严重时甚至导致治疗调整或中止。现有证据具有异质性:一般癌症治疗相关味觉障碍得到更广泛的观察性和干预性文献支持;免疫治疗相关味觉障碍的系统性特征描述较少;而GPRC5D/talquetamab相关味觉障碍则代表了临床上最明显、最具靶点特异性的免疫治疗相关表型。新出现的初步数据提示,干燥的神秘果或含神秘果蛋白的产品可能改善癌症相关味觉障碍中部分味觉感知和营养参数,但在免疫治疗相关味觉障碍中的直接证据尚未确立。因此,我们提出一个受声称规范约束的精准支持治疗框架,整合系统性味觉表型分型、早期营养风险评估、口腔健康评估、关注微生物组但仅用于产生假设的终点、个体化风味与质地调整、在选定患者中谨慎使用天然味觉调节剂,以及对以患者为中心结局的迭代监测。未来试验应检验针对味觉障碍的营养与味觉调节支持治疗干预能否在不损害免疫治疗安全性或疗效的前提下改善摄入量、生活质量和治疗持续性。
展开英文摘要原文
Dysgeusia is a clinically consequential, but still under-standardized, toxicity of cancer treatment. In the immunotherapy era, taste disturbances are increasingly relevant for patients receiving immune checkpoint inhibitors, chimeric antigen receptor (CAR) T-cell therapies and T-cell-redirecting bispecific antibodies, with G protein-coupled receptor family C group 5 member D (GPRC5D)-directed treatment in multiple myeloma representing a particularly instructive high-burden model. We performed a structured critical narrative review with evidence mapping. PubMed/MEDLINE was searched from database inception to June 2026, complemented by citation tracking in Google Scholar, ClinicalTrials.gov searches and guideline documents relevant to oncology nutrition, oral supportive care and cancer-related taste dysfunction. Search concepts covered cancer-related dysgeusia, immunotherapy-associated oral toxicity, GPRC5D/talquetamab-associated dysgeusia, oncology nutrition, oral-gut microbiome biology, natural taste modulators and miraculin-based interventions. Dysgeusia can reduce appetite, food enjoyment, dietary diversity and protein energy intake, thereby contributing to weight loss, malnutrition risk, distress, social withdrawal and, in severe cases, treatment modification or discontinuation. Available evidence is heterogeneous: general cancer-treatment-associated dysgeusia is supported by broader observational and interventional literature; immunotherapy-associated dysgeusia is less systematically characterized; and GPRC5D/talquetamab-associated dysgeusia represents the most clinically visible and target-specific immunotherapy-associated phenotype. Emerging pilot data suggest that dried miracle berry or miraculin-containing products may improve selected taste perception and nutritional parameters in cancer-related dysgeusia, but direct evidence in immunotherapy-associated dysgeusia is not yet established. We, therefore, propose a claim-disciplined precision supportive-care framework integrating systematic taste phenotyping, early nutritional risk assessment, oral health evaluation, microbiome-aware but hypothesis-generating endpoints, individualized flavor and texture adaptation, cautious use of natural taste modulators in selected patients and iterative monitoring of patient-centered outcomes. Future trials should test whether dysgeusia-focused nutritional and taste-modulating supportive care interventions can improve intake, quality of life and treatment persistence without compromising immunotherapy safety or efficacy.
论文信息
- 作者
- Fleischer A
- 单位
- Department of Internal Medicine II/Psychosomatics, University Hospital Würzburg, 97080 Würzburg, Germany.Germany
- 文献类型
- 综述
- 期刊
- Nutrients2026 Jul 22