High-Dose Oral Vitamin D for Toxic Effects of the Skin Associated With Chemotherapy and Radiation.

IF 10.9 1区 医学 Q1 DERMATOLOGY
Mihir K Patil, Goranit Sakunchotpanit, Sushila A Toulmin, Natalie Braun, Sofia Milosavljevic, Farrah L Ezzeddine, Thomas Z Rohan, W Austin Wyant, Lauren M Guggina, Vinod E Nambudiri, Christopher Iriarte
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引用次数: 0

Abstract

Importance: Severe cutaneous toxic effects from chemotherapy and radiation often require treatment interruptions. High-dose oral vitamin D (hdVD) has shown potential as a rapid immunomodulator in experimental models and small human studies, but robust clinical data in oncology populations remain limited.

Objective: To evaluate the clinical response, safety profile, and time to improvement for hdVD in patients with toxic erythema of chemotherapy (TEC) and acute radiation dermatitis (ARD).

Design, setting, and participants: This retrospective multicenter case series included 33 patients treated across 3 academic medical centers between December 2021 and January 2024. Eligible participants were those receiving hdVD (100 000 international units) for TEC or ARD with at least 10 days of follow-up.

Exposures: One or 2 oral doses of 100 000 international units of cholecalciferol or ergocalciferol.

Main outcomes and measures: The primary outcomes were time to patient-reported symptomatic relief and clinician-assessed objective improvement in erythema (using a 5-point Likert scale). Secondary outcomes included changes in serum calcium and the ability to continue anticancer therapy.

Results: Among 33 patients (mean [SD] age, 60.9 [14.6] years; 19 [58%] female), 28 (85%) had TEC and 5 (15%) had ARD. Subjective symptom relief was reported by 26 of 30 patients (87%) within 10 days of treatment. The median (range) time to improvement was 5 (1-28) days overall and 3 (1-16) days for the inpatient subgroup. The mean (SD) Likert erythema score decreased from 4.36 (0.60) at baseline to 2.21 (1.36) by day 10. Patients with neutrophilic eccrine hidradenitis and Stevens-Johnson syndrome/toxic epidermal necrolysis-like subtypes showed the most rapid responses. No meaningful changes in serum calcium levels were observed, and 24 of the 33 patients (73%) continued anticancer therapy without interruption. No treatment-related adverse events were reported during the study.

Conclusions and relevance: In this case series, hdVD was associated with rapid symptomatic and objective improvement in chemotherapy- and radiation-induced toxic effects of the skin without treatment-related adverse events. These findings support further study of hdVD as a supportive care approach in oncodermatology.

大剂量口服维生素D对化疗和放疗相关皮肤的毒性作用。
重要性:化疗和放疗引起的严重皮肤毒性效应常常需要中断治疗。大剂量口服维生素D (hdVD)在实验模型和小型人体研究中显示出作为快速免疫调节剂的潜力,但在肿瘤人群中的可靠临床数据仍然有限。目的:评价hdVD治疗化疗毒性红斑(TEC)和急性放射性皮炎(ARD)患者的临床反应、安全性和改善时间。设计、环境和参与者:该回顾性多中心病例系列包括在2021年12月至2024年1月期间在3个学术医疗中心接受治疗的33名患者。符合条件的参与者是接受hdVD(100,000 000国际单位)治疗TEC或ARD的患者,随访时间至少为10天。暴露:一次或两次口服100,000 000国际单位的胆钙化醇或麦角钙化醇。主要结局和措施:主要结局是患者报告的症状缓解时间和临床评估的红斑客观改善(使用5点李克特量表)。次要结果包括血清钙的变化和继续抗癌治疗的能力。结果:33例患者(平均[SD]年龄60.9[14.6]岁,女性19例[58%]),28例(85%)发生TEC, 5例(15%)发生ARD。30例患者中有26例(87%)在治疗10天内主观症状缓解。总体改善的中位时间(范围)为5(1-28)天,住院亚组为3(1-16)天。平均(SD)李克特红斑评分从基线时的4.36(0.60)下降到第10天的2.21(1.36)。中性粒细胞外分泌汗腺炎和Stevens-Johnson综合征/中毒性表皮坏死松解样亚型患者反应最快。血清钙水平未见明显变化,33例患者中有24例(73%)持续接受抗癌治疗。研究期间未报告与治疗相关的不良事件。结论和相关性:在本病例系列中,hdVD与化疗和放疗引起的皮肤毒性作用的快速症状和客观改善有关,无治疗相关的不良事件。这些发现支持进一步研究hdVD作为肿瘤皮肤科的支持治疗方法。
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来源期刊
JAMA dermatology
JAMA dermatology DERMATOLOGY-
CiteScore
14.10
自引率
5.50%
发文量
300
期刊介绍: JAMA Dermatology is an international peer-reviewed journal that has been in continuous publication since 1882. It began publication by the American Medical Association in 1920 as Archives of Dermatology and Syphilology. The journal publishes material that helps in the development and testing of the effectiveness of diagnosis and treatment in medical and surgical dermatology, pediatric and geriatric dermatology, and oncologic and aesthetic dermatologic surgery. JAMA Dermatology is a member of the JAMA Network, a consortium of peer-reviewed, general medical and specialty publications. It is published online weekly, every Wednesday, and in 12 print/online issues a year. The mission of the journal is to elevate the art and science of health and diseases of skin, hair, nails, and mucous membranes, and their treatment, with the aim of enabling dermatologists to deliver evidence-based, high-value medical and surgical dermatologic care. The journal publishes a broad range of innovative studies and trials that shift research and clinical practice paradigms, expand the understanding of the burden of dermatologic diseases and key outcomes, improve the practice of dermatology, and ensure equitable care to all patients. It also features research and opinion examining ethical, moral, socioeconomic, educational, and political issues relevant to dermatologists, aiming to enable ongoing improvement to the workforce, scope of practice, and the training of future dermatologists. JAMA Dermatology aims to be a leader in developing initiatives to improve diversity, equity, and inclusion within the specialty and within dermatology medical publishing.
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