Characterization of Hospital Admissions During Immune Checkpoint Inhibitor Therapy: Insights From the ICOG Study

IF 3.1 2区 医学 Q2 ONCOLOGY Cancer Medicine Pub Date : 2025-01-25 DOI:10.1002/cam4.70582
Jonas Paul Wiegmann, Tabea Fröhlich, Nora Möhn, Laura Duzzi, Emily Narten, Johanna Aurich, Janin Thomas, Lea Grote-Levi, Susann Mahjoub, Dominik Berliner, Thomas Wirth, Heiko Golpon, Benjamin-Alexander Bollmann, Imke Von Wasilewski, Ralf Gutzmer, Florian H. Heidel, Thomas Skripuletz, Gernot Beutel, Philipp Ivanyi, ICOG-CCCH (Immune Cooperative Oncology Group, Comprehensive Cancer Center Hannover)
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Abstract

Introduction

Immune checkpoint inhibitors (ICI) have improved the therapeutic arsenal in outpatient oncology care; however, data on necessity of hospitalizations associated with immune-related adverse events (irAEs) are scarce. Here, we characterized hospitalizations of patients undergoing ICI, from the prospective cohort study of the immune cooperative oncology group (ICOG) Hannover.

Methods

Between 12/2019 and 06/2022, 237 patients were included. Clinical data and characteristics of ICI were collected during a 6-month observation period after the initiation of therapy. Descriptive statistics and Kaplan–Meier statistics were administered.

Results

During the observation period, 30/237 patients were hospitalized (HA(+)). Most common underlying tumor entities were malignant melanoma (59.5%), renal cell carcinoma (13.1%), and nonsmall-cell lung carcinoma (12.7%). HA(+) patients exhibited an increased rate of pulmonary and cerebral metastases. We observed a significantly higher hospitalization rate during dual ICI with Nivolumab and Ipilimumab (p = 0.001). The predominant irAEs for hospitalization were colitis (26.7%), followed by hypophysitis (13.3%), leading to a median hospitalization of 7 (1–34) days. Interdisciplinary consultations were frequent, especially to gastroenterology (46.7%) and neurology (26.7%). Although a trend toward a prolonged overall survival in the HA(+) subgroup was identified, no statistically significant differences were found.

Discussion

The hospitalization rate of 12.6% is comparable to rates reported in previous studies. There was a disproportionate admission of patients with immune-related colitis and hypophysitis compared to the prevalence described under ICI. We observed a high need for interdisciplinary consultations in line with the heterogeneity of immune-mediated side effects. Compared to non-hospitalized patients, there was no survival disadvantage in the HA(+) cohort.

Conclusion

With a relatively low hospitalization rate, short length of stay, and good clinical outcome, our data support the outpatient nature of ICI. The findings underscore the importance of interdisciplinary collaboration and vigilant monitoring of irAEs to ensure timely recognition and management.

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免疫检查点抑制剂治疗期间入院情况的特征:ICOG研究的启示
免疫检查点抑制剂(ICI)改善了门诊肿瘤护理的治疗武器库;然而,与免疫相关不良事件(irAEs)相关的住院必要性的数据很少。在这里,我们从汉诺威免疫肿瘤合作组(ICOG)的前瞻性队列研究中描述了接受ICI患者的住院情况。方法:2019年12月至2022年6月,纳入237例患者。在治疗开始后6个月的观察期内收集ICI的临床资料和特征。采用描述性统计和Kaplan-Meier统计。结果:观察期内30/237例患者住院(HA(+))。最常见的潜在肿瘤实体是恶性黑色素瘤(59.5%)、肾细胞癌(13.1%)和非小细胞肺癌(12.7%)。HA(+)患者表现出更高的肺和脑转移率。我们观察到尼武单抗和伊匹单抗双重ICI的住院率明显更高(p = 0.001)。导致住院的主要原因是结肠炎(26.7%),其次是垂体炎(13.3%),平均住院时间为7(1-34)天。跨学科会诊频繁,尤其是胃肠病学(46.7%)和神经病学(26.7%)。虽然HA(+)亚组有延长总生存期的趋势,但没有发现统计学上的显著差异。讨论:12.6%的住院率与以往研究报告的住院率相当。与ICI描述的患病率相比,免疫相关性结肠炎和垂体炎患者的入院比例不成比例。我们观察到,由于免疫介导的副作用的异质性,对跨学科咨询的需求很高。与非住院患者相比,HA(+)队列中没有生存劣势。结论:ICI的住院率较低,住院时间短,临床效果好,我们的数据支持其门诊性质。这一发现强调了跨学科合作和警惕地监测环境影响评估的重要性,以确保及时发现和管理。
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来源期刊
Cancer Medicine
Cancer Medicine ONCOLOGY-
CiteScore
5.50
自引率
2.50%
发文量
907
审稿时长
19 weeks
期刊介绍: Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas: Clinical Cancer Research Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations Cancer Biology: Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery. Cancer Prevention: Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach. Bioinformatics: Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers. Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.
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