Quality of life, neurocognitive functioning, psychological issues, sexuality and comorbidity more than 2 years after commencing immune checkpoint inhibitor treatment.

IF 10.3 1区 医学 Q1 IMMUNOLOGY
Wellington Candido, Annemarie Cecile Eggen, Mathilde Jalving, Ingeborg Bosma, Reinate D Horinga, Kelly C van Heuvelen, T Jeroen N Hiltermann, Sjoukje Oosting, Emoke Racz, Melanie M van der Klauw, Anna K L Reyners, Janine Nuver
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引用次数: 0

Abstract

Background: Increasing numbers of patients diagnosed with advanced cancer survive long-term after treatment with immune checkpoint inhibitors (ICIs). To design adequate interventions for these survivors, knowledge regarding quality of life (QOL) and its association with long-term and late effects of ICI treatment is required. Therefore, this study aimed to evaluate QOL, neurocognitive function, psychological issues, sexuality, and comorbidities in patients surviving at least 2 years after commencing ICI treatment.

Methods: We performed a cross-sectional study in patients with stage III-IV melanoma, non-small cell lung cancer (NSCLC), urothelial cell carcinoma (UCC), or renal cell carcinoma (RCC) who survived at least 2 years after the start of ICIs. We assessed QOL, neurocognitive function, psychological issues, sexual function and comorbidity in survivors. Additionally, we evaluated QOL of informal caregivers.

Results: 132 survivors (70 melanoma, 50 NSCLC, 12 UCC or RCC) and 80 caregivers were included. Median age was 65 years (range 30-85) and 50 survivors were women (38%). Median time since start and cessation of ICI treatment was 33 (range 21-91) and 18 (range 0-68) months, respectively. Average survivor QOL was comparable to the reference population, but 37 (28%) survivors had poor QOL. Depression and anxiety were negatively correlated with all QOL domains. Although immune-related adverse events were common, there was no association with lower QOL. Caregiver and survivor QOL were only weakly related. Neurocognitive concerns and formally tested neurocognitive impairment were present in 22 (17%) and 13 (15%) survivors, respectively, and were not associated with a diagnosis of brain metastases. Men had a high prevalence of erectile dysfunction and low sexual satisfaction. Half of the survivors met the criteria for the metabolic syndrome.

Conclusions: At least 2 years after the start of ICI treatment, one-quarter of cancer survivors had a clinically relevant lower QOL. This was associated with symptoms of depression and anxiety, but not with immune-related adverse events. Sexual issues and metabolic syndrome are prevalent. Survivorship care should address these issues in this population.

开始免疫检查点抑制剂治疗2年后的生活质量、神经认知功能、心理问题、性行为和合并症。
背景:越来越多的晚期癌症患者在接受免疫检查点抑制剂(ICIs)治疗后长期存活。为了为这些幸存者设计适当的干预措施,需要了解生活质量(QOL)及其与ICI治疗的长期和晚期影响的关系。因此,本研究旨在评估开始ICI治疗后存活至少2年的患者的生活质量、神经认知功能、心理问题、性行为和合并症。方法:我们对III-IV期黑色素瘤、非小细胞肺癌(NSCLC)、尿路上皮细胞癌(UCC)或肾细胞癌(RCC)患者进行了横断面研究,这些患者在ICIs开始后存活至少2年。我们评估了幸存者的生活质量、神经认知功能、心理问题、性功能和合并症。此外,我们评估了非正式照顾者的生活质量。结果:包括132名幸存者(70名黑色素瘤,50名非小细胞肺癌,12名UCC或RCC)和80名护理人员。中位年龄为65岁(30-85岁),50名幸存者为女性(38%)。ICI治疗开始和停止的中位时间分别为33个月(范围21-91)和18个月(范围0-68)。幸存者的平均生活质量与参考人群相当,但37名(28%)幸存者生活质量较差。抑郁、焦虑与生活质量各域呈负相关。虽然免疫相关的不良事件很常见,但与较低的生活质量没有关联。照顾者与生存者生活质量仅呈弱相关。分别有22名(17%)和13名(15%)幸存者存在神经认知问题和正式测试的神经认知障碍,并且与脑转移的诊断无关。男性勃起功能障碍患病率高,性满意度低。一半的幸存者符合代谢综合征的标准。结论:在开始ICI治疗至少2年后,1 / 4的癌症幸存者有临床相关的较低的生活质量。这与抑郁和焦虑症状有关,但与免疫相关的不良事件无关。性问题和代谢综合症很普遍。在这一人群中,生存护理应该解决这些问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal for Immunotherapy of Cancer
Journal for Immunotherapy of Cancer Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
17.70
自引率
4.60%
发文量
522
审稿时长
18 weeks
期刊介绍: The Journal for ImmunoTherapy of Cancer (JITC) is a peer-reviewed publication that promotes scientific exchange and deepens knowledge in the constantly evolving fields of tumor immunology and cancer immunotherapy. With an open access format, JITC encourages widespread access to its findings. The journal covers a wide range of topics, spanning from basic science to translational and clinical research. Key areas of interest include tumor-host interactions, the intricate tumor microenvironment, animal models, the identification of predictive and prognostic immune biomarkers, groundbreaking pharmaceutical and cellular therapies, innovative vaccines, combination immune-based treatments, and the study of immune-related toxicity.
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