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SUN-127 Diagnostic Challenges Associated with the Rising Incidence of Endocrine Toxicity in the Era of Combination Immunotherapy

机译:Sun-127结合免疫疗法时代内分泌毒性发病率上升相关的诊断挑战

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摘要

Background: Immune checkpoint blockade is now established as standard of care in several malignancies. Trials involving combined cytotoxic T lymphocyte associated protein 4 (CTLA4) and programmed cell death protein 1 (PD1) blockade demonstrate improved tumour responses in melanoma but at the cost of severe grade 3-4 immune related adverse events (irAEs) in 55%, and endocrine irAEs in up to 10% [1]. Immune-mediated damage to endocrine glands can be a diagnostic and management challenge. We aimed to review the incidence, biochemical evolution and imaging findings of endocrine toxicity related to combined anti CTLA-4 and anti-PD-1 therapy. Methods: We undertook a retrospective chart review of patients who received combined ipilimumab and nivolumab for metastatic melanoma at a tertiary referral centre between 2016-2019. We recorded onset and duration of abnormal biochemistry in endocrine irAEs, reviewed all available MRI images for pituitary size (mm) and appearance and 18-F FDG PET images for features of hypophysitis, thyroiditis and pancreatitis. Results: 162 patients received combination therapy. At least one irAE was recorded in 135 patients (83%), 100 (62%) required glucocorticoids, and 84 (52%) had an unplanned hospital presentation due to irAEs. Thyroiditis occurred in 50 (30.9%), with median time to onset of 30.9 days (range 1-234 days). 35 cases were identified with routine biochemistry performed every 4-6 weeks. TSH receptor antibody was measured in 13 patients and all were negative. 29 (58%) developed permanent hypothyroidism. Central cortisol deficiency was documented in 31 (19%) with a median time to diagnosis of 67.5 days (range 5-286). 4 cases were diagnosed on routine biochemistry and 14 presented with symptoms prompting investigation. 13 were diagnosed after routine neuroimaging demonstrated a pituitary abnormality, and a further 27 patients without the clinical syndrome had features of hypophysitis on neuroimaging. New onset diabetes occurred in 3 people, in which pancreatic inflammation on imaging was found in 2. A further 3/5 patients with an asymptomatic elevated lipase were found to have abnormal pancreatic imaging. In one patient with no features of endocrine or exocrine failure, there was a significant increase in FDG uptake and a subsequent loss of pancreatic volume. Conclusion: We report real world incidence of endocrine irAEs with combination immunotherapy. Routine biochemistry leads to the detection of some but not all cases. Early recognition and avoidance of unplanned presentations remains a challenge. Opportunistic assessment of endocrine gland appearance on routine imaging studies may provide useful early diagnostic information. Reference: Larkin J, Chiarion-Sileni V, Gonzalez R, Grob JJ, Cowey CL, Lao CD, et al. Combined nivolumab and ipilimumab or monotherapy in untreated melanoma. N Engl J Med. (2015) 1:23-34. 10.1056/NEJMoa1504030
机译:背景:免疫检查点封锁现已成为几种恶性肿瘤的护理标准。涉及联合细胞毒性T淋巴细胞相关蛋白4(CTLA4)和编程的细胞死亡蛋白1(PD1)阻断的试验表明了黑色素瘤中的改善肿瘤反应,但在55%的严重3-4免疫相关不良事件(IRAE)的成本下,并且内分泌伊拉斯高达10%[1]。免疫介导对内分泌腺的损伤可以是诊断和管理挑战。我们旨在审查与组合抗CTLA-4和抗PD-1治疗相关的内分泌毒性的发病率,生化演化和成像结果。方法:我们对2016 - 2019年间第三次推荐中心进行了患者进行了回顾性图表审查,在第三次推荐中心处于第三节推荐中心进行转移性黑色素瘤。我们记录了内分泌赤道的异常生物化学的发病和持续时间,审查了垂体尺寸(mm)和外观和18-F FDG PET图像的所有可用MRI图像,用于衰落性炎,甲状腺炎和胰腺炎的特征。结果:162名患者接受组合治疗。在135名患者(83%)中,至少有一个IRAE被记录,100(62%)所需的糖皮质激素,84名(52%)由于伊拉斯而有一个意外的医院介绍。甲状腺炎发生在50(30.9%)中,中位时间为30.9天(范围1-234天)。每4-6周进行35例常规生物化学鉴定出常规生物化学。在13名患者中测量TSH受体抗体,所有均为阴性。 29(58%)发育永久性甲状腺功能亢进。中央皮质醇缺乏在31(19%)中记录了31(19%),中位数诊断为67.5天(范围5-286)。 4例患者诊断出常规生物化学和14例,提出症状促使调查。 13常规神经影像术后诊断诊断垂体异常,还有27例没有临床综合征的患者在神经影像上具有次衰叠的特征。在3人中发生了新的发病糖尿病,其中在成像中发现了胰腺炎。发现了3/5患者的无症状升高脂肪酶具有异常胰腺成像。在一个没有内分泌或外泌体失败的患者中,FDG摄取的显着增加和随后的胰腺量丧失。结论:我们向组合免疫疗法报告了内分泌赤纬的现实世界发病率。常规生物化学导致检测一些但不是所有情况。早期承认和避免无计划的演示仍然是一个挑战。常规成像研究对内分泌腺外观的机会评估可以提供有用的早期诊断信息。参考:Larkin J,Chiarion-Sileni V,Gonzalez R,Grob Jj,Cowey Cl,老挝CD,等。组合Nivolumab和Ipilimumab或单药治疗未处理的黑色素瘤。 n Engl J Med。 (2015)1:23-34。 10.1056 / nejmoa1504030

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