免疫检查点疗法治疗心脏转移患者的安全性和有效性:一项多中心国际回顾性研究。

IF 10.3 1区 医学 Q1 IMMUNOLOGY
Amin H Nassar, Sarah Abou Alaiwi, Talal El Zarif, Ryan Denu, Walid Macaron, Noha Abdel-Wahab, Dory Freeman, Alexi Vasbinder, Salim Hayeck, Elizabeth Anderson, Rachel S Goodman, Douglas B Johnson, Shirly Grynberg, Ronnie Shapira, Jennifer M Kwan, Rachel Woodford, Georgina V Long, Tarek Haykal, Susan Dent, Yuki Kojima, Kan Yonemor, Ankita Tandon, Alexandra Trevino, Nausheen Akhter, Eric H Yang, Gavin Hui, Alexandra Drakaki, Edward El-Am, Elie Kozaily, Ahmad Al-Hader, Elias Bou Farhat, Priyanka Babu, Arjun Mittra, Mingjia Li, Nicholas Jones, Javier Baena, Mercedes Juarez Herrera, Simone Foderaro, Frank Aboubakar Nana, Chul Kim, Paul Sackstein, Kaushal Parikh, Aakash P Desai, Caleb Smith, Alessio Cortellini, David J Pinato, James Korolewicz, Nerea Lopetegui-Lia, Pauline Funchain, Arrush Choudhary, Aarti Asnani, Vishal Navani, Daniel Meyers, Igor Stukalin, Jesus Antonio Ocejo Gallegos, Jonathan Trent, Sanober Nusrat, Carmel Malvar, Rana R McKay, Tomas G Neilan, Toni K Choueiri, Abdul Rafeh Naqash
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Patients who had received ≥1 dose of ICI were included. Treatment-related adverse events (trAEs) were graded per Common Terminology Criteria for Adverse Event V.5.0. Objective response rates (ORR) were evaluated by Response Evaluation Criteria in Solid Tumors V.1.1 when available. Overall survival (OS) and progression-free survival (PFS) were estimated by the Kaplan-Meier method.</p><p><strong>Results: </strong>Among 110 pts, median age at ICI initiation was 65 (IQR: 59-75). Median follow-up time since ICI initiation was 36 (95% CI: 26 to 51) months. Melanoma (38%, n=42) and non-small cell lung cancer (24%, n=26) were the most common. 68 (62%) patients received ICIs as first-line, and 29 (26%) patients were treated with combination anti-programmed death-1 and anti-cytotoxic T-lymphocyte antigen 4. 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引用次数: 0

摘要

背景:使用免疫检查点抑制剂(ICIs)治疗实体瘤和心脏转移患者的安全性和临床结果数据有限。方法:这是一项国际多中心回顾性研究,在基线时对癌症和心脏转移患者进行研究。患者接受了≥1剂量的ICI。治疗相关不良事件(trAEs)按照不良事件通用术语标准V.5.0进行分级。客观缓解率(ORR)根据实体瘤应答评价标准(response Evaluation Criteria in Solid Tumors V.1.1)评估。用Kaplan-Meier法估计总生存期(OS)和无进展生存期(PFS)。结果:在110名患者中,ICI开始时的中位年龄为65岁(IQR: 59-75)。ICI开始后的中位随访时间为36个月(95% CI: 26 ~ 51)。黑色素瘤(38%,n=42)和非小细胞肺癌(24%,n=26)是最常见的。68例(62%)患者接受ICIs作为一线治疗,29例(26%)患者联合抗程序性死亡1和抗细胞毒性t淋巴细胞抗原4治疗。心脏转移最常见的部位是心房(37%,n=41)和心室(35%,n=39)。双侧心/心包转移15例(13.6%),左侧44例(40%),右侧43例(39.8%)。在ICI开始时,21% (n=23)有心脏血栓。分别有58例(53%)和52例(47%)患者在癌症诊断时完成了心脏病学转诊和心脏mri。40例(36%)患者发生心脏事件,包括心律失常(n=14, 13%)、动脉/静脉栓塞(n=4, 3.6%)和心包填塞(n=3, 2.7%)。53例(47%)患者发生trae;最常见的是结肠炎/腹泻(n=16, 15%)、皮炎(n=13, 12%)和肝炎(n=9, 8.2%)。2例(1.8%)患者发生ici相关的主要心脏trae。22例(20%)发生≥3级trAE。多发心脏转移患者与单一心脏转移患者相比,对基于ci的方案的反应明显较低(11% vs 63%, p=0.02)。对于黑色素瘤,ORR、中位PFS和中位OS分别为38%、9.0个月和28.9个月。83%的黑色素瘤患者在总体疾病负担和心脏病方面有一致的反应。91例患者停止使用ICIs, 55例(49%)患者的主要原因是进展或死亡。结论:在既往存在心脏转移的患者中,ICIs显示出有意义的临床疗效,没有增加安全性信号。大多数患者在总体疾病负担和心脏质量方面有一致的反应。多学科团队对心脏转移患者的适当治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety and efficacy of immune checkpoint therapy for the treatment of patients with cardiac metastasis: a multicenter international retrospective study.

Background: Data on the safety profiles and clinical outcomes of patients with solid tumors and cardiac metastasis treated with immune checkpoint inhibitors (ICIs) are limited.

Methods: This is an international multicenter retrospective study of patients with cancer and cardiac metastasis at baseline. Patients who had received ≥1 dose of ICI were included. Treatment-related adverse events (trAEs) were graded per Common Terminology Criteria for Adverse Event V.5.0. Objective response rates (ORR) were evaluated by Response Evaluation Criteria in Solid Tumors V.1.1 when available. Overall survival (OS) and progression-free survival (PFS) were estimated by the Kaplan-Meier method.

Results: Among 110 pts, median age at ICI initiation was 65 (IQR: 59-75). Median follow-up time since ICI initiation was 36 (95% CI: 26 to 51) months. Melanoma (38%, n=42) and non-small cell lung cancer (24%, n=26) were the most common. 68 (62%) patients received ICIs as first-line, and 29 (26%) patients were treated with combination anti-programmed death-1 and anti-cytotoxic T-lymphocyte antigen 4. The most common location of cardiac metastasis was in the atria (37%, n=41) and ventricles (35%, n=39). 15 patients (13.6%) had bilateral cardiac/pericardial metastasis, 44 (40%) had left-sided, and 43 (39.8%) had right-sided. At ICI initiation, 21% (n=23) had a cardiac thrombus. Cardiology referrals and cardiac MRIs at the time of cancer diagnosis were completed on 58 (53%) and 52 (47%) patients, respectively. Cardiac events occurred in 40 (36%) patients, including arrhythmias (n=14, 13%), arterial/venous emboli (n=4, 3.6%), and cardiac tamponade (n=3, 2.7%). 53 (47%) patients developed trAEs; most common were colitis/diarrhea (n=16, 15%), dermatitis (n=13, 12%), and hepatitis (n=9, 8.2%). ICI-related major cardiac trAEs occurred in 2 (1.8%) patients. 22 patients (20%) developed grade ≥3 trAE. Patients with multiple cardiac metastases had significantly lower responses to ICI-based regimens compared with patients with single cardiac metastasis (11% vs 63%, p=0.02). For melanoma, ORR, median PFS, and median OS were 38%, 9.0 months, and 28.9 months, respectively. 83% of patients with melanoma had concordant responses in overall disease burden and cardiac disease. 91 patients discontinued ICIs, and the main reason was progression or death in 55 (49%) patients.

Conclusions: Among patients with pre-existing cardiac metastasis, ICIs demonstrated meaningful clinical efficacy with no increase in safety signals. Most patients had concordant responses in the overall disease burden and cardiac mass. Multidisciplinary teams are crucial for the appropriate management of patients with cardiac metastasis.

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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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