Clinical Outcomes Among Immunotherapy-Treated Patients With Primary Cardiac Soft Tissue Sarcomas

IF 12 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Jacc: Cardiooncology Pub Date : 2024-02-01 DOI:10.1016/j.jaccao.2023.11.007
Amin H. Nassar MD , Edward El-Am MD , Ryan Denu MD , Sarah Abou Alaiwi MD , Talal El Zarif MD , Walid Macaron MD , Noha Abdel-Wahab MD, PhD , Aakash Desai MD , Caleb Smith MD , Kaushal Parikh MD , Muhannad Abbasi MD , Elias Bou Farhat MD , James M. Williams MD , Jeremy D. Collins MD , Ahmad Al-Hader MD , Rana R. McKay MD , Carmel Malvar MD , Mohamad Sabra MD , Caiwei Zhong MS , Raquelle El Alam MD , Abdul Rafeh Naqash MD
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Abstract

Background

Primary cardiac soft tissue sarcomas (CSTS) affect young adults, with dismal outcomes.

Objectives

The aim of this study was to investigate the clinical outcomes of patients with CSTS receiving immune checkpoint inhibitors (ICIs).

Methods

A retrospective, multi-institutional cohort study was conducted among patients with CSTS between 2015 and 2022. The patients were treated with ICI-based regimens. The Kaplan-Meier method was used to estimate overall survival (OS) and progression-free survival (PFS). Objective response rates were determined according to Response Evaluation Criteria in Solid Tumors version 1.1. Treatment-related adverse events were graded per the Common Terminology Criteria for Adverse Events version 5.0.

Results

Among 24 patients with CSTS, 17 (70.8%) were White, and 13 (54.2%) were male. Eight patients (33.3%) had angiosarcoma. At the time of ICI treatment, 18 patients (75.0%) had metastatic CSTS, and 4 (16.7%) had locally advanced disease. ICIs were administered as the first-line therapy in 6 patients (25.0%) and as the second-line therapy or beyond in 18 patients (75.0%). For the 18 patients with available response data, objective response rate was 11.1% (n = 2 of 18). The median PFS and median OS in advanced and metastatic CSTS (n = 22) were 5.7 months (95% CI: 2.8-13.3 months) and 14.9 months (95% CI: 5.7-23.7 months), respectively. The median PFS and OS were significantly shorter in patients with cardiac angiosarcomas than in those with nonangiosarcoma CSTS: median PFS was 1.7 vs 11 months, respectively (P < 0.0001), and median OS was 3.0 vs 24.0 months, respectively (P = 0.008). Any grade treatment-related adverse events occurred exclusively in the 15 patients with nonangiosarcoma CSTS (n = 7 [46.7%]), of which 6 (40.0%) were grade ≥3.

Conclusions

Although ICIs demonstrate modest activity in CSTS, durable benefit was observed in a subset of patients with nonangiosarcoma, albeit with higher toxicity.

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接受免疫疗法治疗的原发性心脏软组织肉瘤患者的临床疗效
背景原发性心脏软组织肉瘤(CSTS)多发于青壮年,且预后不佳。目的本研究旨在调查接受免疫检查点抑制剂(ICIs)治疗的CSTS患者的临床预后。方法对2015年至2022年间的CSTS患者进行了一项回顾性、多机构队列研究。这些患者接受了以 ICI 为基础的治疗方案。采用卡普兰-梅耶法估算总生存期(OS)和无进展生存期(PFS)。客观反应率根据实体瘤反应评估标准1.1版确定。24名CSTS患者中,17名(70.8%)为白人,13名(54.2%)为男性。8名患者(33.3%)患有血管肉瘤。在接受 ICI 治疗时,18 名患者(75.0%)为转移性 CSTS,4 名患者(16.7%)为局部晚期疾病。6 名患者(25.0%)将 ICI 作为一线疗法,18 名患者(75.0%)将 ICI 作为二线或二线以上疗法。在18例有反应数据的患者中,客观反应率为11.1%(18例中有2例)。晚期和转移性 CSTS(22 人)的中位生存期和中位 OS 分别为 5.7 个月(95% CI:2.8-13.3 个月)和 14.9 个月(95% CI:5.7-23.7 个月)。心脏血管肉瘤患者的中位生存期和OS明显短于非血管肉瘤CSTS患者:中位生存期分别为1.7个月和11个月(P < 0.0001),中位OS分别为3.0个月和24.0个月(P = 0.008)。任何级别的治疗相关不良事件仅发生在15例非血管肉瘤CSTS患者中(n = 7 [46.7%]),其中6例(40.0%)为≥3级。结论尽管ICIs在CSTS中表现出适度的活性,但在非血管肉瘤患者中观察到了持久的获益,尽管毒性较高。
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来源期刊
CiteScore
12.50
自引率
6.30%
发文量
106
期刊介绍: JACC: CardioOncology is a specialized journal that belongs to the esteemed Journal of the American College of Cardiology (JACC) family. Its purpose is to enhance cardiovascular care for cancer patients by publishing high-quality, innovative scientific research and sharing evidence-based knowledge. The journal aims to revolutionize the field of cardio-oncology and actively involve and educate professionals in both cardiovascular and oncology fields. It covers a wide range of topics including pre-clinical, translational, and clinical research, as well as best practices in cardio-oncology. Key areas of focus include understanding disease mechanisms, utilizing in vitro and in vivo models, exploring novel and traditional therapeutics (across Phase I-IV trials), studying epidemiology, employing precision medicine, and investigating primary and secondary prevention. Amyloidosis, cardiovascular risk factors, heart failure, and vascular disease are some examples of the disease states that are of particular interest to the journal. However, it welcomes research on other relevant conditions as well.
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