Surgical Management of Primary and Metastatic Cardiac Malignancies: A 20-Year Single-Center Experience.

IF 1.3
Ryo Nakanishi, Hiroto Kawakami, Naoto Tanabe, Koki Tamaoka, Akira Takeuchi, Shoichi Kyo, Tomofumi Taki, Hiroshi Tsuneyoshi
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Abstract

Purpose: Malignant cardiac tumors are rare and have a poor prognosis. Surgical resection is performed for symptom relief and survival benefit, but its efficacy is limited. We reviewed our 20-year single-institution experience with primary and metastatic malignant cardiac tumors.

Methods: We retrospectively reviewed 15 patients who underwent resection for histologically confirmed malignant cardiac tumors between 2006 and 2025. Data included tumor characteristics, resection status, and survival outcomes.

Results: Of 15 patients, 7 (46.7%) had primary tumors (most common: angiosarcoma) and 8 (53.3%) had metastatic lesions. The right atrium was the most frequent site (60.0%). Complete (R0) resection was achieved in only 3 cases (20.0%). Median overall survival (OS) for the cohort was 11 months. Patients with angiosarcoma had particularly poor outcomes (median OS: 5 months). One patient with metastatic thymic carcinoma achieved long-term survival (>15 years) following multimodal therapy. Adjuvant therapy was administered in 7 patients (46.7%). No 30-day postoperative mortality occurred.

Conclusion: Surgical resection of malignant cardiac tumors is feasible with acceptable perioperative safety. Although R0 resection is rarely attainable and long-term outcomes remain poor, particularly for high-grade sarcomas, a multimodal approach is essential to optimize outcomes in selected patients.

原发性和转移性心脏恶性肿瘤的外科治疗:20年的单中心经验。
目的:恶性心脏肿瘤少见,预后差。手术切除是为了缓解症状和改善生存,但其疗效有限。我们回顾了20年来在单一机构治疗原发性和转移性恶性心脏肿瘤的经验。方法:我们回顾性分析了2006年至2025年间15例经组织学证实的恶性心脏肿瘤切除术患者。数据包括肿瘤特征、切除状态和生存结果。结果:15例患者中,7例(46.7%)为原发肿瘤(最常见的为血管肉瘤),8例(53.3%)为转移性病变。右心房是最常见的部位(60.0%)。完全(R0)切除仅3例(20.0%)。队列的中位总生存期(OS)为11个月。血管肉瘤患者的预后尤其差(中位生存期:5个月)。一名转移性胸腺癌患者在接受多模式治疗后获得了长期生存期(约15年)。辅助治疗7例(46.7%)。无术后30天死亡率。结论:手术切除心脏恶性肿瘤是可行的,围手术期安全性可接受。尽管R0切除术很少实现,长期预后仍然很差,特别是对于高级别肉瘤,多模式方法对于优化选定患者的预后至关重要。
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