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原发性心包间皮瘤患者的多模态治疗。

Multimodality Therapy in Patients With Primary Pericardial Mesothelioma.

机构信息

Thoracic Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; Department of Medicine, Weill Cornell Medical College, New York, New York.

Thoracic Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

J Thorac Oncol. 2022 Dec;17(12):1428-1432. doi: 10.1016/j.jtho.2022.08.017. Epub 2022 Sep 6.

Abstract

INTRODUCTION

Primary pericardial mesothelioma (PPM) has no accepted standard-of-care treatment options with management and outcomes often extrapolated from diffuse pleural mesothelioma. Disease-specific research is needed to better define PPM. We report our institutional experience with PPM highlighting the potential role for multimodality therapy.

METHODS

Patients with PPM diagnosed by a multidisciplinary team of medical oncologists, thoracic surgeons, thoracic pathologists, and radiologists between January 2011 and January 2022 were followed to February 2022. Clinicopathologic features and treatment outcomes were annotated. Overall survival (OS) was defined from the date of pathologic diagnosis.

RESULTS

The median age at diagnosis of the 12 patients identified with having PPM was 51 (range: 21-71) years old. Most patients were of female sex (n = 8; 67%), 75% of the samples were epithelioid (n = 9), and 25% were nonepithelioid (two sarcomatoid and one biphasic). Most cases (92%, 11 of 12) had expression of at least two mesothelial markers on immunohistochemistry. The median OS of the cohort was 25.9 months. Five patients had an OS greater than 12 months; four of whom received pericardial radiation. Three of the patients who received radiation did so as part of a trimodality approach (surgical resection, adjuvant chemotherapy, and radiation); the OS for patients who received trimodality therapy was 70.3 months versus 8.2 months for those who did not.

CONCLUSIONS

PPM represents a distinct disease with no universally accepted treatment options. Our findings suggest that trimodality therapy may improve outcomes in selected patients with PPM.

摘要

简介

原发性心包间皮瘤(PPM)尚无标准治疗方法,其治疗和预后通常是从弥漫性胸膜间皮瘤中推断出来的。需要进行疾病特异性研究以更好地定义 PPM。我们报告了我们机构在 PPM 方面的经验,重点强调了多模态治疗的潜在作用。

方法

2011 年 1 月至 2022 年 1 月,多学科医疗肿瘤学家、胸外科医生、胸病理学家和放射科医生组成的团队诊断出 12 例 PPM 患者,对这些患者进行了随访,随访时间截至 2022 年 2 月。对患者的临床病理特征和治疗结果进行了注释。总生存期(OS)定义为病理诊断日期。

结果

12 例 PPM 患者的中位年龄为 51 岁(范围:21-71 岁)。大多数患者为女性(n=8;67%),75%的样本为上皮样(n=9),25%为非上皮样(2 例肉瘤样和 1 例双相型)。大多数病例(92%,11/12)的免疫组化至少表达两种间皮标志物。该队列的中位 OS 为 25.9 个月。5 例患者的 OS 超过 12 个月;其中 4 例接受了心包放疗。接受放疗的 3 例患者采用了三联治疗方法(手术切除、辅助化疗和放疗);接受三联治疗的患者 OS 为 70.3 个月,而未接受治疗的患者 OS 为 8.2 个月。

结论

PPM 是一种独特的疾病,目前尚无普遍接受的治疗方法。我们的研究结果表明,三联疗法可能会改善特定 PPM 患者的预后。

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Multimodality Therapy in Patients With Primary Pericardial Mesothelioma.原发性心包间皮瘤患者的多模态治疗。
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