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胸腺瘤伴胸膜播散患者的多模态治疗

Multimodality therapy for thymoma patients with pleural dissemination.

作者信息

Nakamura Shota, Kawaguchi Koji, Fukui Takayuki, Hakiri Shuhei, Ozeki Naoki, Mori Shunsuke, Goto Masaki, Hashimoto Kumiko, Ito Toshinari, Yokoi Kohei

机构信息

Department of Thoracic Surgery, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan.

出版信息

Gen Thorac Cardiovasc Surg. 2019 Jun;67(6):524-529. doi: 10.1007/s11748-018-01054-7. Epub 2019 Feb 6.

Abstract

BACKGROUND

Although multidisciplinary treatment is recommended for patients with advanced stage and recurrent thymoma, a detailed treatment strategy remains controversial. We have performed a multimodality therapy of induction chemotherapy (CAMP therapy: cisplatin, doxorubicin, and methylprednisolone) combined with surgery for those patients. We now conducted a retrospective study for investigating the results of this multimodality therapy for thymoma patients with pleural dissemination.

PATIENTS AND METHODS

Between 2003 and 2017, 201 patients underwent surgical resection for thymomas. Twenty-six of them received induction CAMP therapy followed by surgery, and 19 of them with pleural dissemination were enrolled in this study. Those cohort were divided into 2 groups by employing surgical procedures: extrapleural pneumonectomy (EPP) group (n = 10) and resection of plural dissemination (RPD) group (n = 9).

RESULTS

The median age of all patients was 49 years. Based on the WHO classification, the histological diagnoses of those thymomas were as follows: Type B1 (n = 1), Type B2 (n = 13), and Type B3 (n = 5). Seven patients were complicated with myasthenia gravis (MG). Clinical stage of the 13 primary cases based on the Masaoka classification were stage IV, and the remaining six cases had recurrent pleural dissemination after surgery. Partial response in induction CAMP therapy was obtained in 78.9% (n = 15) of the patients. Adverse events (Grade 4) occurred in 2 patients (10.5%). Postoperative complications (Grade 4) were observed in 2 patients (10.5%). In all of the enrolled patients, the five-year overall survival rate (5Y-OS) and 5-year progression-free survival rate (5Y-PFS) were 76.7% and 55.1%, respectively. In the EPP group, 5Y-OS and 5Y-PFS were 83.3% and 83.3%, respectively, and in the RPD group, 70.0% and 29.6%, respectively.

CONCLUSIONS

Multidisciplinary treatment using induction CAMP therapy and surgical resection for thymoma patients with pleural dissemination was effective and feasible. Because of the low recurrent rate of disease, young patients with good cardiopulmonary function and well-controlled MG might be good candidates for EPP.

摘要

背景

尽管对于晚期和复发性胸腺瘤患者推荐采用多学科治疗,但详细的治疗策略仍存在争议。我们对这些患者实施了诱导化疗(CAMP疗法:顺铂、阿霉素和甲基强的松龙)联合手术的多模式治疗。我们现在进行了一项回顾性研究,以调查这种多模式治疗对伴有胸膜播散的胸腺瘤患者的效果。

患者与方法

2003年至2017年间,201例患者接受了胸腺瘤手术切除。其中26例接受了诱导CAMP治疗后再进行手术,本研究纳入了其中19例伴有胸膜播散的患者。根据手术方式将这些队列分为2组:胸膜外全肺切除术(EPP)组(n = 10)和胸膜播散切除术(RPD)组(n = 9)。

结果

所有患者的中位年龄为49岁。根据世界卫生组织分类,这些胸腺瘤的组织学诊断如下:B1型(n = 1)、B2型(n = 13)和B3型(n = 5)。7例患者合并重症肌无力(MG)。根据Masaoka分类,13例原发性病例的临床分期为IV期,其余6例术后出现复发性胸膜播散。78.9%(n = 15)的患者在诱导CAMP治疗中获得部分缓解。2例患者(10.5%)发生4级不良事件。2例患者(10.5%)观察到4级术后并发症。在所有纳入患者中,5年总生存率(5Y-OS)和5年无进展生存率(5Y-PFS)分别为76.7%和55.1%。在EPP组中,5Y-OS和5Y-PFS分别为83.3%和83.3%,在RPD组中分别为70.0%和29.6%。

结论

对于伴有胸膜播散的胸腺瘤患者,采用诱导CAMP治疗和手术切除的多学科治疗是有效且可行的。由于疾病复发率低,心肺功能良好且MG控制良好的年轻患者可能是EPP的良好候选者。

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