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III期胸腺瘤:手术及术后放疗后的失败模式及其对未来研究的启示

Stage III thymoma: pattern of failure after surgery and postoperative radiotherapy and its implication for future study.

作者信息

Myojin M, Choi N C, Wright C D, Wain J C, Harris N, Hug E B, Mathisen D J, Lynch T, Carey R W, Grossbard M, Finkelstein D M, Grillo H C

机构信息

Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2000 Mar 1;46(4):927-33. doi: 10.1016/s0360-3016(99)00514-3.

Abstract

PURPOSE

With the conventional approach of surgery and postoperative radiotherapy for patients with Masaoka Stage III thymoma, progress has been slow for an improvement in the long-term survival rate over the past 20 years. The objective of this study was to evaluate the pattern of failure and survival after surgery and postoperative radiotherapy in Stage III thymoma and search for a new direction for better therapy outcome.

METHODS AND MATERIALS

Between 1975 and 1993, 111 patients with thymoma were treated at Massachusetts General Hospital. Of these, 32 patients were determined to have Masaoka Stage III thymoma. The initial treatment included surgery for clinically resectable disease in 25 patients and preoperative therapy for unresectable disease in 7 patients. Surgical procedure consisted of thymectomy plus resection of involved tissues. For postoperative radiotherapy (n = 23), radiation dose consisted of 45-50 Gy for close resection margins, 54 Gy for microscopically positive resection margins, and 60 Gy for grossly positive margins administered in 1.8 to 2.0 Gy of daily dose fractions, 5 fractions a week, over a period of 5 to 6.6 weeks. In preoperative radiotherapy, a dose of 40 Gy was administered in 2.0 Gy of daily dose fractions, 5 days a week. For patients with large tumor requiring more than 30% of total lung volume included in the target volume (n = 3), a preoperative radiation dose of 30 Gy was administered and an additional dose of 24-30 Gy was given to the tumor bed region after surgery for positive resection margins.

RESULTS

Patients with Stage III thymoma accounted for 29% (32/111 patients) of all patients. The median age was 57 years with a range from 27 to 81 years; gender ratio was 10:22 for male to female. The median follow-up time was 6 years. Histologic subtypes included well-differentiated thymic carcinoma in 19 (59%), high-grade carcinoma in 6 (19%), organoid thymoma in 4 (13%), and cortical thymoma in 3 (9%) according to the Marino and Müller-Hermelink classification. The overall survival rates were 71% and 54% at 5 and 10 years, respectively. Ten of the 25 patients who were subjected to surgery as initial treatment were found to have incomplete resection by histopathologic evaluation. The 5- and 10-year survival rates were 86% and 69% for patients (n = 15) with clear resection margins as compared with 28% and 14% for those (n = 10) with incomplete resection margins even after postoperative therapy, p = 0.002. Survival rates at 5 and 10 years were 100% and 67% for those with unresectable disease treated with preoperative radiation (n = 6) and subsequent surgery (n = 3). Recurrence was noted in 12 of 32 patients and 11 of these died of recurrent thymoma. Recurrences at pleura and tumor bed accounted for 77% of all relapses, and all pleural recurrences were observed among the patients who were treated with surgery initially.

CONCLUSION

Incomplete resection leads to poor results even with postoperative radiotherapy or chemoradiotherapy in Stage III thymoma. Pleural recurrence is also observed more often among patients treated with surgery first. These findings suggest that preoperative radiotherapy or chemoradiotherapy may result in an increase in survival by improving the rate of complete resection and reducing local and pleural recurrences.

摘要

目的

对于采用手术及术后放疗的常规方法治疗的Masaoka III期胸腺瘤患者,在过去20年中,长期生存率的改善进展缓慢。本研究的目的是评估III期胸腺瘤手术及术后放疗后的失败模式和生存率,并寻找改善治疗效果的新方向。

方法与材料

1975年至1993年期间,麻省总医院治疗了111例胸腺瘤患者。其中,32例患者被确定为Masaoka III期胸腺瘤。初始治疗包括25例临床可切除疾病患者的手术治疗和7例不可切除疾病患者的术前治疗。手术程序包括胸腺切除术及受累组织切除术。对于术后放疗(n = 23),放疗剂量为切缘阴性者45 - 50 Gy,镜下切缘阳性者54 Gy,肉眼切缘阳性者60 Gy,每日剂量分割为1.8至2.0 Gy,每周5次,持续5至6.6周。在术前放疗中,每日剂量分割为2.0 Gy,每周5天,给予40 Gy剂量。对于肿瘤体积较大,靶体积包含超过30%全肺体积的患者(n = 3),术前放疗剂量为30 Gy,术后切缘阳性时,肿瘤床区域追加24 - 30 Gy剂量。

结果

III期胸腺瘤患者占所有患者的29%(32/111例患者)。中位年龄为57岁,范围为27至81岁;男女比例为10:22。中位随访时间为6年。根据马里诺和米勒 - 赫梅林克分类,组织学亚型包括高分化胸腺癌19例(59%)、高级别癌6例(19%)、类器官胸腺瘤4例(13%)和皮质胸腺瘤3例(9%)。5年和10年的总生存率分别为71%和54%。25例初始接受手术治疗的患者中,10例经组织病理学评估发现切除不完全。切缘阴性患者(n = 15)的5年和10年生存率分别为86%和69%,而切缘不完全患者(n = 10)即使经过术后治疗,5年和10年生存率分别为28%和14%,p = 0.002。术前放疗(n = 6)及随后手术(n = 3)治疗的不可切除疾病患者,5年和10年生存率分别为100%和67%。32例患者中有12例出现复发,其中11例死于复发性胸腺瘤。胸膜和肿瘤床复发占所有复发的77%,所有胸膜复发均见于初始接受手术治疗的患者。

结论

在III期胸腺瘤中,即使进行术后放疗或放化疗,切除不完全也会导致不良结果。在首先接受手术治疗的患者中,胸膜复发也更常见。这些发现表明,术前放疗或放化疗可能通过提高完全切除率和减少局部及胸膜复发而提高生存率。

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