Yokoi Kohei, Matsuguma Haruhisa, Nakahara Rie, Kondo Tetsuro, Kamiyama Yukari, Mori Kiyoshi, Miyazawa Naoto
Division of Thoracic Surgery, Tochigi Cancer Center, Utsunomiya, Tochigi, Japan.
J Thorac Oncol. 2007 Jan;2(1):73-8. doi: 10.1097/JTO.0b013e31802bafc8.
Advanced invasive thymomas are not usually manageable by surgical resection and radiotherapy. We reviewed our experience with a multidisciplinary approach and evaluated chemotherapy in the treatment of invasive thymoma.
Seventeen consecutive patients with invasive thymoma were treated with multimodality therapy consisting of chemotherapy, surgery, and/or radiotherapy. Four patients had stage III disease with superior vena cava invasion, nine had stage IVa disease, and four had stage IVb disease. The chemotherapy regimen consisted of cisplatin, doxorubicin, and methylprednisolone (CAMP). Chemotherapy was administered in a neoadjuvant setting to the 14 patients and in an adjuvant setting to the remaining three patients. Surgical resection was intended in all patients. After those treatments, chemotherapy and/or radiation therapy were performed.
All but one of the 14 patients with induction chemotherapy responded to the CAMP therapy, and the response rate was 92.9%. Seven of these patients underwent complete remission after surgical resection and chemoradiotherapy, and the others underwent partial remission. All three patients treated with surgical resection and then chemotherapy with or without radiotherapy also achieved complete remission. Tumor progression after multimodality therapy occurred in 10 patients. After retreatment, eight of these patients were alive at the time of analysis, with a median survival time after recurrence of 30 months. The 5- and 10-year overall survival rates for all patients were both 80.7%. The major side effect of CAMP therapy was acceptable neutropenia.
CAMP therapy was highly effective for invasive thymomas, and the multimodality therapy containing this chemotherapy brought about good disease control in the majority of patients. We believe that this multidisciplinary treatment with CAMP therapy, surgery, and radiotherapy is a justifiable initial treatment for patients with advanced invasive thymoma. Furthermore, appropriate treatments are essential for the long-term survival of patients with recurrences after multimodality therapy.
晚期侵袭性胸腺瘤通常无法通过手术切除和放疗进行有效治疗。我们回顾了多学科治疗方法的经验,并评估了化疗在侵袭性胸腺瘤治疗中的作用。
17例连续的侵袭性胸腺瘤患者接受了包括化疗、手术和/或放疗的多模式治疗。4例患者为Ⅲ期疾病伴上腔静脉侵犯,9例为Ⅳa期疾病,4例为Ⅳb期疾病。化疗方案包括顺铂、阿霉素和甲基强的松龙(CAMP)。14例患者接受新辅助化疗,其余3例接受辅助化疗。所有患者均计划进行手术切除。在这些治疗后,进行化疗和/或放疗。
14例接受诱导化疗的患者中,除1例患者外,其余均对CAMP治疗有反应,缓解率为92.9%。其中7例患者在手术切除和放化疗后完全缓解,其余患者部分缓解。3例接受手术切除然后接受化疗(无论是否联合放疗)的患者也均实现完全缓解。多模式治疗后10例患者出现肿瘤进展。再次治疗后,分析时其中8例患者存活,复发后的中位生存时间为30个月。所有患者的5年和10年总生存率均为80.7%。CAMP治疗的主要副作用为可接受的中性粒细胞减少。
CAMP治疗对侵袭性胸腺瘤高度有效,包含这种化疗的多模式治疗在大多数患者中实现了良好的疾病控制。我们认为,这种采用CAMP治疗联合手术和放疗的多学科治疗是晚期侵袭性胸腺瘤患者合理的初始治疗方法。此外,适当的治疗对于多模式治疗后复发患者的长期生存至关重要。