AB014.奥曲肽扫描未摄取的晚期胸腺瘤患者的有效生长抑素类似物

X. Mielgo-Rubio, S. Hernando Polo, Elisabeth Jiménez Aguilar, C. Olier Garate, Alicia Hurtado Nuño, D. Moreno Muñoz, Maria Virginia Sánchez Becerra, A. G. González López, Mónica Esteban García, Teresa Robles Bermejo, M. Barón, F. Hernando Trancho, Jose Ramón Jarabo, Juan Carlos Cámara Vicario
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引用次数: 0

摘要

背景由于缺乏随机试验的证据,晚期恶性胸腺瘤的治疗非常具有挑战性。尽管病情严重且无法治愈,但大多数患者的生存期很长,他们通常会接受多种治疗。没有标准的第二条线,对于这些长期存活的患者,应考虑化疗(CT)的毒性。生长抑素类似物治疗难治性复发性和/或转移性胸腺瘤显示出疗效。病例描述2010年1月,一名31岁的女性被诊断为前纵隔肿块,活检符合胸腺瘤B3和重症肌无力。胸腺瘤在新辅助CT(缩写:顺铂、阿霉素、长春新碱和环磷酰胺(ADOC)方案)两个周期后切除,然后接受额外的辅助ADOC。疾病于2012年11月进展,胸膜植入物和右上叶肺结节。在使用卡铂和依托泊苷进行6个周期的全身CT检查并出现主要部分反应后,她于2013年11月和2014年3月进行了两次手术,切除了肺部和胸膜的残余疾病。14个月后(2015年5月),新的胸膜疾病进展后,新的手术切除被取消,并接受了几轮卡铂和依托泊苷的再治疗,其间有休息期。在每次CT检查后,患者都会出现肿瘤反应,但在最后一个周期,她开始出现严重的骨髓毒性。在2021年11月最后一次显著进展后,决定评估CT的低毒替代治疗方案,尽管奥曲肽扫描中没有摄取,但根据RECISTv1标准(迄今为止9个月的无进展期)和良好的耐受性,奥曲肽每28天30 mg IM开始实现稳定的疾病。诊断:晚期胸腺瘤伴胸膜复发的长期存活患者接受了几轮化疗,对奥曲肽有反应,而不是在奥曲肽扫描中没有摄取。结论无论奥曲肽扫描摄取量如何,生长抑素类似物均可作为经预处理的晚期胸腺瘤患者的低毒治疗选择。这种治疗方法应在前瞻性临床试验中进行研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
AB014. Effective somatostatin analogs in a case of advanced thymoma with no uptake in the octreotide scan
Background Management of advanced malignant thymoma is very challenging due to the lack of evidence from randomized trials. Despite advanced and non-curable status, most patients achieve long survival and they usually receive several treatment lines along their disease. There is no standard second line, and toxicity of chemotherapy (CT) should be considered for these long survivors. Treatment with somatostatin analogs showed efficacy in patients with refractory recurrent and/or metastatic thymomas. Case Description In January 2010, a 31-year-old woman was diagnosed of a mass in the anterior mediastinum with a biopsy compatible with thymoma B3 and myasthenia gravis. Thymoma was resected after 2 cycles of neoadjuvant CT with acronym: cisplatin, doxorrubicin, vincristine and cyclophosphamide (ADOC) schedule, then she received additional adjuvant ADOC. Disease progressed on November 2012 with pleural implants and lung nodule in upper right lobe. After 6 cycles of systemic CT with carboplatin and etoposide and major partial response, she was operated on twice on November 2013 and March 2014 with resection of residual disease in lung and pleura. After new pleural disease progression 14 months later (May 2015), new surgical resection was dismissed and received several rounds of retreatment with carboplatin and etoposide with rest periods between them. After each course of this CT, the patient presented a tumor response, but in the last cycles she began to present significant bone marrow toxicity. After the last significant progression in November 2021, it was decided to assess a low-toxic treatment alternative to CT, and despite no uptake in the octreotide scan, octreotide 30 mg IM every 28 days was started achieving stable disease according to RECISTv1 criteria (progression-free interval of 9 months to date) and good tolerance. Diagnosis: long survivor patient with advanced thymoma with pleural relapsing disease treated with several rounds of chemotherapy and response to octreotide instead of no uptake in the octreotide scan. Conclusions Somatostatin analogs can be a low-toxic treatment option in pretreated advanced thymoma patients regardless the octreotide scan uptake. This treatment should be studied in prospective clinical trials.
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