Nuclear Medicine and Endocrine Oncology Department, Maria Skłodowska-Curie Memorial Cancer Centre and Institute of Oncology, Gliwice Branch, Poland.
Endokrynol Pol. 2010 Sep-Oct;61(5):492-6.
Papillary thyroid cancer (PTC) usually has a good prognosis. The treatment, including total thyroidectomy and complementary radioiodine (RAI) therapy, gives complete remission in 90% of patients. However, in 10% of subjects with metastatic disease, the prognosis is poor. In the group of patients with disease progression and no 131I uptake, searching for new therapeutic modalities before all tyrosine kinase inhibitors and other antiangiogenic agents is necessary. The study presents the case of a 55-year-old male with advanced PTC /pT3mNxMo/ diagnosed in 1993. Primary treatment by total thyroidectomy and 131I ablation led to complete remission. In 2000 local as well as lymph node recurrence was diagnosed and successively treated by surgery. In 2006 an increasing serum thyroglobulin level was noted and a single lung metastasis was diagnosed and operated on. In 2007 new foci in CNS and vertebral column with no 131I uptake were stated. Further progression (bones, CNS, and pterygoid muscle) was confirmed by PET-CT. The patient underwent neurosurgical metastasectomy twice and palliative CNS and vertebra's radiotherapy. Liver metastases were diagnosed in 2009. Treatment with increasing doses of thalidomide (up to 800 mg/d) was administered for 3 months with a good tolerance; however, the therapy was withdrawn due to cancer progression. Next, sorafenib (800 mg/d) was given for 16 weeks. Radiological examination performed after 16 weeks confirmed stable disease, whereas 2 months later, after sorafenib withdrawal due to lack of treatment possibility, further progression was observed. Metronomic chemotherapy with Adriamycin was instituted which gave disease stabilization for 6 months. The patient died with advanced disseminated disease due to pulmonary embolism. We present this case to document no adverse effects of therapy with sorafenib in a patient with brain DTC metastases. Sorafenib therapy was only short-term, but no progression occurred in this time.
甲状腺乳头状癌(PTC)通常预后良好。包括甲状腺全切除术和补充放射性碘(RAI)治疗在内的治疗方法,使 90%的患者获得完全缓解。然而,在 10%有转移疾病的患者中,预后较差。对于疾病进展且无 131I 摄取的患者组,在使用所有酪氨酸激酶抑制剂和其他抗血管生成药物之前,有必要寻找新的治疗方法。本研究介绍了一名 55 岁男性患者的病例,他于 1993 年被诊断为晚期 PTC/pT3mNxMo/。甲状腺全切除术和 131I 消融术的初始治疗使疾病完全缓解。2000 年诊断出局部和淋巴结复发,并相继通过手术治疗。2006 年,发现血清甲状腺球蛋白水平升高,诊断出单个肺转移灶并进行了手术。2007 年,新发现 CNS 和脊柱无 131I 摄取的病灶。进一步的进展(骨骼、CNS 和翼状肌)通过 PET-CT 得到证实。患者接受了两次神经外科转移灶切除术和姑息性 CNS 和脊柱放疗。2009 年诊断出肝转移。使用沙利度胺(高达 800mg/d)进行递增剂量治疗 3 个月,耐受性良好;然而,由于癌症进展,治疗被停止。随后,给予索拉非尼(800mg/d)治疗 16 周。16 周后进行的影像学检查确认疾病稳定,然而,在索拉非尼停药 2 个月后,由于缺乏治疗可能性,观察到进一步进展。开始进行阿霉素的节拍化疗,使疾病稳定 6 个月。由于肺栓塞,患者死于晚期广泛转移的疾病。我们介绍这个病例是为了证明索拉非尼治疗脑 DTC 转移患者没有不良反应。索拉非尼治疗时间很短,但在此期间没有进展。