名古屋市立大学医院及相关机构lenvatinib治疗不可切除甲状腺癌的临床分析

Q4 Medicine
Gaku Takano, D. Kawakita, T. Matoba, Keisuke Oguri, Akihiro Murashima, K. Minohara, H. Tsuge, Ayano Matsumura, Wataru Hojo, Koji Tsukamoto, Ikuma Harata, S. Maseki, Taijiro Ozawa, Shoji Mitsuya, K. Moribe, Shin-ichi Iwasaki
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引用次数: 0

摘要

Lenvatinib是一种分子靶向药物,适用于不可切除的放射性碘难治性甲状腺癌,但尚未建立治疗预后的预测因子。在本研究中,我们回顾性回顾了名古屋市立大学医院及相关机构使用lenvatinib治疗的30例不可切除甲状腺癌的组织病理学特征和临床因素,并分析了对生存的影响。中位随访20个月,1年总生存率为71.2%,1年无进展生存率为63.0%。组织学类型为乳头状癌17例,未分化癌5例,滤泡癌3例,髓样癌2例,低分化癌2例,鳞状细胞癌1例。给药后8周肿瘤缩小、分化癌、中性粒细胞-淋巴细胞比值(NLR)≤3、格拉斯哥预后评分(GPS)为0的患者无进展生存率明显提高。提示NLR和GPS可能是预测预后的新指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical analysis of lenvatinib therapy for unresectable thyroid cancer at Nagoya City University Hospital and related facilities
Lenvatinib is a molecular targeted drug indicated for unresectable radioiodine refractory thyroid cancer, but predictors of therapeutic prognosis have not been established. In this study, we retrospectively reviewed histopathological features and clinical factors in 30 cases of unresectable thyroid cancer treated with lenvatinib at Nagoya City University Hospital and related facilities, and analyzed the effects on survival. The median follow-up was 20 months, the 1-year overall survival rate was 71.2%, and the 1-year progression-free survival rate was 63.0%. The histological types were papillary carcinoma in 17 cases, undifferentiated carcinoma in 5 cases, follicular carcinoma in 3 cases, medullary carcinoma in 2 cases, poorly differentiated carcinoma in 2 cases, and squamous cell carcinoma in 1 case. The progression-free survival rate was significantly better in cases in which tumor shrinkage was observed at 8 weeks after administration, cases with differentiated carcinoma, cases in which the neutrophil-lymphocyte ratio (NLR) was ≤ 3, and cases in which the Glasgow prognostic score (GPS) was 0. It is suggested that NLR and GPS may be new predictors of prognosis.
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来源期刊
Japanese Journal of Head and Neck Cancer
Japanese Journal of Head and Neck Cancer Medicine-Otorhinolaryngology
CiteScore
0.10
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