彭布罗利珠单抗
医学
放化疗
多西紫杉醇
甲状腺间变性癌
放射治疗
队列
中期分析
肿瘤科
内科学
癌症
临床终点
外科
甲状腺癌
临床试验
免疫疗法
作者
Ashish V. Chintakuntlawar,Jun Yin,Robert L. Foote,Jan L. Kasperbauer,Michael Rivera,Erik Asmus,Nina I. Garces,Jeffrey R. Janus,Minetta C. Liu,J. Daniel,Eric J. Moore,John C. Morris,M.A. Neben-Wittich,Daniel L. Price,Katharine A. Price,Mabel Ryder,Kathryn M. Van Abel,Crystal Hilger,Eleyna Samb,Keith C. Bible
出处
期刊:Thyroid
[Mary Ann Liebert]
日期:2019-10-09
卷期号:29 (11): 1615-1622
被引量:61
标识
DOI:10.1089/thy.2019.0086
摘要
Background: Anaplastic thyroid cancer (ATC) has poor prognosis with median overall survival (OS) of ∼6 months. We previously reported high PD-1/PDL-1 staining in ATC, raising the possibility of the productive application of the immunotherapeutic pembrolizumab. However, having found pembrolizumab to anecdotally have limited single-agent activity in ATC, we sought to alternatively define whether pembrolizumab might synergistically combine with chemoradiotherapy as initial ATC therapy. Methods: An investigator-initiated therapeutic phase 2 trial of pembrolizumab, 200 mg intravenously (IV) every 3 weeks, combined with chemoradiotherapy (docetaxel/doxorubicin, 20 mg/m2 each IV weekly plus volumetric modulated arc therapy) was initiated as frontline therapy (with or without surgery) in ATC to assess efficacy and toxicities. Six-month OS was selected as the primary endpoint using a Simon's optimal design with interim analysis (targeting accrual of 25 patients; Cohort A: prior resection, Cohort B: no resection). Based on a prior patient cohort-treated similarly, but without pembrolizumab, the design was such that, if 6-month true survival is 75%, the probability of declaring the approach worthy of further pursuit would be 91%. Results: Three patients were enrolled, two with rapidly enlarging unresectable neck masses. Early tumor responses were favorable in all three, and all three satisfactorily completed: intended radiotherapy, preceding and radiotherapy-concurrent pembrolizumab, and concurrent chemoradiotherapy. However, all three patients died <6 months following therapy initiation-one from pulmonary metastases and two from otherwise unexpected fatal pulmonary complications occurring subsequent to chemoradiotherapy completion-prompting study closure. Conclusions: Although initially tolerated and effective in terms of locoregional disease control, disappointing survival outcomes compared with historical controls raise uncertainty that the piloted approach merits further pursuit in ATC.
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