Feeney Laura, Jain Yatin, Beasley Matthew, Donnelly Oliver, Kong Anthony, Moleron Rafael, Nallathambi Chandran, Rolles Martin, Sanghera Paul, Tin Aung, Ulahannan Danny, Walter Harriet S, Webster Richard, Metcalf Robert
Department of Medical Oncology, The Christie NHS Foundation Trust, Manchester M20 4BX, UK.
Department of Oncology, University Hospitals Bristol NHS Foundation Trust, Bristol BS1 3NU, UK.
Cancers (Basel). 2021 Aug 27;13(17):4336. doi: 10.3390/cancers13174336.
Adenoid cystic carcinoma (ACC) is a rare cancer of secretory glands. Recurrent or metastatic (R/M) ACC is generally considered resistant to cytotoxic chemotherapy. Recent phase II studies have reported improved objective response rates (ORR) with the use of the multi-kinase inhibitor lenvatinib. We sought to evaluate real-world experience of R/M ACC patients treated with lenvatinib monotherapy within the UK National Health Service (NHS) to determine the response rates by Response Evaluation Criteria of Solid Tumour (RECIST) and clinical outcomes. Twenty-three R/M ACC patients from eleven cancer centres were included. All treatment assessments for clinical decision making related to drug therapy were undertaken at the local oncology centre. Central radiology review was performed by an independent clinical trial radiologist and blinded to the clinical decision making. In contrast to previously reported ORR of 12-15%, complete or partial response was not observed in any patients. Eleven patients (52.4%) had stable disease and 5 patients (23.8%) had progression of disease as the best overall response. The median time on treatment was 4 months and the median survival from discontinuation was 1 month. The median PFS and OS from treatment initiation were 4.5 months and 12 months respectively. Multicentre collaborative studies such as this are required to evaluate rare cancers with no recommended standard of care therapy and variable disease courses.
腺样囊性癌(ACC)是一种罕见的分泌腺癌症。复发性或转移性(R/M)ACC通常被认为对细胞毒性化疗耐药。近期的II期研究报告称,使用多激酶抑制剂乐伐替尼可提高客观缓解率(ORR)。我们试图评估在英国国家医疗服务体系(NHS)中接受乐伐替尼单药治疗的R/M ACC患者的真实世界经验,以根据实体瘤疗效评价标准(RECIST)确定缓解率和临床结局。纳入了来自11个癌症中心的23例R/M ACC患者。所有与药物治疗相关的临床决策的治疗评估均在当地肿瘤中心进行。由一名独立的临床试验放射科医生进行中心影像学审查,且对临床决策不知情。与先前报道的12%-15%的ORR不同,未观察到任何患者出现完全或部分缓解。11例患者(52.4%)病情稳定,5例患者(23.8%)病情进展为最佳总体缓解。中位治疗时间为4个月,停药后的中位生存期为1个月。从治疗开始计算的中位无进展生存期(PFS)和总生存期(OS)分别为4.5个月和12个月。需要开展这样的多中心协作研究来评估没有推荐标准治疗方案且疾病病程多变的罕见癌症。