Phase II study of carboplatin–paclitaxel alone or with bevacizumab in advanced sarcomatoid carcinoma of the lung: HOT1201/NEJ024

医学 贝伐单抗 卡铂 肉瘤样癌 内科学 肺癌 化疗 肿瘤科 紫杉醇 外科肿瘤学 顺铂
作者
Satoshi Oizumi,Kei Takamura,Toshiyuki Harada,Motoko Tachihara,Naoto Morikawa,Ryoichi Honda,Satoshi Watanabe,Tetsuhiko Asao,Mamoru Kunisaki,Tatsuro Fukuhara,Rintaro Noro,Eiki Kikuchi,Yasuhiro Tsutani,Toshiyuki Tenma,Kunihiko Kobayashi,Hirotoshi Dosaka‐Akita
出处
期刊:International Journal of Clinical Oncology [Springer Science+Business Media]
卷期号:27 (4): 676-683 被引量:9
标识
DOI:10.1007/s10147-021-02113-5
摘要

ObjectivesOnly a few prospective studies have been conducted to examine the efficacy and safety of systemic chemotherapy for patients with pulmonary sarcomatoid carcinomas (PSCs). There is, thus, a crucial need to develop novel treatment strategies for this rare tumor.Patients and methodsChemotherapy-naïve patients with histologically confirmed PSCs were assigned to receive either carboplatin/paclitaxel alone (CP) or with bevacizumab (CPB) followed by bevacizumab maintenance. The primary endpoint was overall response rate (ORR). Secondary endpoints included overall survival (OS), progression-free survival (PFS), and safety.ResultsThis study was closed before accumulating the expected number of cases due to slow patient accrual. Eventually, 16 patients were enrolled. The ORR was 25.0% and disease control rate was 56.3%. CPB was administered in all four patients with an objective response [partial response (PR)]; among the four PR cases, two patients had pleomorphic carcinoma, and two had carcinosarcoma. Median PFS and median survival time (MST) in all the enrolled patients were 2.6 months and 8.8 months, respectively. Median PFS was 1.2 months in the CP group and 4.2 months in the CPB group. In addition, MST was 7.9 months in the CP group and 11.2 months in the CPB group. Hematological and non-hematological adverse events were common and reversible, although ileus (grade 4) and nasal bleeding (grade 3) occurred in one case each in the CPB group.ConclusionsCPB might be effective as first-line treatment for PSCs. Further study is warranted to clarify the role of cytotoxic chemotherapy for this rare and aggressive tumor.Clinical trials registrationUniversity Hospital Medical Information Network (UMIN) Clinical Trial Registry (UMIN000008707).
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