Atezolizumab with bevacizumab, paclitaxel and carboplatin was effective for patients with SMARCA4-deficient thoracic sarcoma

被引:52
作者
Kawachi, Hayato [1 ]
Kunimasa, Kei [1 ]
Kukita, Yoji [2 ]
Nakamura, Harumi [2 ]
Honma, Keiichiro [3 ]
Kawamura, Takahisa [1 ]
Inoue, Takako [1 ]
Tamiya, Motohiro [1 ]
Kuhara, Hanako [1 ]
Nishino, Kazumi [1 ]
Mizote, Yu [4 ]
Akazawa, Takashi [4 ]
Tahara, Hideaki [4 ,5 ]
Kumagai, Toru [1 ]
机构
[1] Osaka Int Canc Inst, Dept Thorac Oncol, Osaka, Japan
[2] Osaka Int Canc Inst, Lab Genom Pathol, Osaka, Japan
[3] Osaka Int Canc Inst, Dept Diagnost Pathol Cytol, Osaka, Japan
[4] Osaka Int Canc Inst, Dept Canc Drug Discovery Dev, Osaka, Japan
[5] Univ Tokyo, Inst Med Sci, Project Div Canc Biomol Therapy, Tokyo, Japan
基金
日本学术振兴会;
关键词
atezolizumab; bevacizumab; immunotherapy; SMARCA4-DTS; SMARCA4-DTST; CELL LUNG-CANCER;
D O I
10.2217/imt-2020-0311
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
SMARCA4-deficient thoracic sarcoma (DTS) is a recently noted progressive thoracic malignancy. We recently experienced three cases of SMARCA4-DTS who were treated with atezolizumab in combination with bevacizumab, paclitaxel and carboplatin (ABCP) as the first-line therapy. Immunohistopathological analysis revealed absent expression of SMARCA4 in all cases. The tumor mutational burden was over 11/Mb and mutations in SMARCA4 and TP53 were detected in all three cases. Partial response to ABCP treatment was observed in all three cases, with a progression-free survival of approximately 6 months or longer and a continuous response of 1 year or longer in one case. The first-line ABCP treatment demonstrated durable efficacy in SMARCA4-DTS regardless of the degree of PD-L1 expression. Lay abstract Lung cancer is the leading cause of cancer-related death worldwide. Among them, SMARCA4-deficient thoracic sarcoma (DTS), which lacks SMARCA4 expression and exhibits an undifferentiated carcinoma histology, is a recently identified subtype of lung cancer. It tends to occur in younger people with heavy smoking status and has been reported to recur quickly and have a poor prognosis even after chemotherapy, radiation therapy or surgery. There is no effective molecularly targeted agent for SMARCA4-DTS and the identification of an effective therapy is required. Here, we report the clinical features and genomic information of three SMARCA4-DTS cases in which atezolizumab with bevacizumab, paclitaxel and carboplatin treatment was effective. This report suggests the efficacy of atezolizumab with bevacizumab, paclitaxel and carboplatin treatment compared with conventional chemotherapy.
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收藏
页码:799 / 806
页数:8
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