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

Author:

Kawachi Hayato1,Kunimasa Kei1ORCID,Kukita Yoji2,Nakamura Harumi2,Honma Keiichiro3,Kawamura Takahisa1,Inoue Takako1,Tamiya Motohiro1,Kuhara Hanako1,Nishino Kazumi1,Mizote Yu4,Akazawa Takashi4,Tahara Hideaki45,Kumagai Toru1

Affiliation:

1. Department of Thoracic Oncology, Osaka International Cancer Institute, Osaka, Japan

2. Laboratory of Genomic Pathology, Osaka International Cancer Institute, Osaka, Japan

3. Department of Diagnostic Pathology & Cytology, Osaka International Cancer Institute, Osaka, Japan

4. Department of Cancer Drug Discovery & Development, Osaka International Cancer Institute, Osaka, Japan

5. Project Division of Cancer Biomolecular Therapy, Institute of Medical Science, The University of Tokyo, Tokyo, Japan

Abstract

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.

Funder

Japan Society for the Promotion of Science

Takeda Science Foundation

Osaka International Cancer Institute

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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