作者
Yusuke Ozeki,Naoya Kanogawa,Sadahisa Ogasawara,Keita Ogawa,Takamasa Ishino,Miyuki Nakagawa,Kisako Fujiwara,Hidemi Unozawa,T. Iwanaga,Takafumi Sakuma,Naoto Fujita,Ryuta Kojima,Hiroaki Kanzaki,Keisuke Koroki,Kazufumi Kobayashi,Masato Nakamura,Soichiro Kiyono,Takayuki Kondo,Tomoko Saito,Ryo Nakagawa,Eiichiro Suzuki,Yoshihiko Ooka,Shingo Nakamoto,Ryosuke Muroyama,Akinobu Tawada,Tetsuhiro Chiba,Makoto Arai,Jun Kato,Jun‐ichiro Ikeda,Yuichi Takiguchi,Naoya Kato
摘要
BackgroundWith the evolution of personalized medicine in the field of oncology, which includes optimal treatment selection using next-generation sequencing-based companion diagnostic systems and tumor-agnostic treatments according to common biomarkers, a liver tumor biopsy technique that can obtain a sufficient specimen volume must be established. The current study aimed to evaluate the safety and availability of a liver tumor biopsy technique with multiple puncture sites made using a coaxial introducer needle and embolization with gelatin sponge particles.MethodsPatients with primary or metastatic liver cancer who underwent liver tumor biopsies with puncture tract embolization using gelatin sponge (Spongel®) from October 2019 to September 2020 were included in the study. The complication and diagnostic rates were evaluated, and whether the specimen volume was sufficient for Foundation® CDx was investigated.ResultsIn total, 96 patients were enrolled in this analysis. The median total number of puncture times per patient was 3 (range 1–8). The pathological diagnostic rate was 79.2%. Using the FoundationOne® CDx, specimens with a sufficient volume required for genomic medicine were collected in 84.9% of patients. The incidence rate of bleeding was 4.2% (n = 4), and only one patient presented with major bleeding requiring transfusion.ConclusionsLiver biopsy with puncture tract embolization using a gelatin sponge may be safe and effective for collecting specimens with a volume sufficient for modern cancer treatments.