Toshida Katsuya, Itoh Shinji, Tomiyama Takahiro, Morinaga Akinari, Kosai Yukiko, Tomino Takahiro, Kurihara Takeshi, Nagao Yoshihiro, Morita Kazutoyo, Harada Noboru, Yoshizumi Tomoharu
Department of Surgery and Science, Graduate School of Medical Sciences Kyushu University Fukuoka Japan.
JGH Open. 2022 Jun 8;6(7):477-486. doi: 10.1002/jgh3.12777. eCollection 2022 Jul.
Sarcopenia has received much attention as a poor prognostic factor in various fields, and has also been reported to worsen prognosis in patients with hepatocellular carcinoma (HCC) treated with sorafenib or lenvatinib (LEN). Atezolizumab/bevacizumab (ATZ/BEV) is recommended as first-line drug therapy for unresectable-HCC, but the effect of sarcopenia on patients treated with ATZ/BEV is unknown.
We enrolled 98 patients treated with ATZ/BEV or LEN. Computed tomography performed before the initiation of drug therapy was used to diagnose sarcopenia in accordance with the criteria proposed by the Japanese Society of Hepatology. Patients were divided into two groups based on the presence or absence of sarcopenia in each regimen, and patient characteristics, adverse events, and prognosis were compared.
In ATZ/BEV therapy, 57.1% of patients had sarcopenia. The sarcopenia group had significantly more women ( = 0.0125) and more macroscopic vascular invasion ( = 0.0270). Sarcopenia had no significant effect on progression-free survival (PFS) and overall survival (OS). In LEN therapy, 63.4% of patients had sarcopenia. The sarcopenia group was significantly older ( = 0.0064) and had a higher number of women ( = 0.0003), a higher neutrophil-lymphocyte ratio ( = 0.0222), worse albumin-bilirubin grade ( = 0.0087), and worse best response ( = 0.0255). PFS ( = 0.0091) and OS ( = 0.0006) were worse in the sarcopenia group. In multivariate analysis, age ( = 0.0362), lymphocyte-monocyte ratio ( = 0.0365), and sarcopenia ( = 0.0268) were independent prognostic factors for OS.
In ATZ/BEV therapy, sarcopenia does not determine prognosis, and therapeutic efficacy can be expected even in cases of sarcopenia.
肌肉减少症作为各领域预后不良的因素已受到广泛关注,据报道,其也会使接受索拉非尼或仑伐替尼(LEN)治疗的肝细胞癌(HCC)患者的预后恶化。阿替利珠单抗/贝伐单抗(ATZ/BEV)被推荐为不可切除HCC的一线药物治疗,但肌肉减少症对接受ATZ/BEV治疗患者的影响尚不清楚。
我们纳入了98例接受ATZ/BEV或LEN治疗的患者。根据日本肝病学会提出的标准,使用药物治疗开始前进行的计算机断层扫描来诊断肌肉减少症。根据每种治疗方案中是否存在肌肉减少症将患者分为两组,并比较患者特征、不良事件和预后。
在ATZ/BEV治疗中,57.1%的患者存在肌肉减少症。肌肉减少症组女性明显更多(P = 0.0125),肉眼可见血管侵犯更多(P = 0.0270)。肌肉减少症对无进展生存期(PFS)和总生存期(OS)无显著影响。在LEN治疗中,63.4%的患者存在肌肉减少症。肌肉减少症组年龄明显更大(P = 0.0064),女性数量更多(P = 0.0003),中性粒细胞与淋巴细胞比值更高(P = 0.0222),白蛋白-胆红素分级更差(P = 0.0087),最佳反应更差(P = 0.0255)。肌肉减少症组的PFS(P = 0.0091)和OS(P = 0.0006)更差。在多变量分析中,年龄(P = 0.0362)、淋巴细胞与单核细胞比值(P = 0.0365)和肌肉减少症(P = 0.0268)是OS的独立预后因素。
在ATZ/BEV治疗中,肌肉减少症不决定预后,即使存在肌肉减少症的病例也可预期治疗效果。