Ishikawa Toru, Terai Nanako, Sato Ryo, Natsui Hiroki, Iwasawa Takahiro, Ogawa Masahiro, Kobayashi Yuji, Sato Toshifumi, Yokoyama Junji, Iiduka Akihiko, Honma Terasu
Department of Gastroenterology, Saiseikai Niigata Hospital, Niigata, Japan;
Department of Radiology, Saiseikai Niigata Hospital, Niigata, Japan.
In Vivo. 2025 Mar-Apr;39(2):936-941. doi: 10.21873/invivo.13898.
BACKGROUND/AIM: The combination of atezolizumab and bevacizumab is the standard treatment for hepatocellular carcinoma (HCC). However, cases of portal hypertension (PHT) have been reported with atezolizumab/bevacizumab combination therapy. Splenomegaly caused by PHT may disrupt the immune environment and increase the risk of therapeutic failure with this combination therapy. Partial splenic embolization (PSE) is a treatment option for splenomegaly; however, the usefulness of PSE for PHT during atezolizumab/bevacizumab combination therapy is unclear. This study investigated the effect of PSE on the immune environment in a patient with splenomegaly caused by exacerbation of PHT during atezolizumab/bevacizumab combination therapy for HCC.
Of the 56 patients with unresectable HCC treated with atezolizumab/bevacizumab, four with splenomegaly and progressive disease (PD) underwent PSE.
PHT during atezolizumab/bevacizumab combination therapy led to a mean enlargement of the splenic size of 142.7%, an increase in the neutrophil-lymphocyte ratio (NLR), a decrease in lymphocyte counts, and a decrease in platelet counts. PSE increased platelet counts and lymphocyte counts, and decreased the NLR compared with pre-PSE levels. Atezolizumab/bevacizumab combination therapy, which caused PD due to PHT, resulted in a non-PD state with continued treatment after PSE.
In patients with PHT receiving atezolizumab/bevacizumab combination therapy, PSE promotes recovery from leukopenia and thrombocytopenia. Furthermore, PSE treatment may also induce host immune activation and boost immunity.
背景/目的:阿替利珠单抗和贝伐单抗联合用药是肝细胞癌(HCC)的标准治疗方案。然而,已有使用阿替利珠单抗/贝伐单抗联合疗法导致门静脉高压(PHT)的病例报道。PHT引起的脾肿大可能会破坏免疫环境,并增加这种联合疗法治疗失败的风险。部分脾栓塞术(PSE)是治疗脾肿大的一种选择;然而,PSE在阿替利珠单抗/贝伐单抗联合治疗期间对PHT的有效性尚不清楚。本研究调查了PSE对一名在阿替利珠单抗/贝伐单抗联合治疗HCC期间因PHT加重导致脾肿大患者免疫环境的影响。
在56例接受阿替利珠单抗/贝伐单抗治疗的不可切除HCC患者中,4例伴有脾肿大和疾病进展(PD)的患者接受了PSE。
阿替利珠单抗/贝伐单抗联合治疗期间的PHT导致脾脏平均大小增大142.7%,中性粒细胞与淋巴细胞比值(NLR)升高,淋巴细胞计数减少,血小板计数减少。与PSE前水平相比,PSE使血小板计数和淋巴细胞计数增加,NLR降低。因PHT导致PD的阿替利珠单抗/贝伐单抗联合治疗在PSE后继续治疗,结果进入非PD状态。
在接受阿替利珠单抗/贝伐单抗联合治疗的PHT患者中,PSE可促进白细胞减少和血小板减少的恢复。此外,PSE治疗还可能诱导宿主免疫激活并增强免疫力。