Abdel Ghafar Muhammad Tarek, Morad Morad Ahmed, El-Zamarany Enas A, Ziada Dina, Soliman Hanan, Abd-Elsalam Sherief, Salama Marwa
Clinical Pathology Department Faculty of Medicine, Tanta University, Egypt.
Clinical Pathology Department Faculty of Medicine, Tanta University, Egypt.
Int Immunopharmacol. 2020 Mar 10;82:106375. doi: 10.1016/j.intimp.2020.106375.
This is a randomized trial adopted to evaluate the safety and efficacy of immunization with specific anti-hepatocellular carcinoma dendritic cells (DCs) in Egyptian patients with advanced hepatocellular carcinoma (HCC) as a treatment or adjuvant therapy in comparison with the traditional therapy.
This study was conducted on 20 HCC patients who were assigned to four groups according to BCLC staging; group I: HCC patients (stage B) received trans-arterial chemoembolization (TACE) and DCs as an adjuvant therapy; group II: HCC patients (stage B) received TACE only; group III: advanced HCC patients (stage D) received DCs vaccine; group IV: advanced HCC patients (stage D) received supportive treatment. DCs were generated from peripheral blood monocytes and pulsed with a lysate of an allogeneic hepatic cancer cell line (HepG2). Toxicity and immunological response were reported as primary outcomes whereas clinical biochemical and radiological responses were reported as secondary outcomes.
Our study detected that patients who received DCs vaccine (group III) showed mild decrease in Child-Pugh score as well as AFP and PIVKA II levels and developed 20% partial response [PR] 40% stable disease [SD] and 40% progressive disease [PD] compared to the patients of group IV on supportive treatment who developed 100% PD. Although group I patients developed PR (60%) SD (20%) and PD (20%) no significant difference was detected in the clinical biochemical or radiological response between group I and group II patients. DCs vaccine had minimal adverse effects with no autoimmunity and elicited a better immunological response such as increased CD8 cells percentage and number as well as decreased TGFβ levels in the vaccinated patients.
DCs vaccine is safe as it is not associated with significant toxicity. However due to the small number of included patients the efficacy and immune response of using DCs vaccine in the treatment of advanced HCC patients need to be justified by testing of a large cohort.
本随机试验旨在评估特异性抗肝细胞癌树突状细胞(DC)免疫疗法在埃及晚期肝细胞癌(HCC)患者中作为治疗或辅助治疗与传统疗法相比的安全性和有效性。
本研究对20例HCC患者进行,根据巴塞罗那临床肝癌(BCLC)分期分为四组;第一组:HCC患者(B期)接受经动脉化疗栓塞术(TACE)并联合DC作为辅助治疗;第二组:HCC患者(B期)仅接受TACE;第三组:晚期HCC患者(D期)接受DC疫苗;第四组:晚期HCC患者(D期)接受支持治疗。DC由外周血单核细胞生成,并用同种异体肝癌细胞系(HepG2)的裂解物进行脉冲处理。毒性和免疫反应作为主要结局报告,而临床生化和放射学反应作为次要结局报告。
我们的研究发现,接受DC疫苗的患者(第三组)Child-Pugh评分以及甲胎蛋白(AFP)和异常凝血酶原(PIVKA II)水平轻度下降,与接受支持治疗的第四组患者相比,出现了20%的部分缓解(PR)、40%的疾病稳定(SD)和40%的疾病进展(PD),第四组患者疾病进展率为100%。虽然第一组患者出现了PR(60%)、SD(20%)和PD(20%),但第一组和第二组患者在临床生化或放射学反应方面未检测到显著差异。DC疫苗的不良反应极小,无自身免疫性,并且在接种疫苗的患者中引发了更好的免疫反应,如CD8细胞百分比和数量增加以及转化生长因子β(TGFβ)水平降低。
DC疫苗是安全的,因为它与显著毒性无关。然而,由于纳入患者数量较少,使用DC疫苗治疗晚期HCC患者的疗效和免疫反应需要通过大量队列研究来验证。