Combined chemoimmunotherapy

  • 文章类型: Journal Article
    目的:目前正在积极开发不同的低剂量化疗方案,并将其引入临床实践。与常规化疗相比具有明显的优势(低毒性,预防耐药性),LDC还可以通过激活先天和适应性免疫的效应子并减少肿瘤相关的免疫抑制来刺激患者的抗肿瘤免疫应答。作为非清髓性的,LDC可以成功地与不同的抗癌免疫治疗策略相结合,包括免疫调节细胞因子。分泌的亲环蛋白A(CypA)在这方面是特别令人感兴趣的。以前,我们表明重组人CypA(rhCypA)具有多效免疫刺激活性和抗肿瘤作用。因此,rhCypA可能被提议作为与LDC联合治疗的透视组成部分。
    方法:在这项工作中,我们评估了rhCypA联合低剂量环磷酰胺的抗肿瘤作用,阿霉素,达卡巴嗪,和紫杉醇在小鼠黑色素瘤B16和淋巴瘤EL4的体内实验性肿瘤模型中的作用。
    结果:这些研究显示了rhCypA与LDC的协同和增强作用。此外,作为单一治疗剂和联合化学免疫疗法的组成部分,显示rhCypA通过增强巨噬细胞的肿瘤浸润来调节免疫肿瘤微环境,NK细胞,和T细胞。还发现rhCypA刺激全身和局部抗肿瘤免疫应答。
    结论:RhCypA可能被提议作为联合癌症化学免疫疗法的一个观点组成部分。
    OBJECTIVE: Different regimens of low-dose chemotherapy (LDC) are currently being actively developed and introduced into clinical practice. Along with its obvious advantages compared to conventional chemotherapy (low toxicity, prevention of drug resistance), LDC could also stimulate anti-tumor immune responses in a patient by activating effectors of innate and adaptive immunity and diminishing tumor-associated immunosuppression. As non-myeloablative, LDC could be successfully combined with different anti-cancer immunotherapeutic strategies, including immunoregulatory cytokines. Secreted cyclophilin A (CypA) is of particular interest in this respect. Previously, we showed that recombinant human CypA (rhCypA) had pleiotropic immunostimulatory activity and anti-tumor effects. Thus, rhCypA could be potentially proposed as a perspective component of combined therapy with LDC.
    METHODS: In this work, we evaluated the anti-tumor effects of rhCypA combined with low doses of cyclophosphamide, doxorubicin, dacarbazine, and paclitaxel in the experimental mouse tumor models of melanoma B16 and lymphoma EL4 in vivo.
    RESULTS: Synergic and potentiating effects of rhCypA combined with LDC were shown in these studies. Furthermore, as a monotherapeutic agent and a component of combined chemoimmunotherapy, rhCypA was shown to modulate the immune tumor microenvironment by enhancing tumor infiltration with macrophages, NK cells, and T cells. It was also found that rhCypA stimulated both systemic and local anti-tumor immune responses.
    CONCLUSIONS: RhCypA could be potentially proposed as a perspective component of the combined cancer chemoimmunotherapy.
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  • 文章类型: Journal Article
    具有阴性TTF-1表达的肺腺癌被认为是某些全身治疗的不良预后因素。然而,TTF-1表达对联合化疗免疫治疗的影响尚不清楚.我们旨在探讨晚期肺腺癌患者肿瘤TTF-1表达与联合化学免疫疗法疗效之间的关系。
    这项多中心前瞻性观察性研究纳入了日本10个机构的58例接受联合化学免疫疗法治疗的晚期肺腺癌患者。使用免疫组织化学确定TTF-1在预处理肿瘤中的表达。
    TTF-1阳性组联合化学免疫治疗的客观反应率明显高于TTF-1阴性组(p=0.02)。TTF-1阳性组的中位无进展生存期(PFS)和总生存期明显长于TTF-1阴性组(10.9对5.0个月;p=0.01)。多因素分析显示TTF-1表达是影响PFS的独立预后因素。此外,肺腺癌患者的TTF-1表达与程序性死亡配体1表达显着相关(p=0.003)。程序性死亡配体1肿瘤比例得分大于或等于50%的TTF-1阳性组的PFS明显长于其他组(p=0.02)。
    TTF-1阳性与接受联合化学免疫疗法治疗的晚期肺腺癌患者更好的临床预后相关。
    UNASSIGNED: Lung adenocarcinoma with negative TTF-1 expression is believed to be a poor prognostic factor for certain systemic treatments. Nevertheless, the impact of TTF-1 expression on combined chemoimmunotherapy remains unclear. We aimed to investigate the relationship between tumor TTF-1 expression and the efficacy of combined chemoimmunotherapy in patients with advanced lung adenocarcinoma.
    UNASSIGNED: This multicenter prospective observational study included 58 patients with advanced lung adenocarcinoma treated with combined chemoimmunotherapy across 10 institutions in Japan. The expression of TTF-1 in pretreatment tumors was determined using immunohistochemistry.
    UNASSIGNED: The objective response rate of combined chemoimmunotherapy was significantly higher in TTF-1-positive groups than in TTF-1-negative groups (p = 0.02). The median progression-free survival (PFS) and overall survival were significantly longer in TTF-1-positive groups than in TTF-1-negative groups (10.9 versus 5.0 mo; p = 0.01). Multivariate analysis revealed that TTF-1 expression was an independent favorable prognostic factor for PFS. Moreover, TTF-1 expression in patients with lung adenocarcinoma is significantly associated with programmed death-ligand 1 expression (p = 0.003). The TTF-1-positive group with programmed death-ligand 1 tumor proportion score greater than or equal to 50% had a significantly longer PFS than the other groups (p = 0.02).
    UNASSIGNED: TTF-1 positivity is associated with better clinical outcomes in patients with advanced lung adenocarcinoma treated with combined chemoimmunotherapy.
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  • 文章类型: Journal Article
    心包积液是晚期肺癌的常见表现。心包腔内存在恶性细胞或渗出液引流可引起呼吸困难症状,胸膜炎性胸痛,和晕厥。除了医生在检测和诊断恶性心包积液方面面临的困难外,考虑到患者的癌症预后和心血管稳定性,治疗可能具有挑战性。尽管恶性心包积液有多种治疗方法,包括化疗和手术,肺癌患者历来预后较差。除了肺腺癌伴恶性心包积液,该病例并发COVID-19和恶性肿瘤相关的阻塞性肺炎.我们介绍了一例64岁的晚期非小细胞肺癌(NSCLC)伴恶性心包积液的女性,尽管COVID-19检测呈阳性并患有阻塞性肺炎,在联合化学免疫疗法的全身治疗后,有良好的结局。
    Pericardial effusion is a common finding in advanced-stage lung cancer. The presence of malignant cells or drainage of exudate effusion in the pericardial space may cause symptoms of dyspnea, pleuritic chest pain, and syncope. In addition to the difficulty physicians face in the detection and diagnosis of malignant pericardial effusion, treatment may be challenging considering the cancer prognosis and cardiovascular stability of the patient. Despite the availability of several treatment modalities for malignant pericardial effusion, including chemotherapy and surgery, patients with lung cancer historically present with poor prognoses. In addition to lung adenocarcinoma with malignant pericardial effusion, this case was complicated by COVID-19 and malignancy-associated obstructive pneumonia. We present a case of a 64-year-old woman with advanced non-small cell lung carcinoma (NSCLC) with malignant pericardial effusion who, despite testing positive for COVID-19 and having obstructive pneumonia, had favorable outcomes following systemic therapy with combined chemo-immunotherapy.
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