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低剂量地西他滨预处理化疗免疫治疗耐药复发/难治性消化道癌患者的安全性和有效性的 Ib/II 期研究。

Phase Ib/II study of safety and efficacy of low-dose decitabine-primed chemoimmunotherapy in patients with drug-resistant relapsed/refractory alimentary tract cancer.

机构信息

Department of Molecular Biology and Bio-therapeutic, Institute of Basic Medicine, Chinese PLA General Hospital, Beijing, People's Republic of China.

Department of Surgery, Johns Hopkins University, Baltimore, MD.

出版信息

Int J Cancer. 2018 Sep 15;143(6):1530-1540. doi: 10.1002/ijc.31531. Epub 2018 Apr 26.

Abstract

The pressing need for improved therapeutic outcomes provides a good rationale for identifying effective strategies for alimentary tract (AT) cancer treatment. The potential re-sensitivity property to chemo- and immunotherapy of low-dose decitabine has been evident both preclinically and in previous phase I trials. We conducted a phase Ib/II trial evaluating low-dose decitabine-primed chemoimmunotherapy in patients with drug-resistant relapsed/refractory (R/R) esophageal, gastric or colorectal cancers. Forty-five patients received either the 5-day decitabine treatment with subsequent readministration of the previously resistant chemotherapy (decitabine-primed chemotherapy, D-C cohort) or the aforementioned regimen followed by cytokine-induced killer cells therapy (D-C and cytokine-induced killer [CIK] cell treatment, D-C + CIK cohort) based on their treatment history. Grade 3 to 4 adverse events (AEs) were reported in 11 (24.4%) of 45 patients. All AEs were controllable, and no patient experienced a treatment-related death. The objective response rate (ORR) and disease control rate (DCR) were 24.44% and 82.22%, respectively, including two patients who achieved durable complete responses. Clinical response could be associated with treatment-free interval and initial surgical resection history. ORR and DCR reached 28% and 92%, respectively, in the D-C + CIK cohort. Consistently, the progression-free survival (PFS) of the D-C + CIK cohort compared favorably to the best PFS of the pre-resistant unprimed therapy (p = 0.0001). The toxicity and ORRs exhibited were non-significantly different between cancer types and treatment cohort. The safety and efficacy of decitabine-primed re-sensitization to chemoimmunotherapy is attractive and promising. These data warrant further large-scale evaluation of drug-resistant R/R AT cancer patients with advanced stage disease.

摘要

提高治疗效果的迫切需求为确定治疗消化道(AT)癌症的有效策略提供了很好的理由。低剂量地西他滨对化疗和免疫治疗的潜在再敏感性在临床前和以前的 I 期试验中都得到了证实。我们进行了一项 Ib/II 期试验,评估了低剂量地西他滨预处理的化疗免疫治疗在耐药复发/难治性(R/R)食管、胃或结直肠癌患者中的应用。根据治疗史,45 名患者接受了 5 天的地西他滨治疗,随后重新给予以前耐药的化疗(地西他滨预处理化疗,D-C 队列),或接受上述方案,随后给予细胞因子诱导的杀伤细胞治疗(D-C 和细胞因子诱导的杀伤 [CIK] 细胞治疗,D-C+CIK 队列)。45 名患者中有 11 名(24.4%)报告了 3 级至 4 级不良事件(AE)。所有 AE 均可控制,无患者发生与治疗相关的死亡。客观缓解率(ORR)和疾病控制率(DCR)分别为 24.44%和 82.22%,包括 2 名患者获得持久完全缓解。临床反应与无治疗间隔和初始手术切除史有关。D-C+CIK 队列的 ORR 和 DCR 分别达到 28%和 92%。同样,D-C+CIK 队列的无进展生存期(PFS)明显优于未预处理的耐药前最佳 PFS(p=0.0001)。D-C+CIK 队列的毒性和 ORR 在不同癌症类型和治疗队列之间无显著差异。地西他滨预处理再致敏化疗免疫治疗的安全性和有效性具有吸引力和前景。这些数据为进一步评估晚期耐药 R/R AT 癌症患者提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4388/6099263/65086f6262b4/IJC-143-1530-g001.jpg

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