决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Human Epidermal Growth Factor Receptor 2 Positive Advanced Gastric or Esophagogastric Adenocarcinoma: Reflecting on the Past to Gain a New Insights.
Human Epidermal Growth Factor Receptor 2 Positive Advanced Gastric or Esophagogastric Adenocarcinoma: Reflecting on the Past to Gain a New Insights.
曲妥珠单抗作为 HER2 阳性 AGC 的标准治疗已长达十年,随后,抗体偶联药物(ADC)德曲妥珠单抗问世,并展现出令人瞩目的缓解。
综述目的:人表皮生长因子受体2(HER2)是晚期胃癌(AGC)的关键靶点。本文综述HER2阳性AGC的当前治疗格局、既往临床试验的经验教训以及未来治疗策略前景。 近期发现:曲妥珠单抗曾是HER2阳性AGC的标准治疗长达十年,之后抗体药物偶联物曲妥珠单抗德鲁替康显示出显著应答。近期,一线化疗联合曲妥珠单抗加用帕博利珠单抗已成为新的标准治疗。既往针对HER2的疗法在HER2阳性乳腺癌中成功、但在AGC中失败的临床试验,加深了我们对耐药机制的理解。基于这些结果,多项新型HER2靶向疗法临床试验正在开展,包括CAR-T细胞和疫苗等免疫学策略。循环肿瘤DNA也有望用于实时生物标志物分析。此外,具有旁观者效应的抗体药物偶联物可能将HER2靶向治疗拓展至HER2表达肿瘤,包括HER2低表达AGC。吸取既往试验经验后,新型HER2靶向疗法正持续发展,适用范围也拓展至HER2表达型AGC。同时,对于HER2低表达AGC且同时具有CLDN18.2等其他生物标志物的病例,如何选择最佳治疗仍然具有挑战。
PURPOSE OF REVIEW: Human epidermal growth factor receptor 2 (HER2) is a critical target in advanced gastric cancer (AGC). This review highlights the current treatment landscape, lessons learned from past clinical trials, and prospects for future treatment strategies for HER2-positive AGC. RECENT FINDINGS: Trastuzumab had been the standard treatment for HER2-positive AGC for a decade, and subsequently, trastuzumab deruxtecan, an antibody-drug conjugate (ADC), emerged with an impressive response. Recently, the addition of pembrolizumab to first-line chemotherapy plus trastuzumab has become a novel standard treatment. Past clinical trials of HER2-targeted therapies, which succeeded in HER2-positive breast cancer but failed in AGC, have deepened our understanding of resistance mechanisms. Based on these results, several clinical trials of novel HER2-targeted therapies, including immunologic approaches such as CAR-T cells and vaccines, are currently ongoing. Circulating tumor DNA is also expected to be a tool for real-time biomarker analysis. Additionally, ADCs with a bystander effect have the potential to expand the scope of HER2-targeted therapies to HER2-expressing, including HER2-low AGC. Learning from past trials, further development of novel HER2-targeted therapies is underway, expanding their scope to HER2-expressing AGC. Meanwhile, selecting optimal treatment is a challenging issue in cases with HER2-low AGC overlapping with other biomarkers like CLDN18.2.
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