下一代基于抗体的癌症治疗:抗体-药物偶联物和双特异性抗体在血液系统恶性肿瘤和实体瘤中的应用
Next-generation antibody-based therapeutics in cancer: antibody-drug conjugates bispecific antibodies across hematologic malignancies and solid tumors
肿瘤学的治疗范式正在经历由抗体药物偶联物(ADC)和双特异性抗体(bsAb)驱动的深刻变革。
英文原题:Comparative study of the tumor-infiltrating lymphocytes before and after neoadjuvant chemoimmunotherapy in esophageal squamous cell carcinoma.
对于接受新辅助化免治疗的ESCC患者,达到pCR的患者具有更活跃的免疫反应,且不依赖于治疗前PD-L1表达水平,治疗前CD4 + TILs比例可能是其生存的预测因素之一。
目的:探讨食管鳞状细胞癌(ESCC)患者新辅助化疗免疫治疗前后TIL(肿瘤浸润淋巴细胞)的变化及其与疗效的关系。
本研究收集了2019年11月至2022年6月期间在我院接受新辅助化疗免疫治疗的25例ESCC患者的临床数据。新辅助治疗完成后,行Mckeown MIE手术。收集治疗前和治疗后的病理标本。进行免疫组化分析,以获得治疗前后肿瘤的TIL(肿瘤浸润淋巴细胞)(TILs)浸润情况。
7例(28%)患者达到病理完全缓解(pCR组),18例(72%)患者未达到pCR(non-pCR组)。与non-pCR组相比,pCR组治疗后CD4 + TILs比例(P = 0.012)和CD8 + TILs比例(P = 0.018)显著升高;CD20 + TILs比例无显著变化(Z = -1.933,P = 0.053)。在pCR组中,治疗后CD4 + TILs比例(P = 0.047)和CD8 + TILs比例(P = 0.036)显著升高;CD20 + TILs比例(P = 0.111)无显著变化。在non-pCR组中,治疗前后CD4 + TILs比例(P = 0.729)、CD8 + TILs比例(P = 0.712)和CD20 + TILs比例(P = 0.811)均未观察到显著变化。
BACKGROUND: OBJECTIVE: To explore changes of tumor-infiltrating lymphocytes and the relationship with therapeutic effect before and after neoadjuvant chemoimmunotherapy in patients with esophageal squamous cell carcinoma(ESCC). METHOD: This study collected clinical data from 25 ESCC patients with neoadjuvant chemoimmunotherapy from November 2019 to June 2022 in our hospital. After the completion of the neoadjuvant treatment, Mckeown MIE surgery was performed. The pathological specimen before therapy and after surgery was collected. Immunohistochemical analysis was performed to obtain the tumor-infiltrating lymphocytes (TILs) infiltration of the tumor before and after treatment. RESULT: Seven (28%) patients achieved pathology complete response (pCR group) and 18 (72%) patients did not achieve pCR (non-pCR group). Compared with non-pCR group, the after treatment proportion of CD4 + TILs (P = 0.012) and the proportion of CD8 + TILs (P = 0.018) were significantly increased in pCR group; There was no significant change in the proportion of CD20 + TILs (Z = -1.933, P = 0.053). In pCR group, the proportion of CD4 + TILs (P = 0.047) and the proportion of CD8 + TILs (P = 0.036) were significantly increased after treatment; The proportion of CD20 + TILs (P = 0.111) did not change significantly. In non-pCR group, no significant changes were observed in proportions of CD4 + TILs (P = 0.729), CD8 + TILs (P = 0.712), and CD20 + TILs (P = 0.811) between before and after treatment. CONCLUSION: For ESCC patients who received neoadjuvant chemoimmunotherapy, patients with pCR had a more active immune response independent of pre-treatment PD-L1 expression levels, and the pre-treatment CD4 + TILs ratio may be one of the predictors of their survival.
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