RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Incidence and Predictive Factors of Pathological Complete Response in Rectal Cancer Patients Undergoing Neoadjuvant Chemoradiation Therapy.
Incidence and Predictive Factors of Pathological Complete Response in Rectal Cancer Patients Undergoing Neoadjuvant Chemoradiation Therapy.
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过去几十年,直肠癌的治疗结局已显著改善。对治疗相关并发症的担忧促成了诸如全程新辅助治疗和非手术治疗等细化策略。主要目的是确定在接受新辅助放化疗的局部晚期直肠癌中与病理完全缓解相关的预测因素。次要目的是估计研究人群中 pCR 和 cCR 的发生率,并确定 cCR 与 pCR 的一致率。
我们纳入了 84 例诊断为非转移性直肠癌的患者,这些患者于 2018 年 9 月至 2020 年 3 月在本机构接受了新辅助长程放化疗(CTRT)和根治性手术。收集了临床病理和治疗资料。分析了临床完全缓解(cCR)和病理完全缓解(pCR)率,并与基线和组织病理学特征进行比较。在 84 例接受 CTRT 后根治性手术的患者中,分别有 23 例(27.4%)和 16 例(19%)达到 cCR 和 pCR。完成 CTRT 的平均时间和至手术的间隔分别为 35.33 天和 57.86 天。大多数为 3 期(96.4%)、中低位直肠(95.4%)和中分化(69%)癌。尽管 cCR 是 pCR 的显著预测因素(p = .01),但 cCR 组中非 pCR 的比例为 43.5%,而非 cCR 者中有 4.9% 在术后病理标本中达到 pCR。发现治疗前 CEA 水平和中性粒细胞:淋巴细胞比值、肿瘤分化、TIL(肿瘤浸润淋巴细胞)反应与 pCR 具有统计学显著关联。在我们的人群中,cCR 和 pCR 率分别为 27.4% 和 19%。与现有文献相反,肿瘤位置、T4和N2分期不能预测pCR。由于pCR率低且cCR与pCR之间存在显著不一致,在考虑非手术治疗前,必须采用严格的筛选策略。
Treatment outcomes for rectal cancer have improved significantly over the last few decades. Concerns regarding the morbidity of treatment have led to nuances like total neoadjuvant therapy and nonoperative management. The primary objective was to determine the predictive factors associated with pathological complete response in locally advanced carcinoma rectum undergoing neoadjuvant chemoradiation. The secondary objectives were to estimate the incidence of pCR and cCR in the study population, and to determine the concordance rate of cCR with pCR.
We included 84 patients diagnosed with nonmetastatic rectal cancer who underwent neoadjuvant long-course chemoradiation (CTRT) and radical surgery during September 2018 to March 2020 at the institute. The clinicopathological and treatment details were collected. Rates of clinical (cCR) and pathological complete response (pCR) were analyzed and compared with baseline and histopathological characteristics. Of 84 patients who underwent radical surgery following CTRT, 23 (27. 4%) and 16 (19%) had cCR and pCR, respectively. Mean duration for completion of CTRT and interval to surgery were 35. 33 days and 57. 86 days, respectively. The majority were stage 3 (96. 4%), low-middle rectal (95. 4%), and moderately differentiated (69%) cancers.
Even though cCR was a significant predictor of pCR ( p = . 01), the rate of non pCR in the cCR group was 43. 5% while 4. 9% of the non cCR had pCR in the postoperative pathological specimen. Pre-treatment CEA level and neutrophil: lymphocyte ratio, differentiation of tumor, tumor infiltrating lymphocyte response were found to have a statistical significant association with pCR.
The rate of cCR and pCR was 27. 4% and 19% respectively in our population. The tumor location, T4 and N2 stages, in contrary to the existing literature, do not predict a pCR. With the low rate of pCR and significant discordance between cCR and pCR, stringent selection strategies are mandatory before contemplating a nonoperative management.
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