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Topical 5-aminolevulinic acid-mediated photodynamic therapy versus loop electrosurgical excision procedure in the treatment of cervical intraepithelial neoplasia. 局部5-氨基乙酰丙酸介导的光动力疗法与环形电切术治疗宫颈上皮内瘤变的比较。
Pub Date : 2024-01-01 Epub Date: 2024-11-28 DOI: 10.1007/s44178-024-00127-3
Yidi Liu, Yi Li, Huan Wu, Ying Wang, Jing Zeng, Hui Li, Haixia Qiu, Ying Gu

Objective: To compare effectiveness of topical 5-aminolevulinic acid-mediated photodynamic therapy (5-ALA PDT) and loop electrosurgical excision procedure (LEEP) among patients with cervical intraepithelial neoplasia (CIN).

Methods: We retrospectively identified patients who underwent either 5-ALA PDT or LEEP from Sep. 2012 to Dec. 2019 in Chinese PLA general hospital. Patients' outcomes were compared according to the HPV genotyping, cytological tests within 3-6-month follow-up post-treatment, the pathological examination would be performed if the cytological results indicated the risk of CIN. Propensity score matching (PSM) was adapted to pair the baseline. Complete remission (CR), partial remission (PR) and the remission rate of HPV infections were used to evaluate the efficacy of 5-ALA PDT versus LEEP.

Results: In total, 30 pairs were matched as the matching tolerance was set as 0.03. There was no significant difference about the CR and PR between 5-ALA PDT and LEEP group (73.33% vs 84.00%, P = 0.340; 3.33% vs 4.00%, P = 1.000). Among different CIN group, there was no statistic difference between 5-ALA PDT and LEEP. Moreover, in terms of HPV remission rate, 5-ALA PDT showed the same efficacy as LEEP (59.26% vs 53.85%, P = 0.691).

Conclusions: In essence, topical 5-ALA PDT emerges as a non-invasive, repeatable procedure with minimal side effects for cervical lesions, preserving cervical structure. Overall, the efficacy of 5-ALA PDT is comparable to LEEP in achieving successful outcomes.

目的:比较外用5-氨基乙酰丙酸介导的光动力疗法(5-ALA PDT)和环形电切术(LEEP)治疗宫颈上皮内瘤变(CIN)的疗效。方法:回顾性分析2012年9月至2019年12月在中国人民解放军总医院接受5-ALA PDT或LEEP治疗的患者。根据HPV基因分型、治疗后随访3-6个月细胞学检查比较患者结局,细胞学结果提示有CIN风险时行病理检查。采用倾向评分匹配(PSM)对基线进行配对。用HPV感染完全缓解(CR)、部分缓解(PR)和缓解率来评价5-ALA PDT与LEEP的疗效。结果:共匹配30对,匹配公差设为0.03。5-ALA PDT组与LEEP组CR、PR差异无统计学意义(73.33% vs 84.00%, P = 0.340;3.33% vs 4.00%, P = 1.000)。不同CIN组间5-ALA PDT与LEEP差异无统计学意义。在HPV缓解率方面,5-ALA PDT与LEEP的疗效相同(59.26% vs 53.85%, P = 0.691)。结论:从本质上讲,局部5-ALA PDT是一种无创、可重复的手术,对宫颈病变的副作用最小,保留了宫颈结构。总体而言,5-ALA PDT在获得成功结果方面的疗效与LEEP相当。
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引用次数: 0
Prospect of immunotherapy alone in patients with advanced NSCLC with high btmb: a review and a meta-analysis 高btmb晚期NSCLC患者单独使用免疫疗法的前景:综述与荟萃分析
Pub Date : 2023-12-21 DOI: 10.1007/s44178-023-00065-6
Feiyu Zhao, Xiaochen Qiu, Qinna Yang, Shuyue Gao, Fan Yang, Niansong Qian
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引用次数: 0
An overview of current development and barriers on liquid biopsy in patients with early-stage non-small-cell Lung cancer 概述液体活检在早期非小细胞肺癌患者中的发展现状和障碍
Pub Date : 2023-12-20 DOI: 10.1007/s44178-023-00066-5
Yichen Jin, Fan Yang, Kezhong Chen
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引用次数: 0
Role of signaling pathways in the interaction between microbial, inflammation and cancer 信号通路在微生物、炎症和癌症相互作用中的作用
Pub Date : 2023-12-01 DOI: 10.1007/s44178-023-00064-7
A. H. Nwabo Kamdje, Richard Tagne Simo, Hetvet Paulain Fogang Dongmo, Amel Renaud Bidias, Palmer Masumbe Netongo
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引用次数: 0
China Anti-Cancer Association (CACA) guidelines for holistic integrative management of lymphoma (version 2022) 中国抗癌协会(CACA)淋巴瘤整体综合治疗指南(2022 年版)
Pub Date : 2023-11-27 DOI: 10.1007/s44178-023-00063-8
Qingyuan Zhang, Jifeng Feng, Huaqing Wang, Huiqiang Huang, Huilai Zhang, Xiaoqiu Li, Yuhuan Gao, Yongping Song, Zhiming Li, Ou Bai, Junning Cao, Hui Zhou, Kangsheng Gu, Shu Zhao, Wenhui Zhao, Yan Qin, Yajun Li, Guangyu Ma, Shujuan Wen, Yu Wang, Peiqi Zhao, Wei Guo, Fangfang Lv, Yuyang Tian, Xinrui Chen, Zucheng Xie, Yuankai Shi
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引用次数: 0
Identification of leukocyte-lymphocyte ratio as a novel prognostic factor in Peripheral T-cell lymphoma 外周血t细胞淋巴瘤中白细胞-淋巴细胞比值的新预后因子鉴定
Pub Date : 2023-10-26 DOI: 10.1007/s44178-023-00062-9
Shi-Qi Gao, Bo-Ya Lei, Yue Xu, Zi-Jian Zhang, Xing-Jian Niu, Wen-Hui Zhao, Qing-Yuan Zhang, Shu Zhao
Abstract Purpose Peripheral T-cell lymphoma (PTCL) is notorious for its heterogeneity as well as poor prognosis. High mortality remains a challenge. Our study aims to assess whether the leukocyte-lymphocyte ratio (LLR) and neutrophil-lymphocyte ratio (NLR) can be applied as prognostic indexes for patients with PTCL and supplement the prognostic system of PTCL. Methods We reviewed the data of 108 newly diagnosed PTCL patients in the clinic. The χ 2 test was applied to contrast baseline characteristics between patients in different groups divided according to the cut-off value of LLR or NLR. The Kaplan-Meier method was adapted to develop the survival curve. The COX ratio risk regression model was used to identify the indexes related to patient survival. Results LLR ≥ 10.30, NLR ≥ 8.25, Eastern Cooperative Oncology Group (ECOG) score ≥ 2, International prognostic index (IPI) score > 2, Prognostic Index for T cell lymphoma (PIT) ≥ 2, B symptom, Ann Arbor stage III-IV and high level of Lactic dehydrogenase (LDH) were poor prognosis factors impacting patients’ overall survival (OS) by the univariate analysis. The multivariate analysis illustrated that only LLR ≥ 10.30 was significantly related to OS ( P all < 0.05). Conclusion Overall, our analysis revealed that LLR ≥ 10.30 was significantly associated with poorer OS and was a novel prognostic index for PTCL.
目的外周t细胞淋巴瘤(PTCL)因其异质性和预后差而臭名昭著。高死亡率仍然是一个挑战。本研究旨在探讨白细胞-淋巴细胞比值(LLR)和中性粒细胞-淋巴细胞比值(NLR)是否可以作为PTCL患者的预后指标,补充PTCL的预后体系。方法回顾性分析108例新诊断PTCL患者的临床资料。采用χ 2检验比较按LLR或NLR截断值分组的不同组患者的基线特征。采用Kaplan-Meier法绘制生存曲线。采用COX比值风险回归模型识别与患者生存相关的指标。结果LLR≥10.30,NLR≥8.25,东部肿瘤合作组(ECOG)评分≥2,国际预后指数(IPI)评分>2、单因素分析显示,T细胞淋巴瘤(PIT)预后指数≥2、B症状、Ann Arbor III-IV期及乳酸脱氢酶(LDH)水平高是影响患者总生存期(OS)的不良预后因素。多因素分析显示,只有LLR≥10.30与OS显著相关(P均<0.05)。总的来说,我们的分析显示LLR≥10.30与较差的OS显著相关,是PTCL的一个新的预后指标。
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引用次数: 0
Prognostic analysis of prostaglandin D2 synthase in diffuse large B-cell lymphoma 前列腺素D2合酶在弥漫性大b细胞淋巴瘤中的预后分析
Pub Date : 2023-10-26 DOI: 10.1007/s44178-023-00060-x
Jiesong Wang, Yun Xu, Wei Yu, Yanbin Zheng, Hongming He, Daoguang Chen, Siping Zou, Chang Wang, Ying Chen, Ningbin Chen, Hui Wu, Jianchao Wang, Jianyang Lin
Abstract Purpose We aimed to analyse the correlation between prostaglandin D2 synthase (PTGDS) and a diffuse large B-cell lymphoma (DLBCL) prognosis. Methods We retrospectively collected two hundred paraffin-embedded tissue specimens that were pathologically diagnosed as DLBCL in the Fujian Tumour Hospital between January 2014 and December 2018. An abundance of paraffin-embedded tumour tissues were obtained. Twenty patients with lymphocyte-rich, benign, tissue-reactive, hypertrophic tonsillitis were selected as controls. Wax blocks were selected for primary cases and the controls were screened by professional pathologists. The levels of prostaglandin D2 synthase (PTGDS) and the EMT-related molecules, E-cadherin and vimentin, were detected by immunohistochemistry in clinical samples. A chi-square test revealed the correlations between PTGDS expression and clinicopathological characteristics, including age, sex, primary site, clinical stage, immunotyping, and International Prognostic Index (IPI) score. The Kaplan–Meier survival analysis was performed, and the diagnostic value was evaluated by receiver operating characteristic (ROC) curve analysis. Results A total of 138 cases (69%) were found to be PTGDS positive (> 30% positive cells). PTGDS staining was negative (< 30% positive cells) in 62 cases (31%). We collected the corresponding clinicopathological information and found that PTGDS expression was not significantly related to the patients’ age, tumour stage, presence of extranodal invasion, or IPI score. According to the follow-up data, patients with low PTGDS expression had poor progression-free survival (PFS) and overall survival (OS), with 2-year PFS and OS rates of 41.7% and 50%, respectively. The 2-year PFS and OS rates of PTGDS-positive patients were 89.3% and 92.9%, respectively ( P < 0.0001), and the differences were significant. Conclusion We found that the expression level of PTGDS is significantly correlated with the prognosis of diffuse large B-cell lymphoma.
目的探讨前列腺素D2合成酶(PTGDS)与弥漫性大b细胞淋巴瘤(DLBCL)预后的关系。方法回顾性收集2014年1月至2018年12月福建省肿瘤医院病理诊断为DLBCL的石蜡包埋组织标本200例。获得了大量石蜡包埋的肿瘤组织。选取20例淋巴细胞丰富、良性、组织反应性肥厚性扁桃体炎患者作为对照。主要病例选择蜡块,对照组由专业病理学家筛选。应用免疫组化方法检测临床标本中前列腺素D2合成酶(PTGDS)及emt相关分子e -钙粘蛋白(E-cadherin)、静脉溶蛋白(vimentin)水平。卡方检验显示PTGDS表达与临床病理特征(包括年龄、性别、原发部位、临床分期、免疫分型和国际预后指数(IPI)评分)之间存在相关性。进行Kaplan-Meier生存分析,并通过受试者工作特征(ROC)曲线分析评估诊断价值。结果138例(69%)PTGDS阳性(>30%阳性细胞)。PTGDS染色为阴性(<阳性细胞占30%)62例(31%)。我们收集了相应的临床病理资料,发现PTGDS的表达与患者的年龄、肿瘤分期、有无结外浸润或IPI评分无显著相关性。随访数据显示,PTGDS低表达患者的无进展生存期(PFS)和总生存期(OS)较差,2年PFS和OS率分别为41.7%和50%。ptgds阳性患者的2年PFS和OS率分别为89.3%和92.9% (P <0.0001),差异有统计学意义。结论PTGDS的表达水平与弥漫性大b细胞淋巴瘤的预后有显著相关性。
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引用次数: 0
Recent highlights of cancer immunotherapy 癌症免疫治疗的最新进展
Pub Date : 2023-10-20 DOI: 10.1007/s44178-023-00057-6
Xianqun Fan
Abstract Cancer immunotherapy represents a groundbreaking paradigm shift in the field of cancer treatment, harnessing the power of the immune system to combat cancer cells. As an innovative approach, it has shown immense promise and has revolutionized the way we perceive and treat cancer. This commentary aims to highlight the recent important advances in cancer immunotherapy, including immune checkpoint blockade therapy, chimeric antigen receptor T cell therapy, T cell receptor-gene engineered T cell therapy, and tumor vaccines.
癌症免疫疗法代表了癌症治疗领域的突破性范式转变,利用免疫系统的力量来对抗癌细胞。作为一种创新的方法,它已经显示出巨大的希望,并彻底改变了我们认识和治疗癌症的方式。本评论旨在强调癌症免疫治疗的最新重要进展,包括免疫检查点阻断治疗、嵌合抗原受体T细胞治疗、T细胞受体基因工程T细胞治疗和肿瘤疫苗。
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引用次数: 0
Hepatitis B virus–associated diffuse large B cell lymphoma: epidemiology, biology, clinical features and HBV reactivation 乙型肝炎病毒相关弥漫性大B细胞淋巴瘤:流行病学、生物学、临床特征和HBV再激活
Pub Date : 2023-10-20 DOI: 10.1007/s44178-023-00061-w
Zhu Jiayu, Qingyuan Zhang
Abstract Diffuse large B cell lymphoma (DLBCL) is the most common type of lymphoma in adults with high heterogeneity. Recent studies have manifested that the occurrence and development of DLBCL is related to hepatitis B virus (HBV) infection. As a medium-to-high prevalence area of HBV infection in China, the importance and exact mechanism of HBV infection in the occurrence of DLBCL have attracted considerable attention. HBV-associated DLBCL has unique clinical characteristics, poor treatment effect and inferior prognosis. HBV reactivation caused by DLBCL treatment also needs for constant vigilance. In this review we summarize the current research progress in the epidemiology, pathogenesis, clinical characteristics, HBV reactivation and antiviral therapies of HBV-associated DLBCL, in order to provide reference for clinical diagnosis and treatment.
弥漫性大B细胞淋巴瘤(DLBCL)是成人中最常见的淋巴瘤类型,具有高度异质性。近年来研究表明,DLBCL的发生发展与乙型肝炎病毒(HBV)感染有关。中国作为HBV感染的中高流行区,HBV感染在DLBCL发生中的重要性和确切机制备受关注。hbv相关DLBCL临床特点独特,治疗效果差,预后差。DLBCL治疗引起的HBV再活化也需要时刻警惕。现就HBV相关DLBCL的流行病学、发病机制、临床特点、HBV再激活及抗病毒治疗等方面的研究进展进行综述,以期为临床诊断和治疗提供参考。
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引用次数: 0
Immunochemotherapy combined with novel agents for Richter syndrome: report of 3 cases 免疫化疗联合新型药物治疗Richter综合征3例报告
Pub Date : 2023-10-17 DOI: 10.1007/s44178-023-00059-4
Lijie Xing, Hui Wang, Dan Liu, Qiang He, Zengjun Li
Abstract Objective Richter syndrome (RS) occurs in approximately 2–10% of chronic lymphocytic leukemia (CLL) patients, more often during the disease course than at diagnosis, with a diffuse large B-cell Lymphoma (DLBCL) histology in 95% of cases. Despite great advances in the treatment of CLL in recent years, RS also develops in patients treated with novel agents, as summarized in our case report and review. Methods We summarized 3 patients with RS treated with immunochemotherapy combined with BTK inhibitor (BTKi) or BCL2 inhibitor (BCL2i) and reviewed the literature. Results Three RS patients were summarized. Patient 1 was transformed into DLBCL during dose reductions in ibrutinib and achieved bone marrow (BM) minimal residual disease (MRD)-negative complete response (CR) after rituximab etoposide, dexamethasone, doxorubicin, cyclophosphamide, and vincristine (R-EDOCH) combined with BTKi treatment and sustained progression-free survival (PFS) for more than 2 years. Patient 2, who transformed at the time of diagnosis, progressed after being treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP), followed by PD1 antibody combined with cytosine, arabinoside, cisplatin and dexamethasone (DHAP) treatment and PD1 antibody combined with ifosfamide, carboplatin, and etoposide (ICE) treatment. Patient 2 achieved CR after treatment with rituximab, gemcitabine, and oxaliplatin (R-GemOx) combined with BTKi. Patient 3, who transformed at the time of diagnosis with CARD11, TP53, and ATM mutations, progressed after being treated with R-EDOCH combined with BTKi and achieved MRD-negative CR after treatment with R-GemOx and venetoclax, which has continued for 3 months. We summarized new protocols utilizing targeted therapy, such as BTKi acalabrutinib, and checkpoint inhibition, and the potential role of precision medicine in future trials of RS treatment. The efficacy of these protocols as single agents or in combination with immunochemotherapy is currently being evaluated. Conclusion In our study, immunochemotherapy combined with BTKi or BCL2i achieved favorable efficacy in the treatment of RS. The treatments should be optimized by the combination of both chemotherapies and targeted therapy to develop a specific individual approach for each patient, according to previous treatment and biological characteristics.
【摘要】目的Richter综合征(RS)发生在约2-10%的慢性淋巴细胞白血病(CLL)患者中,在病程中比在诊断时更常见,95%的病例组织学上为弥漫性大b细胞淋巴瘤(DLBCL)。尽管近年来CLL的治疗取得了很大进展,但正如我们的病例报告和综述所总结的那样,在接受新型药物治疗的患者中也会发生RS。方法总结3例联合BTK抑制剂(BTKi)或BCL2抑制剂(BCL2i)治疗的RS患者,并复习文献。结果总结了3例RS患者。患者1在伊鲁替尼减量期间转化为DLBCL,并在利妥昔单抗依托泊苷、地塞米松、阿霉素、环磷酰胺和新碱(R-EDOCH)联合BTKi治疗后实现骨髓(BM)最小残留病(MRD)阴性完全缓解(CR),持续无进展生存期(PFS)超过2年。患者2在诊断时转化,在接受利妥昔单抗、环磷酰胺、阿霉素、长春新碱、强的松(R-CHOP)治疗后,PD1抗体联合胞嘧啶、阿糖糖、顺铂和地塞米松(DHAP)治疗,PD1抗体联合异环磷酰胺、卡铂和依托泊苷(ICE)治疗后进展。患者2在接受利妥昔单抗、吉西他滨和奥沙利铂(R-GemOx)联合BTKi治疗后达到CR。患者3在诊断时转化为CARD11、TP53和ATM突变,在R-EDOCH联合BTKi治疗后进展,在R-GemOx和venetoclax治疗后达到mrd阴性CR,持续3个月。我们总结了利用靶向治疗的新方案,如BTKi、阿卡拉布替尼和检查点抑制,以及精准医学在未来RS治疗试验中的潜在作用。目前正在评估这些方案单独使用或与免疫化疗联合使用的疗效。结论在本研究中,免疫化疗联合BTKi或BCL2i治疗RS的疗效较好,应根据患者既往治疗情况及生物学特点,结合化疗和靶向治疗,优化治疗方案,为每位患者制定个体化的治疗方案。
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引用次数: 0
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Holistic integrative oncology
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