Conversion therapy

转化疗法
  • 文章类型: Journal Article
    背景:全身转换治疗为最初无法切除的肝细胞癌(HCC)患者提供了挽救根治性肝切除术和优越生存结果的机会,但最优转换策略尚不清楚。
    方法:在PubMed上进行了系统的文献检索,EMBASE,WebofScience,Scopus,2007年至2024年期间,Cochrane图书馆专注于报告HCC转化治疗的研究。治疗组分为酪氨酸激酶抑制剂(TKI),TKI加局部治疗(LRT),TKI加抗PD-1治疗(TKI+PD-1),TKI+PD-1+轻轨,免疫检查点抑制剂(ICI)加LRT,阿替珠单抗加贝伐单抗(A+T)组。转换为手术率(CSR),客观反应率(ORR),≥3级治疗相关不良事件(AE),分析总生存期(OS)和无进展生存期(PFS).
    结果:纳入了38项研究和4,042例患者。TKI组合并的CSR为8%(95%CI,5-12%),TKI+LRT组13%(95%CI,8-19%),TKI+PD-1组28%(95%CI,19-37%),TKI+PD-1+LRT组33%(95%CI,25-41%),ICI+LRT组23%(95%CI,1-46%),A+T组为5%(95%CI,3-8%),分别。OS(0.45,95%CI,0.35-0.60)和PFS(0.49,95%CI,0.35-0.70)的合并HR有利于转换手术的生存益处。亚组分析显示,乐伐替尼+PD-1+LRT赋予了更高的企业社会责任35%(95%CI,26-44%),ORR增加了70%(95%CI,56-83%)。
    结论:目前的研究表明,TKI+PD-1+LRT,尤其是lenvatinib+PD-1+LRT,对于最初无法切除的HCC患者,可能是具有可管理的安全性的优良转化疗法。与单独的全身治疗相比,成功的转化治疗有利于优越的OS和PFS。
    背景:国际前瞻性系统评价注册(PROSPERO)(注册码:CRD42024495289)。
    BACKGROUND: Systemic conversion therapy provides patients with initially unresectable hepatocellular carcinoma (HCC) the chance to salvage radical liver resection and superior survival outcomes, but the optimal conversion strategy is unclear.
    METHODS: A systematic literature search was conducted on PubMed, EMBASE, Web of Science, Scopus, and the Cochrane Library between 2007 and 2024 focusing on studies reporting conversion therapy for HCC. The treatment groups were divided into Tyrosine kinase inhibitors (TKI), TKI plus loco-regional therapy (LRT), TKI plus anti-PD-1 therapy (TKI + PD-1), TKI + PD-1 + LRT, immune checkpoint inhibitors (ICI) plus LRT, and Atezolizumab plus bevacizumab (A + T) groups. The conversion to surgery rate (CSR), objective response rate (ORR), grade ≥ 3 treatment-related adverse events (AEs), overall survival (OS) and progression-free survival (PFS) were analyzed.
    RESULTS: 38 studies and 4,042 patients were included. The pooled CSR were 8% (95% CI, 5-12%) in TKI group, 13% (95% CI, 8-19%) in TKI + LRT group, 28% (95% CI, 19-37%) in TKI + PD-1 group, 33% (95% CI, 25-41%) in TKI + PD-1 + LRT group, 23% (95% CI, 1-46%) in ICI + LRT group, and 5% (95% CI, 3-8%) in A + T group, respectively. The pooled HR for OS (0.45, 95% CI, 0.35-0.60) and PFS (0.49, 95% CI, 0.35-0.70) favored survival benefit of conversion surgery. Subgroup analysis revealed that lenvatinib + PD-1 + LRT conferred higher CSR of 35% (95% CI, 26-44%) and increased ORR of 70% (95% CI, 56-83%).
    CONCLUSIONS: The current study indicates that TKI + PD-1 + LRT, especially lenvatinib + PD-1 + LRT, may be the superior conversion therapy with a manageable safety profile for patients with initially unresectable HCC. The successful conversion therapy favors the superior OS and PFS compared with systemic treatment alone.
    BACKGROUND: International prospective register of systematic reviews (PROSPERO) (registration code: CRD 42024495289).
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  • 文章类型: Journal Article
    背景:肝细胞癌是世界范围内的高致死性肿瘤,而中国的发病率和死亡率也相应较高。对于不可切除的肝细胞癌患者,预后往往较差。这项回顾性研究的目的是研究转换疗法对这些患者的影响。
    方法:该研究纳入了18至75岁的患者,这些患者最初被诊断为不可切除的肝细胞癌,并接受了转化治疗。完成手术后,患者接受了病理诊断,显示完全坏死。这项研究是在第一附属医院进行的回顾性研究,浙江大学医学院,从2019年1月到2021年12月。该研究的主要目标是评估总生存期和无复发生存期。
    结果:共纳入60例符合纳入标准的患者。患者的中位年龄为56.6±9.5岁,其中85%是男性。1年总生存率(OS)为98.3%,三年OS为95.6%。1年无复发生存率(RFS)为81.1%,三年RFS为71.4%。在亚组分析中,BCLC0-A期和BCLCB-C期患者的RFS差异无统计学意义(p=0.296).此外,接受术后新辅助治疗的患者和未接受术后新辅助治疗的患者的RFS无统计学差异(p=0.324).
    结论:转换治疗后手术切除可能是最初不可切除的肝细胞癌患者的有希望的治疗方法。预后良好,病理完全缓解。
    BACKGROUND: Hepatocellular carcinoma is a highly lethal tumor worldwide, and China has a correspondingly high incidence and mortality rate. For patients with unresectable hepatocellular carcinoma, the prognosis is often poor. The objective of this retrospective study was to investigate the effects of conversion therapies on these patients.
    METHODS: The study included patients between the ages of 18 and 75 who were initially diagnosed with unresectable hepatocellular carcinoma and received conversion therapy. After completing surgery, the patients underwent pathological diagnosis, which showed complete necrosis. The study was conducted retrospectively at the First Affiliated Hospital, Zhejiang University School of Medicine, from January 2019 to December 2021. The main objectives of the study were to evaluate the overall survival and recurrence-free survival.
    RESULTS: A total of 60 patients who met the inclusion criteria were enrolled. The median age of the patients was 56.6 ± 9.5 years, and 85% of them were male. The one-year overall survival rate (OS) was 98.3%, and the three-year OS was 95.6%. The one-year recurrence-free survival rate (RFS) was 81.1%, and the three-year RFS was 71.4%. In subgroup analysis, there was no statistically significant difference in RFS between patients with BCLC stages 0-A and BCLC stages B-C (p = 0.296). Additionally, there was no statistically significant difference in RFS between patients who received postoperative new adjuvant therapy and those who did not (p = 0.324).
    CONCLUSIONS: Conversion therapy followed by surgical resection could be a promising treatment for patients with initially unresectable hepatocellular carcinoma, and the prognosis is good with a pathological complete response.
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  • 文章类型: Journal Article
    术前免疫化疗和简单化疗诱导方案在局部晚期不可切除食管鳞状细胞癌(ESCC)转化治疗中的临床价值尚不清楚。
    对2020年1月至2022年12月在我院接受转换手术的不可切除的cT4b期ESCC患者进行了回顾性分析。根据术前诱导治疗计划,分为诱导化疗组(iICT组)和诱导化疗组(iCT组).转换手术率,R0切除率,放射学和病理学肿瘤反应,安全,并对短期生存结局进行分析.
    结果显示,共有199例接受术前诱导治疗的cT4b局部晚期不可切除的ESCC患者被纳入本研究。其中,iICT组有64例(32.2%),iCT组135例(67.8%)。客观缓解率(73.5%vs48.9%)和转换手术率(81.3%vs66.7%)有统计学意义的差异,iICT组和iCT组之间(P=0.001和P=0.019)。在接受手术治疗的两组患者中,iICT组和iCT组的R0切除率(94.2%vs82.2%)和病理完全缓解率(23.1%vs6.7%)差异有统计学意义(P=0.043和P=0.004)。3级及以上发生率两组间差异无统计学意义(P=0.928)。iICT组和iCT组的2年EFS分别为76.4%和42.4%,分别,差异具有统计学意义(P=0.006)。
    与单纯化疗相比,PD-1抑制剂与化疗联合使用可以获得更好的中转手术率,局部晚期不可切除的ESCC的转换治疗中的肿瘤反应和无事件生存期.
    UNASSIGNED: The clinical value of preoperative immunochemotherapy and simple chemotherapy induction regimen in the conversion therapy of locally advanced unresectable esophageal squamous cell carcinoma (ESCC) is still unclear.
    UNASSIGNED: Retrospective analysis was conducted on patients with unresectable cT4b stage ESCC who underwent conversion surgery in our hospital from January 2020 to December 2022. According to the preoperative induction treatment plan, they were divided into induction immunochemotherapy group (iICT group) and induction chemotherapy group (iCT group). The conversion surgery rate, R0 resection rate, radiological and pathological tumor responses, safety, and short-term survival outcomes were analyzed.
    UNASSIGNED: The results showed that a total of 199 patients with cT4b locally advanced unresectable ESCC who underwent preoperative induction therapy were included in this study. Among them, there were 64 cases (32.2%) in the iICT group, 135 cases (67.8%) in the iCT group. There was a statistically significant difference in objective response rate (73.5% vs 48.9%) and conversion surgery rate (81.3% vs 66.7%), between the iICT and iCT groups (P=0.001 and P=0.019). Among the two groups of patients who underwent surgery, there were statistically significant differences in R0 resection rate (94.2% vs 82.2%) and pathological complete remission rate (23.1% vs 6.7%) between the iICT and iCT groups (P=0.043 and P=0.004). And there was no statistically significant difference in the incidence of grade 3 and above between two groups (P=0.928). The 2-year EFS of the iICT group and iCT group were 76.4% and 42.4%, respectively, with statistically significant differences (P=0.006).
    UNASSIGNED: Compared with simple chemotherapy, the combination of PD-1 inhibitors and chemotherapy can achieve better conversion surgery rate, tumor response and event-free survival in the conversion therapy of locally advanced unresectable ESCC.
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    文章类型: Journal Article
    在过去的十年里,因可能的性别烦躁不安而转诊到性别诊所的儿童和青少年数量大幅增加.性别确认护理模式,在加拿大占主导地位的治疗方法,是基于低质量的证据。其他国家正在意识到这一点,并将社会心理治疗和/或探索性心理治疗作为年轻患者性别相关痛苦的一线治疗方法。心理动力学(探索性)心理治疗已经确立了对一系列疾病的疗效,并已用于患有性别烦躁不安的年轻人和成年人。在加拿大,一些学者认为,采用心理动力学心理疗法治疗性别焦虑受到阻碍,他们认为这可能违反了反对转化疗法的法律。心理动力心理治疗不是转化疗法,应在加拿大作为性别烦躁不安的治疗方式提供。
    Over the last ten years, there has been a substantial increase in the number of children and adolescents referred to gender clinics for possible gender dysphoria. The gender affirming model of care, a dominant treatment approach in Canada, is based on low quality evidence. Other countries are realizing this and making psychosocial treatments and/or exploratory psychotherapy a first line of treatment for gender related distress in young patients. Psychodynamic (exploratory) psychotherapy has established efficacy for a range of conditions, and has been used in youth and adults with gender dysphoria. In Canada, the adoption of psychodynamic psychotherapy for gender dysphoria is impeded by some academics who argue that it may violate laws against conversion therapy. Psychodynamic psychotherapy is not conversion therapy and should be made available in Canada as a treatment modality for gender dysphoria.
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  • 文章类型: Journal Article
    性取向和性别认同/表达改变努力(SOGIECE)是信誉不佳的做法,与严重的负面影响有关,与临床实践的现代标准不符。尽管有证据表明SOGIECEs与严重的医源性影响有关,尽管支持LGBTQ+肯定护理替代品,SOGIECE做法仍然存在。在1970年代和1980年代,行为疗法发表的文章测试和/或认可SOGIECE,从而促进他们的全面发展,接受,和使用。组织了行为疗法工作组,以对行为疗法上发表的SOGIECE文章进行严格的审查,并决定是否,什么,应该对这些条款采取正式行动。本报告对行为疗法上发表的SOGIECE历史文献进行了详细的回顾,并概述了工作队的审议和民主过程,从而采取了以下行动:(1)以数字形式向k=24篇SOGIECE论文添加突出的咨询信息“黑匣子”免责声明,警告读者这些论文中测试或描述的SOGIECE实践与现代标准不一致,(2)抵消这些论文发表的组织财务收益,(3)推广LGBTQ+肯定做法。SOGIECE并不是该领域历史上唯一涉及的实践,今天的科学期刊的页面包括与明天的道德标准和道德准则不一致的实践。本报告呼吁采取预防措施和编辑保障措施,以最大程度地减少存在问题的奖学金的未来可能性和影响。包括需要在临床科学和同行评审的各个方面充分包括具有相关生活经验的人。
    Sexual orientation and gender identity/expression change efforts (SOGIECEs) are discredited practices that are associated with serious negative effects and incompatible with modern standards for clinical practice. Despite evidence linking SOGIECEs with serious iatrogenic effects, and despite support for LGBTQ+-affirmative care alternatives, SOGIECE practices persist. In the 1970s and 1980s, Behavior Therapy published articles testing and/or endorsing SOGIECEs, thereby contributing to their overall development, acceptance, and use. The Behavior Therapy Task Force on SOGIECEs was assembled to conduct a rigorous review of the SOGIECE articles published in Behavior Therapy and to decide whether, and what, formal action(s) should be taken on these articles. This report provides a detailed review of the historic SOGIECE literature published in Behavior Therapy and outlines the Task Force\'s deliberative and democratic processes resulting in actions to: (1) add prominent advisory information to k = 24 SOGIECE papers in the form of digital \"black box\" disclaimers that caution readers that the SOGIECE practices tested or described in these papers are inconsistent with modern standards, (2) offset organizational financial benefits from the publication of these papers, and (3) promote LGBTQ+-affirmative practices. SOGIECEs are not the only concerning practices across the field\'s history, and the pages of today\'s scientific journals include practices that will be at odds with tomorrow\'s moral standards and ethical guidelines. This report calls for precautionary measures and editorial safeguards to minimize the future likelihood and impact of problematic published scholarship, including the need to fully include those with relevant lived experiences in all aspects of clinical science and peer review.
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  • 文章类型: Journal Article
    基于免疫检查点抑制剂(ICI)的治疗在各种癌症类型中取得了令人印象深刻的成功。近十年来,几种ICI被空前批准为晚期肝细胞癌(HCC)的治疗方案。同时,正在进行许多临床试验,以利用更多的ICIs进入最初不可切除的HCC和术后HCC,以预期诱导足够的肿瘤降级以进一步切除或实施辅助治疗以实现无复发生存。分别。在这次审查中,我们的目的是总结一些语用的组织形态学,免疫组织化学,和分子病理参数有望表明新辅助/转化ICI相关治疗的反应,并预测辅助/治疗性ICI相关治疗对HCC的疗效。
    我们使用术语肝细胞癌搜索PubMed,免疫疗法,免疫检查点抑制剂,免疫检查点封锁,转换疗法,新辅助治疗,辅助治疗,生物标志物,病理评估,病理评估至2023年2月。
    尽管对相关HCC标本的病理评估尚无共识,令人鼓舞的是,一些研究集中在这个领域,而且,其他类型癌症的方法和参数也值得参考。对于接受免疫治疗的HCC标本的病理评估,一个合适的抽样方案,识别免疫疗法相关的病理反应,应强调病理反应率的量化。对于计划接受免疫治疗的HCC患者,肿瘤浸润淋巴细胞,肿瘤内三级淋巴结构,程序性细胞死亡配体1,Wnt/β-catenin,微卫星不稳定性和错配修复,肿瘤突变负荷和肿瘤新抗原,以及其他一些信号通路是ICI治疗反应的潜在预测生物标志物。
    免疫治疗时代的HCC管理出现了一个全新的病理学挑战,即提供与免疫治疗相关的诊断报告。尽管许多相关研究是临床前或不足的,它们可能在未来极大地改变HCC的免疫治疗策略。
    UNASSIGNED: Immune checkpoint inhibitor (ICI)-based therapy has achieved impressive success in various cancer types. Several ICIs have been unprecedentedly approved as the treatment regimens for advanced hepatocellular carcinoma (HCC) in recent decade. Meanwhile, numerous clinical trials are being performed to exploit more ICIs into initially unresectable HCC and postoperative HCC to expectantly induce adequate tumor downstaging for further resection or implement adjuvant treatment for relapse-free survival, respectively. In this review, we aim to summarize some pragmatic histomorphologic, immunohistochemical, and molecular pathologic parameters which promisingly indicate the response of neoadjuvant/conversion ICI-related therapy and predict the efficacy of adjuvant/therapeutic ICI-related therapy for HCC.
    UNASSIGNED: We searched PubMed using the terms hepatocellular carcinoma, immunotherapy, immune checkpoint inhibitor, immune checkpoint blockade, conversion therapy, neoadjuvant therapy, adjuvant therapy, biomarker, pathologic evaluation, pathologic assessment till February 2023.
    UNASSIGNED: Although there is no consensus regarding the pathologic evaluation of relevant HCC specimens, it is encouraging that a few of studies have concentrated on this field, and moreover, the methods and parameters noted on other cancer types are also worthy of reference. For the pathologic assessment of HCC specimens underwent immunotherapy, a suitable sampling scheme, identifying immunotherapy-related pathologic response, and quantification of pathologic response rate should be emphasized. For the patients of HCC who are scheduled to receive immunotherapy, tumor-infiltrating lymphocyte, intratumoral tertiary lymphoid structure, programmed cell death ligand 1, Wnt/β-catenin, microsatellite instability and mismatch repair, tumor mutational burden and tumor neoantigen, as well as some other signaling pathways are the potential predictive biomarkers of treatment response of ICI.
    UNASSIGNED: The management of HCC in the era of immunotherapy arises a brand-new pathological challenge that is to provide an immunotherapy-related diagnostic report. Albeit many related researches are preclinical or insufficient, they may tremendously alter the immunotherapy strategy of HCC in future.
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  • 文章类型: Journal Article
    背景:局部治疗可能与免疫治疗和靶向药物协同作用。本研究旨在评估经导管动脉化疗栓塞(TACE)和肝动脉灌注化疗(HAIC)联合酪氨酸激酶抑制剂(TKIs)和程序性死亡-1(PD-1)抑制剂在最初不可切除的肝细胞癌(uHCC)患者中的有效性和安全性。
    方法:对2020年7月至2023年2月接受TACE-HAIC联合TKIs和PD-1抑制剂联合治疗的最初诊断为uHCC的患者进行了回顾性研究。主要终点是总生存期(OS)和无进展生存期(PFS)和不良事件(AE)。客观反应率(ORR),疾病控制率(DCR)和转换手术率(CSR),而次要终点。
    结果:筛选后,本研究共选择62例患者.总体中位OS为18.2个月(95%CI16.24-20.16),中位PFS为9.2个月(95%CI7.24-11.16)。基于改良的实体瘤反应评估标准(mRECIST)标准和RECISTv1.1标准,ORR为67.7%(42/62),DCR为90.3%(56/62),CSR为27.4%(17/62)。最常见的治疗引起的不良事件(TEAE)是转氨酶(56.4%,35/62),恶心和呕吐(43.5%,27/62),血小板减少症(37.1%,23/62),腹痛(33.9%,21/62),和发烧(33.9%,21/62).
    结论:TKIs与PD-1抑制剂联合TACE-HAIC治疗是uHCC患者的一种有效且可耐受的治疗选择。联合治疗后接受手术的患者可能具有生存益处。
    BACKGROUND: Local treatment may function synergistically with immunotherapy and targeted agents. This study aimed to assess the effectiveness and safety of transcatheter arterial chemoembolization (TACE) and hepatic artery infusion chemotherapy (HAIC) combined with tyrosine kinase inhibitors (TKIs) and programmed death-1 (PD-1) inhibitors in patients with initially unresectable hepatocellular carcinoma (uHCC).
    METHODS: A retrospective study was conducted on patients diagnosed with initially uHCC who received combined treatment of TACE-HAIC combined with TKIs and PD-1 inhibitors from July 2020 to February 2023. The primary endpoints were overall survival (OS) and progression free survival (PFS) and adverse events (AEs). Objective response rate (ORR), disease control rate (DCR) and conversion surgery rate (CSR), whereas the secondary endpoints.
    RESULTS: After screening, a total of 62 patients were selected for this study. The overall median OS was 18.2 (95% CI 16.24-20.16) months and median PFS was 9.2 (95% CI 7.24-11.16) months. Based on the modified Response Evaluation Criteria in Solid Tumors (mRECIST) criteria and RECIST v1.1 criteria, ORR was 67.7% (42/62), and the DCR was 90.3% (56/62), the CSR was 27.4% (17/62). The most common treatment-emergent adverse events (TEAEs) were transaminitis (56.4%, 35/62), nausea and vomiting (43.5%, 27/62), thrombocytopenia (37.1%, 23/62), abdominal pain (33.9%, 21/62), and fever (33.9%, 21/62).
    CONCLUSIONS: TKIs combined with PD-1 inhibitors plus TACE-HAIC therapy represents an effective and tolerable treatment option in patients with uHCC. Patients undergoing surgery after combination therapy may have survival benefits.
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  • 文章类型: Journal Article
    晚期肝细胞癌(HCC)的术前转化治疗仍在探索中。这项研究报道了联合经肝动脉化疗栓塞(TACE)的潜力,肝动脉灌注化疗(HAIC),程序性细胞死亡蛋白-1(PD-1)抑制剂和乐伐替尼作为非转移性晚期HCC的术前转换治疗。
    这项回顾性研究收集了接受这种联合治疗的非转移性晚期HCC患者的数据。我们在TACE中使用药物洗脱珠(DEB)代替常规碘化油。临床数据,转化率,对不良事件(AE)和短期生存率进行了总结.根据患者是否接受手术进行分层分析。
    共28例患者纳入分析。没有观察到4级AE。总客观有效率(ORR)为64.3%。10例(35.7%)患者在2个周期的联合治疗后最终接受了R0切除。成功切除的患者(手术组)的ORR明显较高(90.0%vs.50.0%,P=0.048)。手术组中甲胎蛋白(AFP)>1,000µg/L的患者比例显着降低(10.0%vs.66.7%,P=0.006)。联合治疗后,更多的手术组患者AFP水平显着降低>90%(75.0%vs.23.1%,P=0.03),以及原发性肿瘤和门静脉肿瘤血栓形成(PVTT)中18F-氟脱氧葡萄糖(18F-FDG)的标准化摄取值(SUV)(60.0%vs.5.6%,P=0.003;57.1%vs.8.3%,P=0.04)。值得注意的是,85.7%的PVTT在病理检查中表现出主要病理反应(MPR),尽管在术前影像学检查中只有28.6%达到了下降阶段。MPR在PVTT中比在主要肿瘤中更常见(85.7%vs.20.0%)。在非手术组中,中位总生存期(OS)为7个月,1年生存率为27.8%,在手术组,中位OS未达到,1年生存率为60.0%.
    TACE-HAIC的组合,PD-1抑制剂和lenvatinib显示出其作为非转移性晚期HCC的术前转换治疗的益处。除了影像学评估,18F-FDG摄取和AFP的显着减少可以用作成功转化的预测因子,尤其是PVTT。
    UNASSIGNED: The preoperative conversion therapy for advanced hepatocellular carcinoma (HCC) is still being explored. This study reported the potential of combination of transarterial chemoembolization (TACE), hepatic arterial infusion chemotherapy (HAIC), programmed cell death protein-1 (PD-1) inhibitors and lenvatinib as preoperative conversion therapy for nonmetastatic advanced HCC.
    UNASSIGNED: This retrospective study gathered data on patients with nonmetastatic advanced HCC who received this combination therapy. We used drug-eluting bead (DEB) instead of conventional iodized oil in TACE. The clinical data, conversion rate, adverse events (AEs) and short-term survival were summarized. A stratified analysis based on whether or not the patient received surgery was conducted.
    UNASSIGNED: A total of 28 patients were included in the analysis. No grade 4 AEs were observed. The overall objective response rate (ORR) was 64.3%. Ten (35.7%) patients eventually received R0 resection after 2 cycles of combination therapy. Patients succeeding to resection (surgery group) had significantly higher ORR (90.0% vs. 50.0%, P=0.048). The proportion of patients with alpha-fetoprotein (AFP) >1,000 µg/L was significantly lower in surgery group (10.0% vs. 66.7%, P=0.006). After combination therapy, more patients in surgery group experienced significant reduction of >90% in AFP levels (75.0% vs. 23.1%, P=0.03), as well as standardized uptake value (SUV) of 18F-fluorodeoxyglucose (18F-FDG) both in primary tumors and portal vein tumor thrombosis (PVTT) (60.0% vs. 5.6%, P=0.003; 57.1% vs. 8.3%, P=0.04). Of note, 85.7% of PVTT exhibited major pathological response (MPR) in pathological examination although only 28.6% achieved downstage in preoperative imaging examination. MPR was more commonly observed in PVTT than in main tumors (85.7% vs. 20.0%). In non-surgery group, the median overall survival (OS) was 7 months with a 1-year survival rate of 27.8%, while in surgery group, the median OS was not reached and 1-year survival rate was 60.0%.
    UNASSIGNED: The combination of TACE-HAIC, PD-1 inhibitors and lenvatinib showed its benefit as a preoperative conversion therapy for nonmetastatic advanced HCC. In addition to imaging evaluation, significant reduction of 18F-FDG uptake and AFP can be used as predictors of successful conversion, especially for PVTT.
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