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Richter transformation: biological insights, diagnostic challenges and emerging therapies. 里希特转化:生物学见解,诊断挑战和新兴疗法。
IF 2.4 4区 医学 Q2 ONCOLOGY Pub Date : 2025-09-01 Epub Date: 2025-07-04 DOI: 10.1097/CCO.0000000000001173
Romain Guièze

Purpose of review: this review aims to underscore the significance of the growing number of advances related to Richter transformation (RT), an aggressive form of lymphoma arising in patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma.

Recent findings: The development of sequencing analytic tools and single-cell approaches has overcome the major challenge of cellular admixture in RT, enabling a deeper understanding of the genetic alterations driving transformation from CLL to RT. These techniques have also made it possible to detect RT clones long before clinical onset. In parallel, novel targeted therapies for CLL and immunotherapeutic strategies for lymphomas are offering renewed hope. Recent phase 2 studies notably support the potential role of immune checkpoint inhibitors and bispecific T-cell engagers in RT, while experience with chimeric antigen receptor T-cell therapies continues to grow, raising hopes for improved outcomes in this historically difficult-to-treat condition.

Summary: recent research is focusing on better understanding the transformation process, improving the early detection of RT, and developing novel targeted and immunotherapy treatments and combinations for patients with RT.

综述目的:本综述旨在强调Richter转化(RT)相关进展的重要性,RT是一种发生在慢性淋巴细胞白血病(CLL)或小淋巴细胞淋巴瘤患者中的侵袭性淋巴瘤。最近的发现:测序分析工具和单细胞方法的发展已经克服了RT中细胞混合物的主要挑战,使人们能够更深入地了解从CLL到RT转化的遗传改变。这些技术也使得在临床发病前很长时间检测RT克隆成为可能。与此同时,针对CLL的新型靶向治疗和针对淋巴瘤的免疫治疗策略也带来了新的希望。最近的2期研究明显支持免疫检查点抑制剂和双特异性t细胞参与者在RT中的潜在作用,而嵌合抗原受体t细胞疗法的经验继续增长,提高了改善这种历史上难以治疗的疾病的结果的希望。摘要:近年来的研究重点是更好地了解肿瘤的转化过程,提高对肿瘤的早期发现,开发新的靶向和免疫治疗方法及联合治疗肿瘤患者。
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引用次数: 0
Perspectives on T-cell engaging therapies in relapsed/refractory indolent non-Hodgkin lymphoma. t细胞参与治疗复发/难治性惰性非霍奇金淋巴瘤的前景
IF 2.4 4区 医学 Q2 ONCOLOGY Pub Date : 2025-09-01 Epub Date: 2025-06-05 DOI: 10.1097/CCO.0000000000001160
Max Bakker, Maria T Kuipers, Marie José Kersten, Sanne H Tonino, Yasmina I M Serroukh

Purpose of review: Follicular lymphoma (FL) and marginal zone lymphoma (MZL) are indolent subtypes of non-Hodgkin lymphoma (iNHL) characterized by a relapsing-remitting disease course. A promising novel therapeutic class emerges with T-cell engaging therapies, which include CD19 directed chimeric antigen receptor T-cell (CAR-T) therapy and CD3xCD20 directed bispecific antibodies (BsABs). This review provides a comprehensive evaluation of their efficacy and safety along with logistical considerations in relapsed/refractory (r/r) iNHL.

Recent findings: Several pivotal CAR-T trials have presented impressive response rates and durable remissions in r/r FL, while data in MZL is scarce. CAR-T is given as a single infusion, but requires a complex logistical infrastructure. Different BsAbs have shown favorable efficacy with a lower rate of acute toxicities. Off-the-shelve availability favors its usability, although prolonged administration of BsAbs might impose a substantial burden for patients. Long-term infection risk is a concern for both treatments. Clinical studies that directly compare CAR-T and BsAbs are still lacking.

Summary: Both CAR-T and BsAbs have demonstrated promising efficacy as treatment modalities in iNHL. Decision making for T-cell engaging therapies should be tailored to patient specific factors and availability. Maturation of follow-up data will further guide evidence-based treatment choices in FL and MZL.

综述目的:滤泡性淋巴瘤(FL)和边缘区淋巴瘤(MZL)是非霍奇金淋巴瘤(iNHL)的惰性亚型,其特点是疾病过程复发缓解。一种有前景的新型治疗方法是t细胞结合疗法,包括CD19定向嵌合抗原受体t细胞(CAR-T)疗法和CD3xCD20定向双特异性抗体(BsABs)。这篇综述提供了它们在复发/难治性iNHL (r/r)中的有效性和安全性以及后勤考虑的综合评价。最近的发现:几个关键的CAR-T试验在r/r FL中显示了令人印象深刻的缓解率和持久的缓解,而MZL的数据很少。CAR-T是单次输注,但需要复杂的后勤基础设施。不同的bsab显示出良好的疗效和较低的急性毒性发生率。尽管长期服用bsab可能会给患者带来沉重的负担,但现货供应有利于其可用性。长期感染风险是这两种治疗的一个问题。直接比较CAR-T和bsab的临床研究仍然缺乏。摘要:CAR-T和bsab作为治疗iNHL的方法都显示出了良好的疗效。t细胞介入疗法的决策应根据患者的具体因素和可用性进行调整。成熟的随访数据将进一步指导FL和MZL的循证治疗选择。
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引用次数: 0
Advantages of robotic surgery in obese patients with endometrial cancer. 机器人手术在肥胖子宫内膜癌患者中的优势。
IF 2.4 4区 医学 Q2 ONCOLOGY Pub Date : 2025-09-01 Epub Date: 2025-05-14 DOI: 10.1097/CCO.0000000000001156
François Zaccarini, Henrik Falconer

Purpose of review: Endometrial cancer is the most common gynecological cancer among women in high-income countries and the prevalence is projected to increase worldwide because of the obesity epidemic. Surgery is a key step in the management of endometrial cancer. Performing surgery and delivering care to obese patients (BMI ≥ 30 kg/m 2 ) and especially to morbidly obese patients (BMI ≥ 40 kg/m 2 ) is challenging.This review focuses on the advantages of robotic surgery in obese patients with endometrial cancer.

Recent findings: The emergence of robotic surgery is associated with increasing rates of minimally invasive surgery for endometrial cancer. Robotic surgery offers several advantages over conventional laparoscopy, especially in obese patients with endometrial cancer which has led to decreasing rates of conversion to laparotomy. The approach allows surgical staging on obese and morbidly obese patients without increasing complication rates or the length of hospital stay, while improving ergonomics for the surgeon.

Summary: Robotic surgery should be the preferred approach for obese patients with endometrial cancer. Current data confirm its safety and benefits for this group of women, particularly for obese patients with a BMI ≥ 40 kg/m 2 .

综述目的:子宫内膜癌是高收入国家妇女中最常见的妇科癌症,由于肥胖的流行,预计其患病率将在全球范围内增加。手术是治疗子宫内膜癌的关键步骤。对肥胖患者(BMI≥30 kg/m2),特别是病态肥胖患者(BMI≥40 kg/m2)进行手术和护理具有挑战性。本文综述了机器人手术在肥胖子宫内膜癌患者中的优势。最近发现:机器人手术的出现与子宫内膜癌微创手术率的增加有关。与传统的腹腔镜手术相比,机器人手术有几个优点,特别是在患有子宫内膜癌的肥胖患者中,这导致转向剖腹手术的比率降低。该方法允许对肥胖和病态肥胖患者进行手术分期,而不会增加并发症发生率或住院时间,同时改善外科医生的人体工程学。摘要:机器人手术应该是肥胖子宫内膜癌患者的首选方法。目前的数据证实了其对这组女性的安全性和益处,特别是对BMI≥40 kg/m2的肥胖患者。
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引用次数: 0
Current role and indications of minimally invasive surgery in gynecologic oncology. 微创手术在妇科肿瘤中的作用及适应证。
IF 2.4 4区 医学 Q2 ONCOLOGY Pub Date : 2025-09-01 Epub Date: 2025-08-07 DOI: 10.1097/CCO.0000000000001157
Ignacio Zapardiel
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引用次数: 0
The evolving treatment paradigm of chimeric antigen receptor T-cell therapy in lymphoma. 嵌合抗原受体t细胞治疗淋巴瘤的发展模式。
IF 2.4 4区 医学 Q2 ONCOLOGY Pub Date : 2025-09-01 Epub Date: 2025-07-07 DOI: 10.1097/CCO.0000000000001169
Paolo Lopedote, John H Baird

Purpose of review: The field of chimeric antigen receptor (CAR) T-cell therapies is rapidly evolving. The number of approved indications for the existing CAR-T products is increasing, and, in parallel, so too is the number of novel products and disease targets being evaluated. Being able to navigate the available evidence is a priority for every hemato-oncologist.

Recent findings: Long-term follow up from pivotal trials, as well as real-world studies of commercial products in a range of B-cell non-Hodgkin lymphoma (B-NHL) have confirmed their ability to produce durable disease control with a manageable toxicity profile in a significant proportion of patients, including populations generally excluded from clinical trials. Nonrelapse morbidity and mortality risk profiles have been better established with long-term follow up, and risk reduction via antimicrobial prophylaxis and monitoring of hematologic recovery are being integrated as part of standard of care for these patients beyond the first-year posttreatment.

Summary: A significant proportion of B-NHL patients can achieve long-lasting remission after CAR-T. Ongoing efforts have identified demographic and disease characteristics associated with optimal response and toxicity. Novel products targeting alternative B-cell antigens or utilizing an allogeneic platform might be an option for those whose disease recurs after anti-CD19 CAR-T, with multiple studies ongoing to define their role in the treatment algorithm.

综述目的:嵌合抗原受体(CAR) t细胞治疗领域正在迅速发展。现有CAR-T产品获批适应症的数量正在增加,与此同时,正在评估的新产品和疾病靶点的数量也在增加。能够驾驭现有的证据是每个血液肿瘤学家的首要任务。最近的发现:关键试验的长期随访,以及对一系列b细胞非霍奇金淋巴瘤(B-NHL)的商业产品的实际研究,证实了它们能够在很大比例的患者(包括通常被排除在临床试验之外的人群)中产生持久的疾病控制和可管理的毒性特征。通过长期随访已经更好地建立了非复发发病率和死亡率风险谱,并且通过抗菌素预防和血液学恢复监测来降低风险正在被纳入这些患者治疗一年后的标准护理的一部分。总结:相当比例的B-NHL患者在CAR-T后可以获得长期缓解。正在进行的工作已经确定了与最佳反应和毒性相关的人口统计学和疾病特征。针对替代b细胞抗原或利用同种异体平台的新产品可能是抗cd19 CAR-T后疾病复发的一种选择,目前正在进行多项研究以确定它们在治疗算法中的作用。
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引用次数: 0
Benefits of laparoscopic approach in early-stage ovarian cancer and ovarian masses. 腹腔镜入路治疗早期卵巢癌和卵巢肿块的益处。
IF 2.4 4区 医学 Q2 ONCOLOGY Pub Date : 2025-09-01 Epub Date: 2025-05-21 DOI: 10.1097/CCO.0000000000001159
María Alonso-Espías, Myriam Gracia, Ignacio Zapardiel

Purpose of review: The aim of this review is to summarize the available evidence on the use and benefits of minimally invasive surgery (MIS) in the management of ovarian masses and early-stage ovarian cancer.

Recent findings: MIS did not negatively impact survival outcomes or increase perioperative complication rates in patients with early-stage ovarian cancer compared to open surgery, while providing the inherent benefits associated with this surgical approach. Regarding the type of MIS, both laparoscopic and robotic approaches can be used in well selected patients at specialized centers.

Summary: MIS appears to be a feasible and well tolerated surgical option for the evaluation of ovarian masses and for the comprehensive staging of early-stage ovarian cancer patients. Compared to open surgery, MIS offers several advantages, including significantly reduced blood loss, a lower need for transfusion, shorter hospital stays and faster postoperative recovery, without compromising surgical results. Furthermore, extensive retrospective studies have shown comparable survival outcomes between both approaches. However, high-quality evidence from randomized clinical trials is still needed to establish definitive conclusions and draw international recommendations.

综述目的:本综述的目的是总结微创手术(MIS)在卵巢肿块和早期卵巢癌治疗中的应用和益处的现有证据。最近的研究发现:与开放手术相比,MIS对早期卵巢癌患者的生存结果没有负面影响,也没有增加围手术期并发症的发生率,同时提供了与该手术方法相关的固有益处。关于MIS的类型,腹腔镜和机器人方法都可以在专业中心用于精心挑选的患者。摘要:MIS似乎是评估卵巢肿块和早期卵巢癌患者综合分期的一种可行且耐受性良好的手术选择。与开放手术相比,MIS具有几个优势,包括显著减少失血量、更少的输血需求、更短的住院时间和更快的术后恢复,而不会影响手术效果。此外,广泛的回顾性研究表明,两种方法之间的生存结果相当。然而,仍然需要来自随机临床试验的高质量证据来建立明确的结论并提出国际建议。
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引用次数: 0
Liquid biopsy in breast cancer: promises and challenges. 乳腺癌液体活检:希望与挑战。
IF 2.4 4区 医学 Q2 ONCOLOGY Pub Date : 2025-09-01 Epub Date: 2025-07-02 DOI: 10.1097/CCO.0000000000001168
Sotiris Loizidis, Maria-Alexandra Stanciu, Michail Ignatiadis

Purpose of review: This review aims to provide the latest updates regarding circulating tumor DNA (ctDNA) applications in breast cancer. We discuss the current indications and recent research efforts including important ongoing trials.

Recent findings: In the metastatic setting, ctDNA has an established role for identifying druggable mutations (e.g. PIK3CA, ESR1, etc.). Various ctDNA assays used in randomized trials have been approved by regulatory authorities as companion diagnostic devices. Beyond precision medicine, emerging evidence indicates that ctDNA could be used for disease monitoring and detecting acquired resistance mechanisms. In the early setting, two types of ctDNA detection assays can be used: tumor-agnostic and tumor-informed, both having pros and cons. The clinical utility of ctDNA as a surveillance tool for patients with early breast cancer after treatment with curative intent is under investigation. Moreover, many research groups have demonstrated the potential role of ctDNA as a biomarker for assessing response to neoadjuvant systemic treatment and modification of therapeutic plan.

Summary: CtDNA is currently used in metastatic breast cancer for treatment selection, and its clinical utility in early breast cancer is prospectively evaluated.

综述目的:本综述旨在提供循环肿瘤DNA (ctDNA)在乳腺癌中的应用的最新进展。我们讨论目前的适应症和最近的研究工作,包括重要的正在进行的试验。最近的研究发现:在转移性肿瘤中,ctDNA在鉴定可药物突变(如PIK3CA、ESR1等)方面具有确定的作用。在随机试验中使用的各种ctDNA测定已被监管机构批准作为伴随诊断设备。除了精准医学,新出现的证据表明,ctDNA可以用于疾病监测和检测获得性耐药机制。在早期,可以使用两种类型的ctDNA检测分析:肿瘤不可知论和肿瘤信息,两者都有利弊。ctDNA作为早期乳腺癌患者在治疗后的监测工具的临床应用正在研究中。此外,许多研究小组已经证明了ctDNA作为评估新辅助全身治疗反应和修改治疗计划的生物标志物的潜在作用。摘要:CtDNA目前被用于转移性乳腺癌的治疗选择,其在早期乳腺癌中的临床应用被前瞻性评估。
{"title":"Liquid biopsy in breast cancer: promises and challenges.","authors":"Sotiris Loizidis, Maria-Alexandra Stanciu, Michail Ignatiadis","doi":"10.1097/CCO.0000000000001168","DOIUrl":"10.1097/CCO.0000000000001168","url":null,"abstract":"<p><strong>Purpose of review: </strong>This review aims to provide the latest updates regarding circulating tumor DNA (ctDNA) applications in breast cancer. We discuss the current indications and recent research efforts including important ongoing trials.</p><p><strong>Recent findings: </strong>In the metastatic setting, ctDNA has an established role for identifying druggable mutations (e.g. PIK3CA, ESR1, etc.). Various ctDNA assays used in randomized trials have been approved by regulatory authorities as companion diagnostic devices. Beyond precision medicine, emerging evidence indicates that ctDNA could be used for disease monitoring and detecting acquired resistance mechanisms. In the early setting, two types of ctDNA detection assays can be used: tumor-agnostic and tumor-informed, both having pros and cons. The clinical utility of ctDNA as a surveillance tool for patients with early breast cancer after treatment with curative intent is under investigation. Moreover, many research groups have demonstrated the potential role of ctDNA as a biomarker for assessing response to neoadjuvant systemic treatment and modification of therapeutic plan.</p><p><strong>Summary: </strong>CtDNA is currently used in metastatic breast cancer for treatment selection, and its clinical utility in early breast cancer is prospectively evaluated.</p>","PeriodicalId":10893,"journal":{"name":"Current Opinion in Oncology","volume":" ","pages":"512-521"},"PeriodicalIF":2.4,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144625509","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Psychological interventions in adolescents and young adults with cancer: a scoping review targeting protective factors of resilience. 青少年和青年癌症患者的心理干预:针对恢复力保护因素的范围综述。
IF 2.8 4区 医学 Q2 ONCOLOGY Pub Date : 2025-07-01 Epub Date: 2025-05-02 DOI: 10.1097/CCO.0000000000001151
Zoé Servais, Yves Libert, Charlotte Grégoire, Magali Lahaye, Isabelle Merckaert

Purpose of review: Psychological interventions are essential for adolescents and young adults with cancer (AYACs), who experience poor outcomes in their emotional health, social functioning, health behaviors, and cancer-related cognitive impairments (CRCI). This scoping review synthesizes and discusses recent interventions aiming to promote resilience in AYAs with cancer up to 39 years old. The aim is to identify effective intervention strategies and highlight gaps in current research.

Recent findings: Twelve studies were identified, covering interventions targeting physical health, cognition and behavior, social support, emotion regulation, and neurobiology. Most interventions focused on physical activity and cognitive-behavioral approaches, demonstrating positive effects on psychological distress, self-efficacy and quality of life. However, there is a lack of interventions addressing social support, neurobiological resilience, and emotion regulation, despite their well established role in fostering adaptation to adversity.

Summary: Findings underscore the importance of integrative, multimodal approaches for resilience-building in AYACs. Future research should prioritize interventions that incorporate social, emotional, and neurobiological dimensions while ensuring accessibility through digital health solutions. Additionally, early implementation of psychological interventions during the initial cancer treatment period could be critical for mitigating long-term psychological distress and cognitive impairments. Co-constructing interventions with AYACs through participatory approaches is essential to enhance their effectiveness.

综述目的:心理干预对于在情绪健康、社会功能、健康行为和癌症相关认知障碍(CRCI)方面表现不佳的青少年和年轻癌症患者(AYACs)至关重要。本综述综合并讨论了旨在促进39岁以下癌症aya患者恢复能力的近期干预措施。目的是确定有效的干预策略,并突出当前研究中的差距。最新发现:12项研究被确定,涵盖了针对身体健康、认知和行为、社会支持、情绪调节和神经生物学的干预措施。大多数干预措施侧重于身体活动和认知行为方法,显示出对心理困扰、自我效能和生活质量的积极影响。然而,缺乏针对社会支持、神经生物学弹性和情绪调节的干预措施,尽管它们在促进逆境适应方面发挥了良好的作用。总结:研究结果强调了综合、多模式的方法对农村地区抗灾能力建设的重要性。未来的研究应优先考虑结合社会、情感和神经生物学维度的干预措施,同时确保通过数字健康解决方案的可及性。此外,在癌症治疗初期早期实施心理干预对于减轻长期心理困扰和认知障碍至关重要。通过参与性方法与ayac共同构建干预措施对于提高其有效性至关重要。
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引用次数: 0
Implementing an integrative oncology pathway in a comprehensive cancer center: expert insights and perspectives. 在综合性癌症中心实施整合肿瘤学途径:专家见解和观点。
IF 2.8 4区 医学 Q2 ONCOLOGY Pub Date : 2025-07-01 Epub Date: 2025-04-23 DOI: 10.1097/CCO.0000000000001150
Marie-Aline Echterbille, Florence Horicks, Jennifer Dhont, Virginie De Wilde

Purpose of review: Integrative oncology (IO) has evolved into an evidence-informed discipline endorsed by major oncology organizations. However, integrating IO into standard oncology care remains a challenge, often dependent on institutional culture and provider attitudes. This exploratory pilot study aimed to assess healthcare professionals' (HCPs) knowledge, communication practices, perceived needs, and perspectives regarding IO in a Belgian Comprehensive Cancer Center with no preexisting IO pathway.

Recent findings: Among the 33 participants, 45% understood IO as a patient-centered approach, while 88% acknowledged complementarity to conventional medicine. However, 24% found its definition unclear. Physician-patient communication remains challenging, with 48% of HCPs believing patients hesitate to discuss IO. Key needs include training (88%), standardized communication tools (45%), and a directory of recommended therapists (94%). The interviews facilitated a shift in perception, with 55% of HCPs expressing increased willingness to engage in IO initiatives.

Summary: Successfully integrating IO requires tailored training, specialized referents, and a well structured care pathway. The observed shift in mindset among HCPs highlights the importance of awareness and collaborative solution-building for effective IO adoption.

综述目的:综合肿瘤学(IO)已经发展成为一门由主要肿瘤组织认可的循证学科。然而,将IO纳入标准肿瘤治疗仍然是一个挑战,通常取决于机构文化和提供者的态度。本探索性试点研究旨在评估比利时综合癌症中心医疗保健专业人员(HCPs)的知识、沟通实践、感知需求和关于IO的观点,该中心没有预先存在的IO途径。最近的发现:在33名参与者中,45%的人认为IO是一种以患者为中心的方法,而88%的人认为IO是传统医学的补充。然而,24%的人认为其定义不明确。医患沟通仍然具有挑战性,48%的HCPs认为患者对讨论IO犹豫不决。主要需求包括培训(88%)、标准化沟通工具(45%)和推荐治疗师目录(94%)。访谈促进了观念的转变,55%的hcp表示更愿意参与IO计划。总结:成功整合IO需要量身定制的培训、专门的参考对象和结构良好的护理途径。在医疗保健提供者中观察到的思维转变突出了意识和协作解决方案构建对于有效采用IO的重要性。
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引用次数: 0
Are epigenetic-targeting approaches ready for prime time in neuroendocrine neoplasms? 表观遗传学靶向治疗神经内分泌肿瘤的时机准备好了吗?
IF 2.8 4区 医学 Q2 ONCOLOGY Pub Date : 2025-07-01 Epub Date: 2025-05-16 DOI: 10.1097/CCO.0000000000001158
Michel Meyers, Ioannis Karfis, Alain Hendlisz

Purpose of review: The purpose of this review is to evaluate the role of epigenetic-targeting approaches in the management of neuroendocrine neoplasms (NENs), particularly as a priming strategy for subsequent therapies. We explore the molecular basis of epigenetic modifications in NENs, and we review preclinical and clinical studies on DNA methyltransferase and histone deacetylase (HDAC) inhibitors.

Recent findings: DNA methyltransferase and HDAC inhibitors can upregulate SSTR2 expression, thereby improving radioligand uptake and treatment response in NENs. The LANTana study investigates ASTX727 as a strategy to restore SSTR2 expression in metastatic NENs, allowing previously ineligible patients to receive PRRT. Preclinical studies demonstrate that combining epigenetic agents with radiotherapy, chemotherapy, or targeted inhibitors can enhance tumour sensitivity and overcome resistance.

Summary: Epigenetic modifications play a crucial role in NENs, influencing tumour progression, therapy resistance, and SSTR2 expression. Epigenetic priming with DNA methyltransferase and HDAC inhibitors can enhance SSTR2 expression, improving the efficacy of PRRT in NENs. The LANTana study and other trials are investigating whether epigenetic-targeting approaches can be integrated into NEN treatment to optimize PRRT and overcome therapeutic limitations.

综述目的:本综述的目的是评估表观遗传学靶向方法在神经内分泌肿瘤(NENs)治疗中的作用,特别是作为后续治疗的启动策略。我们探讨了NENs表观遗传修饰的分子基础,并综述了DNA甲基转移酶和组蛋白去乙酰化酶(HDAC)抑制剂的临床前和临床研究。最近的研究发现:DNA甲基转移酶和HDAC抑制剂可以上调SSTR2的表达,从而改善NENs的放射配体摄取和治疗反应。LANTana研究调查了ASTX727作为恢复转移性NENs中SSTR2表达的策略,允许先前不合格的患者接受PRRT。临床前研究表明,将表观遗传药物与放疗、化疗或靶向抑制剂联合使用可以增强肿瘤敏感性并克服耐药性。摘要:表观遗传修饰在NENs中起关键作用,影响肿瘤进展、治疗耐药性和SSTR2表达。表观遗传启动DNA甲基转移酶和HDAC抑制剂可以增强SSTR2的表达,提高PRRT在NENs中的疗效。LANTana研究和其他试验正在研究表观遗传靶向方法是否可以整合到NEN治疗中,以优化PRRT并克服治疗局限性。
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引用次数: 0
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Current Opinion in Oncology
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