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Primary retroperitoneal choriocarcinoma with lung and liver metastasis in a male patient: case report 一名男性患者的原发性腹膜后绒毛膜癌伴肺和肝转移:病例报告
IF 0.9 4区 医学 Q4 Medicine Pub Date : 2024-01-03 DOI: 10.1515/oncologie-2023-0287
Guimei Wang, Ronghui Li
Abstract Objectives Non-gestational primary choriocarcinoma is an extremely rare malignant tumor with atypical clinical symptoms, especially in males. It usually occurs in the midline of the body, such as the mediastinum and retroperitoneum. Pathological diagnosis of primary retroperitoneal choriocarcinoma presents many challenges. More importantly, it is insensitive to therapy and has a poor prognosis. To date, there is still no standard treatment strategy for primary choriocarcinoma. Case presentation This case report presented a 27-year-old male with acute abdominal pain as the main symptom. And then, retroperitoneal choriocarcinoma with lung and liver metastasis was diagnosed. Palliative surgery was performed to alleviate the abdominal pain but complete tumor removal was not achieved. Subsequently, we gave the treatment with cytotoxic chemotherapy and immune checkpoint inhibitor blockade. The tumor was significantly reduced in size after six cycles of immunotherapy and chemotherapy, and also β-hCG level returned to normal. The tumor was not in complete remission, so penpulimab immuno-maintenance therapy was given. So far, the tumor control is stable, and the patient’s quality of life is also very well. Conclusions Pathological diagnosis of primary choriocarcinoma is very necessary, and the related molecular markers can assist. Immunotherapy combined with chemotherapy is effective in the treatment of primary retroperitoneal choriocarcinoma.
摘要 目的 非妊娠原发性绒毛膜癌是一种极为罕见的恶性肿瘤,临床症状不典型,尤其多见于男性。它通常发生在身体中线,如纵隔和腹膜后。原发性腹膜后绒毛膜癌的病理诊断面临许多挑战。更重要的是,它对治疗不敏感,预后较差。迄今为止,原发性绒毛膜癌仍没有标准的治疗策略。病例介绍 本病例报告的患者为一名 27 岁男性,主要症状为急性腹痛。随后确诊为腹膜后绒毛膜癌,并伴有肺和肝转移。我们进行了姑息手术以缓解腹痛,但未能完全切除肿瘤。随后,我们给予了细胞毒化疗和免疫检查点抑制剂阻断治疗。经过六个周期的免疫治疗和化疗,肿瘤明显缩小,β-hCG水平也恢复正常。由于肿瘤未完全缓解,患者接受了戊普利单抗免疫维持治疗。目前,肿瘤控制稳定,患者的生活质量也很好。结论 原发性绒毛膜癌的病理诊断非常必要,相关的分子标记物可以辅助诊断。免疫治疗联合化疗对原发性腹膜后绒毛膜癌的治疗是有效的。
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引用次数: 0
Primary retroperitoneal choriocarcinoma with lung and liver metastasis in a male patient: case report 一名男性患者的原发性腹膜后绒毛膜癌伴肺和肝转移:病例报告
IF 0.9 4区 医学 Q4 Medicine Pub Date : 2024-01-03 DOI: 10.1515/oncologie-2023-0287
Guimei Wang, Ronghui Li
Abstract Objectives Non-gestational primary choriocarcinoma is an extremely rare malignant tumor with atypical clinical symptoms, especially in males. It usually occurs in the midline of the body, such as the mediastinum and retroperitoneum. Pathological diagnosis of primary retroperitoneal choriocarcinoma presents many challenges. More importantly, it is insensitive to therapy and has a poor prognosis. To date, there is still no standard treatment strategy for primary choriocarcinoma. Case presentation This case report presented a 27-year-old male with acute abdominal pain as the main symptom. And then, retroperitoneal choriocarcinoma with lung and liver metastasis was diagnosed. Palliative surgery was performed to alleviate the abdominal pain but complete tumor removal was not achieved. Subsequently, we gave the treatment with cytotoxic chemotherapy and immune checkpoint inhibitor blockade. The tumor was significantly reduced in size after six cycles of immunotherapy and chemotherapy, and also β-hCG level returned to normal. The tumor was not in complete remission, so penpulimab immuno-maintenance therapy was given. So far, the tumor control is stable, and the patient’s quality of life is also very well. Conclusions Pathological diagnosis of primary choriocarcinoma is very necessary, and the related molecular markers can assist. Immunotherapy combined with chemotherapy is effective in the treatment of primary retroperitoneal choriocarcinoma.
摘要 目的 非妊娠原发性绒毛膜癌是一种极为罕见的恶性肿瘤,临床症状不典型,尤其多见于男性。它通常发生在身体中线,如纵隔和腹膜后。原发性腹膜后绒毛膜癌的病理诊断面临许多挑战。更重要的是,它对治疗不敏感,预后较差。迄今为止,原发性绒毛膜癌仍没有标准的治疗策略。病例介绍 本病例报告的患者为一名 27 岁男性,主要症状为急性腹痛。随后确诊为腹膜后绒毛膜癌,并伴有肺和肝转移。我们进行了姑息手术以缓解腹痛,但未能完全切除肿瘤。随后,我们给予了细胞毒化疗和免疫检查点抑制剂阻断治疗。经过六个周期的免疫治疗和化疗,肿瘤明显缩小,β-hCG水平也恢复正常。由于肿瘤未完全缓解,患者接受了戊普利单抗免疫维持治疗。目前,肿瘤控制稳定,患者的生活质量也很好。结论 原发性绒毛膜癌的病理诊断非常必要,相关的分子标记物可以辅助诊断。免疫治疗联合化疗对原发性腹膜后绒毛膜癌的治疗是有效的。
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引用次数: 0
Primary retroperitoneal choriocarcinoma with lung and liver metastasis in a male patient: case report 一名男性患者的原发性腹膜后绒毛膜癌伴肺和肝转移:病例报告
IF 0.9 4区 医学 Q4 Medicine Pub Date : 2024-01-03 DOI: 10.1515/oncologie-2023-0287
Guimei Wang, Ronghui Li
Abstract Objectives Non-gestational primary choriocarcinoma is an extremely rare malignant tumor with atypical clinical symptoms, especially in males. It usually occurs in the midline of the body, such as the mediastinum and retroperitoneum. Pathological diagnosis of primary retroperitoneal choriocarcinoma presents many challenges. More importantly, it is insensitive to therapy and has a poor prognosis. To date, there is still no standard treatment strategy for primary choriocarcinoma. Case presentation This case report presented a 27-year-old male with acute abdominal pain as the main symptom. And then, retroperitoneal choriocarcinoma with lung and liver metastasis was diagnosed. Palliative surgery was performed to alleviate the abdominal pain but complete tumor removal was not achieved. Subsequently, we gave the treatment with cytotoxic chemotherapy and immune checkpoint inhibitor blockade. The tumor was significantly reduced in size after six cycles of immunotherapy and chemotherapy, and also β-hCG level returned to normal. The tumor was not in complete remission, so penpulimab immuno-maintenance therapy was given. So far, the tumor control is stable, and the patient’s quality of life is also very well. Conclusions Pathological diagnosis of primary choriocarcinoma is very necessary, and the related molecular markers can assist. Immunotherapy combined with chemotherapy is effective in the treatment of primary retroperitoneal choriocarcinoma.
摘要 目的 非妊娠原发性绒毛膜癌是一种极为罕见的恶性肿瘤,临床症状不典型,尤其多见于男性。它通常发生在身体中线,如纵隔和腹膜后。原发性腹膜后绒毛膜癌的病理诊断面临许多挑战。更重要的是,它对治疗不敏感,预后较差。迄今为止,原发性绒毛膜癌仍没有标准的治疗策略。病例介绍 本病例报告的患者为一名 27 岁男性,主要症状为急性腹痛。随后确诊为腹膜后绒毛膜癌,并伴有肺和肝转移。我们进行了姑息手术以缓解腹痛,但未能完全切除肿瘤。随后,我们给予了细胞毒化疗和免疫检查点抑制剂阻断治疗。经过六个周期的免疫治疗和化疗,肿瘤明显缩小,β-hCG水平也恢复正常。由于肿瘤未完全缓解,患者接受了戊普利单抗免疫维持治疗。目前,肿瘤控制稳定,患者的生活质量也很好。结论 原发性绒毛膜癌的病理诊断非常必要,相关的分子标记物可以辅助诊断。免疫治疗联合化疗对原发性腹膜后绒毛膜癌的治疗是有效的。
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引用次数: 0
The tumor microenvironment: a key player in multidrug resistance in cancer 肿瘤微环境:癌症多药耐药性的关键因素
IF 0.9 4区 医学 Q4 Medicine Pub Date : 2024-01-03 DOI: 10.1515/oncologie-2023-0459
Lingnan Meng, Ying Zheng, Hao Liu, Daiming Fan
Abstract Cancer is the second leading cause of death worldwide. Although multiple new cancer treatments have emerged in recent years, drug therapy, mainly comprising chemotherapy, targeted therapy, and immunotherapy, remains the most common approach. The multidrug resistance (MDR) of cancer cells to various treatments remains a challenge. Scientists have always focused on the acquired drug resistance mechanisms of tumor cells themselves. However, recent evidence shows that the tumor microenvironment (TME) plays a critical role in regulating tumor cell progression, metastasis, immune escape, and drug resistance. In the TME, interactions between cancer cells and non-malignant cells often modify the TME and facilitate drug resistance. Therefore, elucidating this complex interaction mechanism is essential for the development of effective treatments. This review focuses on the role of the TME in promoting chemoresistance in tumor cells through the following mechanisms: (i) inhibiting the immune clearance of tumor cells and facilitating immune escape responses; (ii) stimulating the release of soluble paracrine factors to enhance tumor survival and growth; (iii) promoting survival and altering drug delivery through metabolic reprogramming; (iv) obstructing drug absorption by inducing changes in stomatal cells and blood vessels surrounding the tumor; and (v) inducing the cancer stem cell phenotype. This review also addresses a clinical treatment strategy for targeting the TME, providing insights and a basis for reversing multidrug resistance.
摘要 癌症是全球第二大死因。尽管近年来出现了多种新的癌症治疗方法,但药物治疗(主要包括化疗、靶向治疗和免疫治疗)仍是最常用的方法。癌细胞对各种疗法的多药耐药性(MDR)仍然是一个挑战。科学家们一直关注肿瘤细胞本身的获得性耐药机制。然而,最近的证据表明,肿瘤微环境(TME)在调控肿瘤细胞进展、转移、免疫逃逸和耐药性方面起着至关重要的作用。在肿瘤微环境中,癌细胞与非恶性细胞之间的相互作用往往会改变肿瘤微环境并促进耐药性的产生。因此,阐明这种复杂的相互作用机制对于开发有效的治疗方法至关重要。本综述重点探讨TME通过以下机制促进肿瘤细胞产生化疗耐药性的作用:(i) 抑制肿瘤细胞的免疫清除,促进免疫逃逸反应;(ii) 刺激可溶性旁分泌因子的释放,增强肿瘤的生存和生长;(iii) 通过代谢重编程促进生存和改变药物输送;(iv) 通过诱导肿瘤周围气孔细胞和血管的变化阻碍药物吸收;(v) 诱导癌症干细胞表型。本综述还探讨了针对TME的临床治疗策略,为逆转多药耐药性提供了见解和依据。
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引用次数: 0
The tumor microenvironment: a key player in multidrug resistance in cancer 肿瘤微环境:癌症多药耐药性的关键因素
IF 0.9 4区 医学 Q4 Medicine Pub Date : 2024-01-03 DOI: 10.1515/oncologie-2023-0459
Lingnan Meng, Ying Zheng, Hao Liu, Daiming Fan
Abstract Cancer is the second leading cause of death worldwide. Although multiple new cancer treatments have emerged in recent years, drug therapy, mainly comprising chemotherapy, targeted therapy, and immunotherapy, remains the most common approach. The multidrug resistance (MDR) of cancer cells to various treatments remains a challenge. Scientists have always focused on the acquired drug resistance mechanisms of tumor cells themselves. However, recent evidence shows that the tumor microenvironment (TME) plays a critical role in regulating tumor cell progression, metastasis, immune escape, and drug resistance. In the TME, interactions between cancer cells and non-malignant cells often modify the TME and facilitate drug resistance. Therefore, elucidating this complex interaction mechanism is essential for the development of effective treatments. This review focuses on the role of the TME in promoting chemoresistance in tumor cells through the following mechanisms: (i) inhibiting the immune clearance of tumor cells and facilitating immune escape responses; (ii) stimulating the release of soluble paracrine factors to enhance tumor survival and growth; (iii) promoting survival and altering drug delivery through metabolic reprogramming; (iv) obstructing drug absorption by inducing changes in stomatal cells and blood vessels surrounding the tumor; and (v) inducing the cancer stem cell phenotype. This review also addresses a clinical treatment strategy for targeting the TME, providing insights and a basis for reversing multidrug resistance.
摘要 癌症是全球第二大死因。尽管近年来出现了多种新的癌症治疗方法,但药物治疗(主要包括化疗、靶向治疗和免疫治疗)仍是最常用的方法。癌细胞对各种疗法的多药耐药性(MDR)仍然是一个挑战。科学家们一直关注肿瘤细胞本身的获得性耐药机制。然而,最近的证据表明,肿瘤微环境(TME)在调控肿瘤细胞进展、转移、免疫逃逸和耐药性方面起着至关重要的作用。在肿瘤微环境中,癌细胞与非恶性细胞之间的相互作用往往会改变肿瘤微环境并促进耐药性的产生。因此,阐明这种复杂的相互作用机制对于开发有效的治疗方法至关重要。本综述重点探讨TME通过以下机制促进肿瘤细胞产生化疗耐药性的作用:(i) 抑制肿瘤细胞的免疫清除,促进免疫逃逸反应;(ii) 刺激可溶性旁分泌因子的释放,增强肿瘤的生存和生长;(iii) 通过代谢重编程促进生存和改变药物输送;(iv) 通过诱导肿瘤周围气孔细胞和血管的变化阻碍药物吸收;(v) 诱导癌症干细胞表型。本综述还探讨了针对TME的临床治疗策略,为逆转多药耐药性提供了见解和依据。
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引用次数: 0
Disulfidptosis-related long non-coding RNAs predict prognosis and indicate therapeutic response in non-small cell lung carcinoma 与脱硫相关的长非编码 RNA 可预测非小细胞肺癌的预后并显示治疗反应
IF 0.9 4区 医学 Q4 Medicine Pub Date : 2024-01-03 DOI: 10.1515/oncologie-2023-0384
Huan Liu, Shaohua He, L. Tan, Mingzhen Li, Cheng Chen, Ruiming Tan
Abstract Objectives Disulfidptosis is a novel form of cell death, whose modulation in tumor cells may present a promising therapeutic strategy for cancer treatment. However, the role of disulfidptosis-related long non-coding RNAs (lncRNAs) in non-small cell lung carcinoma (NSCLC) remains poorly elucidated. This study aims to investigate the prognostic significance of disulfidptosis-related lncRNAs (DRLs) and reveal their relationship to the immune microenvironment of NSCLC. Methods DRLs were identified through co-expression analysis of NSCLC transcriptomic data obtained from the Genomic Data Commons (GDC) data portal. The DRLs prognostic signature (DRLPS) was established using the least absolute shrinkage and selection operator (LASSO) and Cox regression analyses. Samples were separated into high-DS and low-DS groups based on the median disulfidptosis score (DS) of DRLPS. Integrated analyses were then implemented to unveil the association between DRLs and NSCLC microenvironment. These involved the evaluation of functional enrichments, immune cell infiltrations, genetic alterations, and drug sensitivity. Results A prognostic signature was developed based on six prognostic DRLs, which are AL606489.1, LINC00857, AP003555.1, AP000695.1, AC113346.1, and LINC01615. The Kaplan–Meier survival curves demonstrated the significant association between DRLPS and NSCLC prognosis. The functional enrichment assessment revealed the pivotal involvement of DRLs in immune regulation and metabolism in NSCLC. The low-DS and high-DS subgroups of NSCLC patients exhibited distinct differences in terms of immune infiltration and tumor mutation burden. The potential to predict immunotherapy benefit and drug sensitivity in NSCLC treatments was observed in DRLPS. Conclusions In this study, disulfidptosis-related lncRNAs were identified and their roles in NSCLC were revealed. A novel prognostic signature with the potential to predict drug response in NSCLC treatment was developed.
摘要 目的 二硫化硫是一种新型的细胞死亡形式,在肿瘤细胞中对其进行调节可能是一种很有前景的癌症治疗策略。然而,与二硫化相关的长非编码 RNA(lncRNA)在非小细胞肺癌(NSCLC)中的作用仍未得到充分阐明。本研究旨在探讨二硫化相关lncRNAs(DRLs)的预后意义,并揭示它们与NSCLC免疫微环境的关系。方法 通过对基因组数据公共平台(GDC)数据门户获取的NSCLC转录组数据进行共表达分析,确定DRLs。使用最小绝对收缩和选择算子(LASSO)和 Cox 回归分析建立了 DRLs 预后特征(DRLPS)。根据DRLPS的中位二硫化硫评分(DS),将样本分为高DS组和低DS组。然后进行综合分析,以揭示 DRLs 与 NSCLC 微环境之间的关联。其中包括对功能富集、免疫细胞浸润、基因改变和药物敏感性的评估。结果 基于六个预后DRLs,即AL606489.1、LINC00857、AP003555.1、AP000695.1、AC113346.1和LINC01615,建立了一个预后特征。Kaplan-Meier生存曲线显示了DRLPS与NSCLC预后的显著相关性。功能富集评估显示,DRLs在NSCLC的免疫调节和新陈代谢中起着关键作用。NSCLC患者中的低DRLPS亚组和高DRLPS亚组在免疫浸润和肿瘤突变负荷方面表现出明显的差异。在 DRLPS 中观察到了预测 NSCLC 治疗中免疫疗法获益和药物敏感性的潜力。结论 本研究发现了与二硫化相关的 lncRNAs,并揭示了它们在 NSCLC 中的作用。研究还发现了一种新的预后特征,该特征具有预测 NSCLC 治疗中药物反应的潜力。
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引用次数: 0
The tumor microenvironment: a key player in multidrug resistance in cancer 肿瘤微环境:癌症多药耐药性的关键因素
IF 0.9 4区 医学 Q4 Medicine Pub Date : 2024-01-03 DOI: 10.1515/oncologie-2023-0459
Lingnan Meng, Ying Zheng, Hao Liu, Daiming Fan
Abstract Cancer is the second leading cause of death worldwide. Although multiple new cancer treatments have emerged in recent years, drug therapy, mainly comprising chemotherapy, targeted therapy, and immunotherapy, remains the most common approach. The multidrug resistance (MDR) of cancer cells to various treatments remains a challenge. Scientists have always focused on the acquired drug resistance mechanisms of tumor cells themselves. However, recent evidence shows that the tumor microenvironment (TME) plays a critical role in regulating tumor cell progression, metastasis, immune escape, and drug resistance. In the TME, interactions between cancer cells and non-malignant cells often modify the TME and facilitate drug resistance. Therefore, elucidating this complex interaction mechanism is essential for the development of effective treatments. This review focuses on the role of the TME in promoting chemoresistance in tumor cells through the following mechanisms: (i) inhibiting the immune clearance of tumor cells and facilitating immune escape responses; (ii) stimulating the release of soluble paracrine factors to enhance tumor survival and growth; (iii) promoting survival and altering drug delivery through metabolic reprogramming; (iv) obstructing drug absorption by inducing changes in stomatal cells and blood vessels surrounding the tumor; and (v) inducing the cancer stem cell phenotype. This review also addresses a clinical treatment strategy for targeting the TME, providing insights and a basis for reversing multidrug resistance.
摘要 癌症是全球第二大死因。尽管近年来出现了多种新的癌症治疗方法,但药物治疗(主要包括化疗、靶向治疗和免疫治疗)仍是最常用的方法。癌细胞对各种疗法的多药耐药性(MDR)仍然是一个挑战。科学家们一直关注肿瘤细胞本身的获得性耐药机制。然而,最近的证据表明,肿瘤微环境(TME)在调控肿瘤细胞进展、转移、免疫逃逸和耐药性方面起着至关重要的作用。在肿瘤微环境中,癌细胞与非恶性细胞之间的相互作用往往会改变肿瘤微环境并促进耐药性的产生。因此,阐明这种复杂的相互作用机制对于开发有效的治疗方法至关重要。本综述重点探讨TME通过以下机制促进肿瘤细胞产生化疗耐药性的作用:(i) 抑制肿瘤细胞的免疫清除,促进免疫逃逸反应;(ii) 刺激可溶性旁分泌因子的释放,增强肿瘤的生存和生长;(iii) 通过代谢重编程促进生存和改变药物输送;(iv) 通过诱导肿瘤周围气孔细胞和血管的变化阻碍药物吸收;(v) 诱导癌症干细胞表型。本综述还探讨了针对TME的临床治疗策略,为逆转多药耐药性提供了见解和依据。
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引用次数: 0
Immunotherapy in hepatocellular carcinoma: an overview of immune checkpoint inhibitors, drug resistance, and adverse effects 肝细胞癌的免疫疗法:免疫检查点抑制剂、耐药性和不良反应概述
IF 0.9 4区 医学 Q4 Medicine Pub Date : 2024-01-03 DOI: 10.1515/oncologie-2023-0412
Xuan-Yu Gu, Jin-Long Huo, Zhi-Yong Yu, Ji-Chang Jiang, Ya-Xuan Xu, Lijin Zhao
Abstract Hepatocellular carcinoma (HCC) is a concerning liver cancer with rising incidence and mortality rates worldwide. The effectiveness of traditional therapies in managing advanced HCC is limited, necessitating the development of new therapeutic strategies. Immune checkpoint inhibitors (ICIs) have emerged as a promising strategy for HCC management. By preventing tumor cells from evading immune surveillance through immunological checkpoints, ICIs can restore the immune system’s ability to target and eliminate tumors. While ICIs show promise in enhancing the immune response against malignancies, challenges such as drug resistance and adverse reactions hinder their efficacy. To address these challenges, developing individualized ICI treatment strategies is critical. Combining targeted therapy and immunotherapy holds the potential for comprehensive therapeutic effects. Additionally, biomarker-based individualized ICI treatment strategies offer promise in predicting treatment response and guiding personalized patient care. Future research should explore emerging ICI treatment methods to optimize HCC immunotherapy. This review provides an overview of ICIs as a new treatment for HCC, demonstrating some success in promoting the tumor immune response. However, drug resistance and adverse reactions remain important considerations that must be addressed. As tailored treatment plans evolve, the prospect of immunotherapy for HCC is expected to grow, offering new opportunities for improved patient outcomes.
摘要 肝细胞癌(HCC)是一种令人担忧的肝癌,其发病率和死亡率在全球不断上升。传统疗法对晚期肝细胞癌的治疗效果有限,因此有必要开发新的治疗策略。免疫检查点抑制剂(ICIs)已成为一种很有前景的HCC治疗策略。通过免疫检查点阻止肿瘤细胞逃避免疫监视,ICIs 可以恢复免疫系统靶向和消灭肿瘤的能力。虽然 ICIs 有望增强针对恶性肿瘤的免疫反应,但耐药性和不良反应等挑战阻碍了 ICIs 的疗效。为了应对这些挑战,制定个体化的 ICI 治疗策略至关重要。将靶向治疗与免疫治疗相结合,有可能产生全面的治疗效果。此外,基于生物标志物的个体化 ICI 治疗策略有望预测治疗反应并指导个性化患者护理。未来的研究应探索新兴的 ICI 治疗方法,以优化 HCC 免疫疗法。本综述概述了 ICIs 作为 HCC 新疗法的情况,显示其在促进肿瘤免疫反应方面取得了一些成功。然而,耐药性和不良反应仍然是必须解决的重要问题。随着量身定制的治疗方案不断发展,HCC 免疫疗法的前景有望扩大,为改善患者预后提供了新的机遇。
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引用次数: 0
Primary retroperitoneal choriocarcinoma with lung and liver metastasis in a male patient: case report 一名男性患者的原发性腹膜后绒毛膜癌伴肺和肝转移:病例报告
IF 0.9 4区 医学 Q4 Medicine Pub Date : 2024-01-03 DOI: 10.1515/oncologie-2023-0287
Guimei Wang, Ronghui Li
Abstract Objectives Non-gestational primary choriocarcinoma is an extremely rare malignant tumor with atypical clinical symptoms, especially in males. It usually occurs in the midline of the body, such as the mediastinum and retroperitoneum. Pathological diagnosis of primary retroperitoneal choriocarcinoma presents many challenges. More importantly, it is insensitive to therapy and has a poor prognosis. To date, there is still no standard treatment strategy for primary choriocarcinoma. Case presentation This case report presented a 27-year-old male with acute abdominal pain as the main symptom. And then, retroperitoneal choriocarcinoma with lung and liver metastasis was diagnosed. Palliative surgery was performed to alleviate the abdominal pain but complete tumor removal was not achieved. Subsequently, we gave the treatment with cytotoxic chemotherapy and immune checkpoint inhibitor blockade. The tumor was significantly reduced in size after six cycles of immunotherapy and chemotherapy, and also β-hCG level returned to normal. The tumor was not in complete remission, so penpulimab immuno-maintenance therapy was given. So far, the tumor control is stable, and the patient’s quality of life is also very well. Conclusions Pathological diagnosis of primary choriocarcinoma is very necessary, and the related molecular markers can assist. Immunotherapy combined with chemotherapy is effective in the treatment of primary retroperitoneal choriocarcinoma.
摘要 目的 非妊娠原发性绒毛膜癌是一种极为罕见的恶性肿瘤,临床症状不典型,尤其多见于男性。它通常发生在身体中线,如纵隔和腹膜后。原发性腹膜后绒毛膜癌的病理诊断面临许多挑战。更重要的是,它对治疗不敏感,预后较差。迄今为止,原发性绒毛膜癌仍没有标准的治疗策略。病例介绍 本病例报告的患者为一名 27 岁男性,主要症状为急性腹痛。随后确诊为腹膜后绒毛膜癌,并伴有肺和肝转移。我们进行了姑息手术以缓解腹痛,但未能完全切除肿瘤。随后,我们给予了细胞毒化疗和免疫检查点抑制剂阻断治疗。经过六个周期的免疫治疗和化疗,肿瘤明显缩小,β-hCG水平也恢复正常。由于肿瘤没有完全缓解,因此患者接受了 Penpulimab 免疫维持治疗。目前,肿瘤控制稳定,患者的生活质量也很好。结论 原发性绒毛膜癌的病理诊断非常必要,相关的分子标记物可以辅助诊断。免疫治疗联合化疗对原发性腹膜后绒毛膜癌的治疗是有效的。
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引用次数: 0
Disulfidptosis-related long non-coding RNAs predict prognosis and indicate therapeutic response in non-small cell lung carcinoma 与脱硫相关的长非编码 RNA 可预测非小细胞肺癌的预后并显示治疗反应
IF 0.9 4区 医学 Q4 Medicine Pub Date : 2024-01-03 DOI: 10.1515/oncologie-2023-0384
Huan Liu, Shaohua He, L. Tan, Mingzhen Li, Cheng Chen, Ruiming Tan
Abstract Objectives Disulfidptosis is a novel form of cell death, whose modulation in tumor cells may present a promising therapeutic strategy for cancer treatment. However, the role of disulfidptosis-related long non-coding RNAs (lncRNAs) in non-small cell lung carcinoma (NSCLC) remains poorly elucidated. This study aims to investigate the prognostic significance of disulfidptosis-related lncRNAs (DRLs) and reveal their relationship to the immune microenvironment of NSCLC. Methods DRLs were identified through co-expression analysis of NSCLC transcriptomic data obtained from the Genomic Data Commons (GDC) data portal. The DRLs prognostic signature (DRLPS) was established using the least absolute shrinkage and selection operator (LASSO) and Cox regression analyses. Samples were separated into high-DS and low-DS groups based on the median disulfidptosis score (DS) of DRLPS. Integrated analyses were then implemented to unveil the association between DRLs and NSCLC microenvironment. These involved the evaluation of functional enrichments, immune cell infiltrations, genetic alterations, and drug sensitivity. Results A prognostic signature was developed based on six prognostic DRLs, which are AL606489.1, LINC00857, AP003555.1, AP000695.1, AC113346.1, and LINC01615. The Kaplan–Meier survival curves demonstrated the significant association between DRLPS and NSCLC prognosis. The functional enrichment assessment revealed the pivotal involvement of DRLs in immune regulation and metabolism in NSCLC. The low-DS and high-DS subgroups of NSCLC patients exhibited distinct differences in terms of immune infiltration and tumor mutation burden. The potential to predict immunotherapy benefit and drug sensitivity in NSCLC treatments was observed in DRLPS. Conclusions In this study, disulfidptosis-related lncRNAs were identified and their roles in NSCLC were revealed. A novel prognostic signature with the potential to predict drug response in NSCLC treatment was developed.
摘要 目的 二硫化硫是一种新型的细胞死亡形式,在肿瘤细胞中对其进行调节可能是一种很有前景的癌症治疗策略。然而,与二硫化相关的长非编码 RNA(lncRNA)在非小细胞肺癌(NSCLC)中的作用仍未得到充分阐明。本研究旨在探讨二硫化相关lncRNAs(DRLs)的预后意义,并揭示它们与NSCLC免疫微环境的关系。方法 通过对基因组数据公共平台(GDC)数据门户获取的NSCLC转录组数据进行共表达分析,确定DRLs。使用最小绝对收缩和选择算子(LASSO)和 Cox 回归分析建立了 DRLs 预后特征(DRLPS)。根据DRLPS的中位二硫化硫评分(DS),将样本分为高DS组和低DS组。然后进行综合分析,以揭示 DRLs 与 NSCLC 微环境之间的关联。其中包括对功能富集、免疫细胞浸润、基因改变和药物敏感性的评估。结果 基于六个预后DRLs,即AL606489.1、LINC00857、AP003555.1、AP000695.1、AC113346.1和LINC01615,建立了一个预后特征。Kaplan-Meier生存曲线显示了DRLPS与NSCLC预后的显著相关性。功能富集评估显示,DRLs在NSCLC的免疫调节和新陈代谢中起着关键作用。NSCLC患者中的低DRLPS亚组和高DRLPS亚组在免疫浸润和肿瘤突变负荷方面表现出明显的差异。在 DRLPS 中观察到了预测 NSCLC 治疗中免疫疗法获益和药物敏感性的潜力。结论 本研究发现了与二硫化相关的 lncRNAs,并揭示了它们在 NSCLC 中的作用。研究还发现了一种新的预后特征,该特征具有预测 NSCLC 治疗中药物反应的潜力。
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Oncologie
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