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Cancer care in Needle Hospital, Hargeisa, Somaliland 索马里兰哈尔格萨针医院的癌症护理
Pub Date : 2023-11-30 DOI: 10.3332/ecancer.2023.1642
Gebrekirstos Hagos, Nazik Hammad, Susannah Stanway, A. Yusuf, Tekleberhan Hailemariam
Somaliland is an autonomous region in the northern part of Somalia that declared its independence in 1991. It is a low-income country (LIC) with a population size of 5.7 million with a gross domestic product per capita of $775. Health services are delivered by public, private and non-governmental organisations. The public health care system in Somaliland is facing huge challenges. Seven percent of the population suffers from non-communicable diseases, but data on cancer incidence and mortality are not available. Much of the emphasis in public health has been placed on primary care and maternal and child health. There is still a large gap in cancer prevention, early detection and screening in the country. Additionally, there is no cancer registry or published data on cancer. Currently, there are a few private hospitals that provide chemotherapy services in Somaliland of which Needle Hospital is one. Services provided in this hospital include medical oncology for all solid tumours, palliative care, follow-up and cancer health education. The hospital provides services for patients from Somaliland and neighbouring countries including Djibouti, Somalia and Ethiopia. As a new oncology clinic in an LIC, the clinic is facing many challenges, like the absence of a multidisciplinary tumour board, presentation of patients at the advanced stage of tumours and poor cancer awareness in the general population.
索马里兰是索马里北部的一个自治区,于 1991 年宣布独立。它是一个低收入国家(LIC),人口为 570 万,人均国内生产总值为 775 美元。医疗服务由公共、私营和非政府组织提供。索马里兰的公共医疗保健系统正面临着巨大的挑战。7%的人口患有非传染性疾病,但没有癌症发病率和死亡率的数据。公共卫生的重点主要放在初级保健和妇幼保健上。该国在癌症预防、早期检测和筛查方面仍存在巨大差距。此外,也没有癌症登记册或公布的癌症数据。目前,索马里兰有几家私立医院提供化疗服务,Needle 医院就是其中之一。该医院提供的服务包括所有实体瘤的肿瘤内科治疗、姑息治疗、后续治疗和癌症健康教育。医院为来自索马里兰以及吉布提、索马里和埃塞俄比亚等邻国的病人提供服务。作为一个位于低收入国家的新肿瘤诊所,该诊所面临着许多挑战,如缺乏多学科肿瘤委员会、病人处于肿瘤晚期以及普通民众对癌症认识不足等。
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引用次数: 0
Successful long-term management of metastatic clear cell renal cell carcinoma with nivolumab: a case report and literature review 尼妥珠单抗对转移性透明细胞肾细胞癌的长期成功治疗:病例报告和文献综述
Pub Date : 2023-11-30 DOI: 10.3332/ecancer.2023.1643
Nicolás Duque Clavijo, Paula A Lara, John Alejandro Murillo Silva, I. Triana, H. A. Vargas, Luis Eduardo Pino, Javier Mauricio Segovia, Erick Andrés Cantor
In Colombia, renal cancer is a rare condition, with clear cell renal cell carcinoma (ccRCC) being the most prevalent neoplasm. In recent years, immune checkpoint inhibitors (ICI) have been proposed for the management of metastatic disease, as they have shown improved rates of response and long-term survival. Furthermore, they exhibit a favourable tolerance profile, and adverse events causing significant morbidity are infrequent. We report the case of a 61-year-old male patient initially diagnosed with early-stage ccRCC who underwent right nephrectomy in 2009. Six years later, disease recurrence with metastatic compromise was documented, which led to the resection of the L1 vertebral body followed by radiotherapy and maintenance treatment with sunitinib. Due to disease progression, treatment with sunitinib was discontinued. Subsequently, evero-limus was initiated as second-line immunotherapy, which was later discontinued due to the appearance of new metastatic lesions. In 2017, the patient was referred to our institution, where a third-line pharmacological treatment with nivolumab was initiated. In 2022, complete remission by positron emission tomography-computed tomography (PET-CT) was evidenced, which has been sustained to date. This case demonstrates the efficacy and safety of ICI in patients with metastatic ccRCC. The case presented is relevant in that it describes the achievement of complete remission in a patient who did not respond to the first two lines of immunotherapy. Given the limited literature regarding the discontinuation of therapy after achieving sustained remission, further research is warranted to explore this topic.
在哥伦比亚,肾癌是一种罕见疾病,其中透明细胞肾细胞癌(ccRCC)是最常见的肿瘤。近年来,免疫检查点抑制剂(ICI)被提议用于转移性疾病的治疗,因为它们显示出更高的反应率和长期生存率。此外,它们还表现出良好的耐受性,导致严重发病的不良反应也不常见。我们报告了一名 61 岁男性患者的病例,他最初被诊断为早期 ccRCC,于 2009 年接受了右肾切除术。六年后,疾病复发并出现转移性损害,因此患者接受了 L1 椎体切除术,随后接受放疗和舒尼替尼维持治疗。由于疾病进展,患者停止了舒尼替尼治疗。随后,开始使用依维莫司作为二线免疫疗法,后因出现新的转移病灶而停止。2017年,患者转诊至我院,开始接受尼妥珠单抗的三线药物治疗。2022 年,正电子发射计算机断层扫描(PET-CT)显示患者病情完全缓解,并持续至今。本病例证明了 ICI 对转移性 ccRCC 患者的有效性和安全性。本病例的相关性在于,它描述了一位对前两种免疫疗法均无反应的患者实现了完全缓解。鉴于有关患者在获得持续缓解后停止治疗的文献有限,我们有必要进一步研究探讨这一课题。
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引用次数: 0
The expression of VEGF and cyclin D1/EGFR in common primary liver carcinomas in Egypt: an immunohistochemical study 埃及常见原发性肝癌中血管内皮生长因子和细胞周期蛋白 D1/EGFR 的表达:一项免疫组化研究
Pub Date : 2023-11-27 DOI: 10.3332/ecancer.2023.1641
D. Sweed, Shaymaa Sabry El Gammal, S. Kilany, S. Abdelsattar, Sara Mohamed Abd Elhamed
Background: The most common types of primary malignant liver tumours are hepato-cellular carcinoma (HCC) and cholangiocarcinoma (CCA). Treatment options for patients who are inoperable/advanced, or recurring are challenging. Cyclin D1, epidermal growth factor (EGFR) and vascular endothelial growth factor (VEGR) are common carcinogenic proteins that have potential therapeutic targets in various cancers. They have been implicated in the development of HCC and CCA. In this study, we aimed to evaluate the oncogenic function expression of cyclin D1, EGFR and VEGF in HCC and CCA of Egyptian patients. This could help to validate their therapeutic potential. Material and methods: Tumour cases were selected from 82 cases of primary liver carcinomas, with 58 cases being from HCC and 24 cases from CCA compared to 51 non-tumour adjacent liver cases and 18 from normal liver tissue. The immunohistochemical study of cyclin D1, EGFR and VEGR was conducted. Results: Cyclin D1, EGFR and VEGF are overexpressed in HCC and CCA as compared to the control group ( p < 0.001). Cyclin D1 was related to well-differentiated grade and early pathologic stage in HCC ( p = 0.016 and p = 0.042, respectively). The well-differentiated grade showed significantly higher VEGF levels ( p = 0.04). In the CCA group, however, EGFR was strongly related to high tumour size ( p = 0.047). EGFR and VEGF were over-expressed in HCC raised in the non-cirrhotic liver compared to those developed in post-hepatitic liver cirrhosis ( p = 0.003 and p = 0.014). Conclusion: Cyclin D1, EGFR and VEGF shared significant overexpression in HCC and CCA. EGFR and VEGF may play an oncogenic function in the development of HCC in non-cirrhotic liver. Furthermore, cyclin D1 and VEGF may play a good prognostic function in HCC, but EGFR may play a bad prognostic role in CCA.
背景:最常见的原发性恶性肝肿瘤是肝细胞癌(HCC)和胆管癌(CCA)。无法手术/晚期或复发患者的治疗方案具有挑战性。细胞周期蛋白 D1、表皮生长因子(EGFR)和血管内皮生长因子(VEGR)是常见的致癌蛋白,是各种癌症的潜在治疗靶点。它们被认为与 HCC 和 CCA 的发展有关。本研究旨在评估细胞周期蛋白 D1、表皮生长因子受体和血管内皮生长因子在埃及 HCC 和 CCA 患者中的致癌功能表达。这有助于验证它们的治疗潜力。材料和方法:肿瘤病例选自 82 例原发性肝癌,其中 58 例来自 HCC,24 例来自 CCA,而非肿瘤邻近肝脏病例 51 例,正常肝组织 18 例。对细胞周期蛋白 D1、表皮生长因子受体(EGFR)和血管内皮生长因子受体(VEGR)进行免疫组化研究。结果显示与对照组相比,细胞周期蛋白 D1、表皮生长因子受体(EGFR)和血管内皮生长因子(VEGF)在 HCC 和 CCA 中过表达(P < 0.001)。细胞周期蛋白 D1 与 HCC 的分化程度和早期病理分期有关(分别为 p = 0.016 和 p = 0.042)。分化良好的分级显示血管内皮生长因子水平明显更高(p = 0.04)。然而,在CCA组中,表皮生长因子受体(EGFR)与肿瘤大小密切相关(p = 0.047)。与肝硬化后发生的 HCC 相比,非肝硬化发生的 HCC 表皮生长因子受体和血管内皮生长因子表达过高 ( p = 0.003 和 p = 0.014)。结论细胞周期蛋白 D1、表皮生长因子受体(EGFR)和血管内皮生长因子(VEGF)在 HCC 和 CCA 中均显著过表达。表皮生长因子受体(EGFR)和血管内皮生长因子(VEGF)可能在非肝硬化的 HCC 发病过程中发挥致癌作用。此外,细胞周期蛋白 D1 和血管内皮生长因子在 HCC 中可能起到良好的预后作用,但表皮生长因子受体在 CCA 中可能起到不良的预后作用。
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引用次数: 0
Activity of capecitabine for central nervous system metastases from breast cancer 卡培他滨对乳腺癌中枢神经系统转移的疗效
Pub Date : 2023-11-23 DOI: 10.3332/ecancer.2023.1638
Mariana Carvalho Gouveia, Cassio Murilo Trovo Hidalgo Filho, Raquel Andrade Moreno, Heitor Castelo Branco Rodrigues Alves, Aline Sgnolf Ayres, Laura Testa, Renata Colombo Bonadio
Purpose: Central nervous system (CNS) metastases are a significant burden in breast cancer (BC). Capecitabine is a frequent choice in this scenario, but data supporting its single-agent activity are scarce. We aimed to evaluate the intracranial efficacy of capecitabine in CNS metastases from BC. Methods: This retrospective cohort included patients with CNS metastases from BC treated with capecitabine at a single centre. Study endpoints were intracranial CNS objective response rate (CNS-ORR), intracranial CNS disease control rate (CNS-DCR), intracranial CNS progression-free survival (CNS-PFS) and overall survival (OS). Results: 209 patients were included; 41.6% hormone receptor-positive HER2-negative (HR + HER2-), 33.9% human epidermal growth factor receptor 2 positive (HER2+), and 26.4% triple-negative breast cancer (TNBC). Radiotherapy was performed in 90.4% and CNS surgery in 27.5%. Among patients accessible for intracranial response, 3-month CNS-ORR and CNS-DCR were 41.6% and 81.2%. CNS-ORR was numerically higher among TNBC (61% versus 38% in HR + HER2-BC and 35% in HER2 + BC) ( p = 0.194). When considering patients who were not evaluable at 3-month as non-responders, the 3-month CNS-ORR was 19.1% (18.4% in HR + HER2, 18.3% in HER2+, and 21.6% in TNBC). Nevertheless, TNBC was associated with lower CNS-PFS ( p < 0.001) and OS ( p < 0.001). Median PFS was 8.3 months in HR + HER2, 5.0 months in HER2+, and 3.0 months in TNBC. Median OS was 8.7, 9.1 and 4.5 months, respectively. Conclusion: Among patients with BC and CNS metastases accessible for intracranial response at 3 months, intracranial activity was observed with capecitabine. These patients have a poor prognosis regardless of the BC subtype, especially in scenarios where newer therapeutic options are unavailable.
目的:中枢神经系统(CNS)转移是乳腺癌(BC)的一个重要负担。在这种情况下,卡培他滨是一种常见的选择,但支持其单药活性的数据却很少。我们旨在评估卡培他滨对乳腺癌中枢神经系统转移瘤的颅内疗效。方法:该回顾性队列包括在一个中心接受卡培他滨治疗的BC中枢神经系统转移患者。研究终点为颅内中枢神经系统客观反应率(CNS-ORR)、颅内中枢神经系统疾病控制率(CNS-DCR)、颅内中枢神经系统无进展生存期(CNS-PFS)和总生存期(OS)。结果:共纳入209例患者,其中41.6%为激素受体阳性HER2-阴性(HR + HER2-),33.9%为人表皮生长因子受体2阳性(HER2+),26.4%为三阴性乳腺癌(TNBC)。90.4%的患者接受了放疗,27.5%的患者接受了中枢神经系统手术。在可获得颅内反应的患者中,3个月CNS-ORR和CNS-DCR分别为41.6%和81.2%。TNBC患者的CNS-ORR更高(61%对HR + HER2-BC的38%和HER2 + BC的35%)(P = 0.194)。如果将 3 个月时无法评估的患者视为无应答者,则 3 个月的 CNS-ORR 为 19.1%(HR + HER2 为 18.4%,HER2+ 为 18.3%,TNBC 为 21.6%)。然而,TNBC与较低的CNS-PFS(P < 0.001)和OS(P < 0.001)相关。HR + HER2的中位生存期为8.3个月,HER2+为5.0个月,TNBC为3.0个月。中位OS分别为8.7个月、9.1个月和4.5个月。结论在3个月后可获得颅内反应的中枢神经系统转移的BC患者中,卡培他滨可观察到颅内活性。无论 BC 属于哪种亚型,这些患者的预后都很差,尤其是在没有新的治疗方案的情况下。
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引用次数: 0
Current scenario and future perspectives of clinical research in Brazil: a national survey 巴西临床研究的现状和未来展望:全国调查
Pub Date : 2023-11-23 DOI: 10.3332/ecancer.2023.1640
Heloisa Resende, T. Rebelatto, Gustavo Werutsky, Gustavo Gossling, Vinícius Aguiar, Guilherme M C Lopes, Biazi R de Assis, Lilian Arruda, Carlos H Barrios
Background: Epidemiological and clinical cancer research is essential to understanding tumour behaviour and developing
背景:癌症的流行病学和临床研究对于了解肿瘤的行为和制定治疗方案至关重要。
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引用次数: 0
Young Filipino breast cancer patients have worse survival outcomes 菲律宾年轻乳腺癌患者的生存率较低
Pub Date : 2023-11-23 DOI: 10.3332/ecancer.2023.1639
R. V. Yap, Deanne Lou Marquez, Frances Marion De La Serna
Background: In the 2020 GLOBOCAN report, breast cancer is the 3rd most common cause of cancer-related mortality in the Philippines. The incidence of breast cancer in the young (≤40 years) was reported to be higher in the Philippines compared to other Asian countries. Several studies have consistently demonstrated poor survival outcomes in this age group due to its aggressiveness and unique tumour biology. However, data on survival outcomes of young Filipino breast cancer patients remains unknown in the Philippines. Methods: A retrospective study was performed involving patients with stage I–III breast cancer who underwent definitive surgery from January 2010 to December 2015 at a single-tertiary institution. Patients were grouped according to age (≤40 and >40 years old). Their clinicopathological characteristics, treatment profile and 5-year survival outcomes were analyzed. Results: A total of 524 Filipino patients (15.1% aged ≤40 years) were included. Younger patients were diagnosed at a higher stage and pathologic grade. A negative hormone receptor, high Ki67 status, and triple negative breast cancer (TNBC) subtypes were also more common among younger patients. The overall breast-conserving surgery rate was low at 8.9%. The use of adjuvant chemoradiotherapy was more common and both 5-year overall survival (OS) and disease-free survival (DFS) were lower (61.1% versus 77.1% and 31.1% versus 66.8%, respectively) in the ≤40-year-old group. In the multivariate analysis, age group, tumour size, and nodal status were significant predictors for DFS. However, only tumour size was significant for OS. Conclusion: Young Filipino breast cancer patients have demonstrated unique pathologic characteristics with associated lower survival outcomes similar to the published literature. Increasing awareness of cancer screening practices among young women, provision of equitable access to healthcare, and prompt management of breast cancer in the young are crucial.
背景:在《2020 年全球乳腺癌报告》中,乳腺癌是菲律宾癌症相关死亡率的第三大常见病因。据报道,与其他亚洲国家相比,菲律宾年轻人(≤40 岁)的乳腺癌发病率较高。多项研究一致表明,由于其侵袭性和独特的肿瘤生物学特性,该年龄组患者的生存率较低。然而,菲律宾年轻乳腺癌患者的生存结果数据仍不为人知。研究方法我们进行了一项回顾性研究,研究对象是2010年1月至2015年12月期间在一家三级医疗机构接受明确手术治疗的I-III期乳腺癌患者。患者按年龄分组(≤40 岁和大于 40 岁)。对他们的临床病理特征、治疗情况和5年生存结果进行了分析。结果共纳入了524名菲律宾患者(15.1%年龄小于40岁)。年轻患者的诊断分期和病理分级较高。激素受体阴性、高Ki67状态和三阴性乳腺癌(TNBC)亚型在年轻患者中也更为常见。总体保乳手术率较低,仅为 8.9%。年龄≤40岁组的患者更常使用辅助化放疗,5年总生存期(OS)和无病生存期(DFS)均较低(分别为61.1%对77.1%和31.1%对66.8%)。在多变量分析中,年龄组、肿瘤大小和结节状态是预测无病生存期的重要因素。然而,只有肿瘤大小对OS有显著影响。结论菲律宾年轻乳腺癌患者表现出独特的病理特征,相关的生存率较低,这与已发表的文献相似。提高年轻女性的癌症筛查意识、提供公平的医疗服务以及及时治疗年轻乳腺癌至关重要。
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引用次数: 0
Real-world data on triple-negative breast cancer in Latin America and the Caribbean 拉丁美洲和加勒比地区三阴性乳腺癌的真实世界数据
Pub Date : 2023-11-21 DOI: 10.3332/ecancer.2023.1635
K. A. Tiscoski, J. Giacomazzi, Matheus Soares Rocha, Gustavo Gössling, Gustavo Werutsky
Breast cancer (BC) is the most prevalent cancer in women in Latin America and the Carib-bean. We compiled real-world data (RWD) on the epidemiology, diagnosis, treatment, and patient outcomes of triple-negative breast cancer (TNBC), addressing the main barriers to optimal care in Latin America. The prevalence of TNBC varies between 11% and 38.5% of all BC cases diagnosed in the region, and TNBC primarily affects young patients. Delays in BC diagnosis, with consequent advanced disease stages and barriers to access efficient therapies, particularly due to high costs, negatively impact patient outcomes. Cancer clinical trials are an opportunity to access standard and novel therapies for patients with this aggressive BC subtype and thus must be prioritised. Finally, generating RWD and cost-effectiveness studies in a region with limited resources is critical for decision-makers to define the incorporation of new technologies for the treatment of BC.
乳腺癌(BC)是拉丁美洲和加勒比海地区女性发病率最高的癌症。我们汇编了有关三阴性乳腺癌(TNBC)的流行病学、诊断、治疗和患者预后的真实世界数据(RWD),解决了拉丁美洲最佳治疗的主要障碍。在该地区确诊的所有乳腺癌病例中,TNBC 的发病率介于 11% 和 38.5% 之间,TNBC 主要影响年轻患者。BC 诊断的延误导致疾病进入晚期,以及获得高效疗法的障碍,特别是由于高昂的费用,对患者的治疗效果产生了负面影响。癌症临床试验为这种侵袭性 BC 亚型患者提供了获得标准和新型疗法的机会,因此必须优先考虑。最后,在资源有限的地区开展RWD和成本效益研究对于决策者确定将新技术用于治疗BC至关重要。
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引用次数: 0
LuciA-15 – a real-world prospective study of PARP inhibitors for the treatment of patients with HER-2 negative metastatic breast cancer with germline and/or somatic mutation of BRCA genes or homologous recombination repair related genes LuciA-15 - PARP 抑制剂治疗 HER-2 阴性、BRCA 基因或同源重组修复相关基因发生种系和/或体细胞突变的转移性乳腺癌患者的真实世界前瞻性研究
Pub Date : 2023-11-21 DOI: 10.3332/ecancer.2023.1634
F. Petracci, Cynthia Villarreal-Garza, Facundo Argañaraz, Gonzalo Gómez Abuin, José Peñaloza, Marcos Ariel Flores, Luciano Piazzoni, Cecilia Riggi, Lucía Fabiano, Lucía González, Belén Cieplinski, Sergio Rivero, Ernesto Korbenfeld, Pablo Mandó
Background: Poly(adenosine diphosphate-ribose) polymerase inhibitors (PARPi) improve progression free survival among patients with HER2 negative (HER2-ve) advanced breast cancer (ABC) and a BRCA1 or BRCA2 mutation compared to chemotherapy (CT). The objective of this prospective study was to evaluate the clinical benefit of PARPi treat-ment in terms of response, outcomes and survival by breast cancer type and treatment in a Latin-American
背景:聚腺苷二磷酸核糖聚合酶抑制剂(PARPi与化疗(CT)相比,聚腺苷二磷酸核糖聚合酶抑制剂(PARPi)可改善HER2阴性(HER2-ve)晚期乳腺癌(ABC)和BRCA1或BRCA2突变患者的无进展生存期。这项前瞻性研究的目的是评估 PARPi 治疗的临床益处,即根据拉丁美洲的乳腺癌类型和治疗方法,评估 PARPi 治疗在反应、疗效和生存率方面的临床益处。
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引用次数: 0
Palbociclib in advanced stage hormone receptor-positive breast cancer: real- world data from a Chilean multicentre registry 帕博西尼(Palbociclib)治疗激素受体阳性晚期乳腺癌:来自智利多中心登记处的真实数据
Pub Date : 2023-11-21 DOI: 10.3332/ecancer.2023.1636
Benjamín Walbaum, José Miguel Reyes, Pablo Rodriguez, S. Muniz, L. Medina, C. Ibañez, T. Merino, Mauricio P Pinto, M. Bravo, Francisco Acevedo, José Bennett, C. Sánchez
Background: The addition of cyclin-dependent kinases inhibitors (CDKi) to endocrine therapy (ET) as the first-or second line treatment improves progression-free and overall survival (OS) in hormone receptor-positive, HER2 negative (HR+/HER2-) advanced stage breast cancer (ABC). Our study compared survival rates and prognostic factors in Chilean patients that used palbociclib as first or subsequent (≥second) lines of treatment in a real-world setting. Methods: Our retrospective population-cohort study included HR+/HER2-ABC patients. We calculated 5-year OS and performed a multivariate analysis to determine prognostic factors. Results: A total of 106 patients were included. Median age was 49 years (19–86), 28.3% (30) had de novo stage IV disease; 63% received palbociclib with ET as first line, 54% of them with aromatase inhibitor over fulvestrant. Median OS for the entire cohort was 99 months and 5-year OS was 69%. Patients that received first line palbociclib had a 5-year OS of 89% versus 43% for ET monotherapy or ≥second line palbociclib ( p = 0.0062). Multivariate analysis showed that the year at diagnosis and CDKi timing (first line versus ≥second line) were significantly associated with OS. Conclusion: Our real-world data show that first-line CDKi + ET provides a statistically significant benefit in OS versus ≥second line in HR+/HER2-ABC patients.
背景:在内分泌治疗(ET)的一线或二线治疗中加入细胞周期蛋白依赖性激酶抑制剂(CDKi)可改善激素受体阳性、HER2阴性(HR+/HER2-)晚期乳腺癌(ABC)患者的无进展生存期和总生存期(OS)。我们的研究比较了在真实世界中使用帕博西尼(palbociclib)作为一线或后续(≥二线)治疗的智利患者的生存率和预后因素。研究方法我们的回顾性人群队列研究纳入了HR+/HER2-ABC患者。我们计算了5年OS,并进行了多变量分析以确定预后因素。研究结果共纳入 106 例患者。中位年龄为49岁(19-86岁),28.3%(30人)患有新发IV期疾病;63%的患者接受了帕博西尼联合ET作为一线治疗,其中54%的患者使用芳香化酶抑制剂而非氟维司群。整个组群的中位OS为99个月,5年OS为69%。接受帕博西尼一线治疗的患者的5年生存率为89%,而接受ET单药治疗或≥二线帕博西尼治疗的患者的5年生存率为43% ( p = 0.0062)。多变量分析显示,诊断年份和 CDKi 时间(一线与≥二线)与 OS 显著相关。结论我们的实际数据显示,在HR+/HER2-ABC患者中,一线CDKi+ET与≥二线CDKi+ET相比,在OS方面具有统计学意义上的显著优势。
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引用次数: 0
Real-world data in patients with BRCA mutated breast cancer treated with poly (ADP-ribose) polymerase inhibitors 使用多聚(ADP-核糖)聚合酶抑制剂治疗 BRCA 基因突变乳腺癌患者的实际数据
Pub Date : 2023-11-21 DOI: 10.3332/ecancer.2023.1633
Evelyn Lilian Beas-Lozano, H. Verduzco-Aguirre, Roberto Gonzalez-Salazar, Y. Chávarri-Guerra
Breast cancer is the most common type of cancer globally. Hereditary breast cancer accounts for 10% of new cases and 4%–5% of cases are associated to pathogenic variants in BRCA1 or BRCA2 genes. In recent years, poly-adenosine-diphosphate-ribose polymerase inhibitors (PARPi) olaparib and talazoparib have been approved for patients with BRCA -associated, HER2 -negative breast cancer. These drugs have shown positive results in the early and advanced setting with a favourable toxicity profile based on the OlympiAD, OlympiA and EMBRACA phase 3 trials. However, patients included in these randomised trials are highly selected, making toxicity and efficacy in patients encountered in routine clinical care a concern. Since the approval of olaparib and talazoparib for advanced human epidermal growth factor receptor 2-negative (HER2-negative) breast cancer, several phase IIIb–IV trials, expanded access cohorts, and retrospective cohorts have provided information on the efficacy and tolerability of these treatments in patient subgroups underrepresented in the registration trials, such as older adults, patients with poor performance status, and heavily pretreated patients. The aim of this review is to present a critical review of the information regarding the use of PARPi in real-world breast cancer patients.
乳腺癌是全球最常见的癌症类型。遗传性乳腺癌占新发病例的 10%,4%-5% 的病例与 BRCA1 或 BRCA2 基因的致病变异有关。近年来,多聚腺苷-二磷酸核糖聚合酶抑制剂(PARPi)奥拉帕利(olaparib)和他拉唑帕利(talazoparib)被批准用于治疗 BRCA 相关、HER2 阴性乳腺癌患者。根据OlympiAD、OlympiA和EMBRACA三期试验的结果,这些药物在早期和晚期治疗中取得了积极的疗效,毒性反应良好。然而,这些随机试验中的患者都是经过严格筛选的,因此常规临床治疗中患者的毒性和疗效令人担忧。自奥拉帕利和他拉唑帕利被批准用于治疗晚期人表皮生长因子受体2阴性(HER2阴性)乳腺癌以来,一些IIIb-IV期试验、扩大入组和回顾性入组提供了这些疗法在注册试验中代表性不足的患者亚群中的疗效和耐受性信息,如老年人、表现状态不佳的患者和重度预处理患者。本综述旨在对现实世界中乳腺癌患者使用 PARPi 的相关信息进行批判性回顾。
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