Nóra Ecker, Marietta Aranyi, Edina Kiss, Nóra Kiss, Erika Lahm, Zsófia Nagy, Márta Sikter, Ádám Szabó, Anikó Szászné Szentesi, Klára Takács, Andrea Uhlyarik, József Vachaja, Barbara Sebők, Zsuzsanna Pápai
{"title":"帕唑帕尼治疗局部晚期和转移性软组织肉瘤的现实经验:匈牙利回顾性单中心研究。","authors":"Nóra Ecker, Marietta Aranyi, Edina Kiss, Nóra Kiss, Erika Lahm, Zsófia Nagy, Márta Sikter, Ádám Szabó, Anikó Szászné Szentesi, Klára Takács, Andrea Uhlyarik, József Vachaja, Barbara Sebők, Zsuzsanna Pápai","doi":"10.3389/pore.2025.1611965","DOIUrl":null,"url":null,"abstract":"<p><p>Pazopanib is a tyrosine-kinase inhibitor also used for the treatment of advanced soft tissue sarcomas. Our retrospective study analyzed real-world data of stage 4 sarcoma patients treated with pazopanib in our department in the past 10 years. Data were collected from the Medworks medical system, which is used for daily work in our center. A total of 99 patients were included: 46 men and 53 women The median age at the diagnosis was 49.8 years. The most common histological subtypes were leiomyosarcoma and synovial sarcoma. All patients received 800 mg of pazopanib per day, which was reduced to 400 mg in the event of toxicity. Treatment was continued until disease progression or unmanageable toxicity. The primary endpoint of the study was progression-free survival and the secondary endpoints were overall survival, overall response rate and disease control rate. The results in relation to demographic data, previous treatments, localizations of primary tumors and metastasis and histological subtypes were analyzed. In our center pazopanib was most frequently used in the third line. In total, 61 patients received perioperative therapy; the most common regimen used in the metastatic setting was VIP. Median PFS and OS were 3 months and 7 months, respectively. ORR was 14% and DCR was 40.45%. Dose reductions were necessary during the treatment of 56 patients. Hematological toxicity was detected in 23% of cases, with the most frequent events being grade 1 thrombocytopenia and grade 2 leukocytopenia. Non-hematological adverse events were documented in half of the patients. Pazopanib was more effective in earlier lines of treatment. Compared to the PALETTE phase 3 trial more patients received perioperative therapy, median PFS and OS were shorter (3 months vs. 4.6 months and 7 months vs. 11.9 months) and ORR was higher (14% vs. 9%) in our patient population. Dose reductions were more frequent in our center. Pazopanib is a therapeutic option for the treatment of advanced soft tissue sarcoma, also according to real-world data. 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引用次数: 0
摘要
Pazopanib是一种酪氨酸激酶抑制剂,也用于治疗晚期软组织肉瘤。我们的回顾性研究分析了过去10年来我科接受帕唑帕尼治疗的4期肉瘤患者的真实数据。数据来自Medworks医疗系统,该系统用于我中心的日常工作。共纳入99例患者:男性46例,女性53例,诊断时中位年龄49.8岁。最常见的组织学亚型为平滑肌肉瘤和滑膜肉瘤。所有患者每天接受800毫克帕唑帕尼,在发生毒性事件时减少到400毫克。治疗一直持续到疾病进展或出现无法控制的毒性。研究的主要终点是无进展生存期,次要终点是总生存期、总缓解率和疾病控制率。结果与人口统计学数据、既往治疗、原发肿瘤和转移的定位以及组织学亚型有关。在我们的中心,帕唑帕尼最常用于三线治疗。61例患者接受围手术期治疗;在转移性肿瘤中最常用的治疗方案是VIP。中位PFS和OS分别为3个月和7个月。ORR为14%,DCR为40.45%。56例患者在治疗过程中需要减少剂量。23%的病例检测到血液毒性,最常见的事件是1级血小板减少症和2级白细胞减少症。半数患者记录了非血液学不良事件。帕唑帕尼在早期治疗中更有效。与PALETTE 3期试验相比,更多患者接受围手术期治疗,中位PFS和OS更短(3个月vs 4.6个月,7个月vs 11.9个月),ORR更高(14% vs 9%)。剂量减少在我们中心更为频繁。根据现实世界的数据,Pazopanib是治疗晚期软组织肉瘤的治疗选择。需要进一步的研究来选择从帕唑帕尼获益最多的患者,并确定最合适的治疗顺序。
Real-world experience with pazopanib in locally advanced and metastatic soft tissue sarcomas: a Hungarian retrospective single-center study.
Pazopanib is a tyrosine-kinase inhibitor also used for the treatment of advanced soft tissue sarcomas. Our retrospective study analyzed real-world data of stage 4 sarcoma patients treated with pazopanib in our department in the past 10 years. Data were collected from the Medworks medical system, which is used for daily work in our center. A total of 99 patients were included: 46 men and 53 women The median age at the diagnosis was 49.8 years. The most common histological subtypes were leiomyosarcoma and synovial sarcoma. All patients received 800 mg of pazopanib per day, which was reduced to 400 mg in the event of toxicity. Treatment was continued until disease progression or unmanageable toxicity. The primary endpoint of the study was progression-free survival and the secondary endpoints were overall survival, overall response rate and disease control rate. The results in relation to demographic data, previous treatments, localizations of primary tumors and metastasis and histological subtypes were analyzed. In our center pazopanib was most frequently used in the third line. In total, 61 patients received perioperative therapy; the most common regimen used in the metastatic setting was VIP. Median PFS and OS were 3 months and 7 months, respectively. ORR was 14% and DCR was 40.45%. Dose reductions were necessary during the treatment of 56 patients. Hematological toxicity was detected in 23% of cases, with the most frequent events being grade 1 thrombocytopenia and grade 2 leukocytopenia. Non-hematological adverse events were documented in half of the patients. Pazopanib was more effective in earlier lines of treatment. Compared to the PALETTE phase 3 trial more patients received perioperative therapy, median PFS and OS were shorter (3 months vs. 4.6 months and 7 months vs. 11.9 months) and ORR was higher (14% vs. 9%) in our patient population. Dose reductions were more frequent in our center. Pazopanib is a therapeutic option for the treatment of advanced soft tissue sarcoma, also according to real-world data. Further investigations are needed to select patients who can benefit the most from pazopanib and to determine the most appropriate sequence of therapy.
期刊介绍:
Pathology & Oncology Research (POR) is an interdisciplinary Journal at the interface of pathology and oncology including the preclinical and translational research, diagnostics and therapy. Furthermore, POR is an international forum for the rapid communication of reviews, original research, critical and topical reports with excellence and novelty. Published quarterly, POR is dedicated to keeping scientists informed of developments on the selected biomedical fields bridging the gap between basic research and clinical medicine. It is a special aim for POR to promote pathological and oncological publishing activity of colleagues in the Central and East European region. The journal will be of interest to pathologists, and a broad range of experimental and clinical oncologists, and related experts. POR is supported by an acknowledged international advisory board and the Arányi Fundation for modern pathology.