转移性透明细胞肉瘤序贯化疗的实际效果。

IF 1.9 4区 医学 Q3 INFECTIOUS DISEASES Journal of Chemotherapy Pub Date : 2024-07-08 DOI:10.1080/1120009X.2024.2372524
Anna M Czarnecka, Paulina Chmiel, Piotr J Błoński, Tomasz Świtaj, Paweł Rogala, Sławomir Falkowski, Hanna Koseła-Paterczyk, Paweł Teterycz, Tadeusz Morysiński, Mateusz Spałek, Michał Wągrodzki, Piotr Rutkowski
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引用次数: 0

摘要

透明细胞肉瘤是软组织肉瘤中极为罕见的化疗耐药亚型。这项回顾性分析旨在通过评估一家转诊中心的反应率、无进展生存期(PFS)和总生存期(OS),明确姑息化疗对透明细胞肉瘤的疗效。该研究对1997年至2023年期间在肉瘤科接受姑息治疗的CCS患者进行了回顾性分析。采用RECIST标准评估治疗反应,并采用卡普兰-梅耶法计算PFS和OS。分析涵盖了23名接受过CCS化疗的患者,其中男性11人(占47.8%)。开始接受姑息治疗时的中位年龄为32岁(18-59岁不等)。中位随访时间为 8.2 个月。4名患者因M1疾病转诊至本中心,6名患者接受了围手术期化疗,并在随访期间病情恶化。在一线化疗中,14名患者接受了蒽环类化疗(60.9%),5名患者接受了伊福酰胺(HD-IFO)治疗,4名患者接受了其他治疗方案。1名患者(4.3%)获得部分反应(PR),12名患者(52.2%)获得最佳反应--疾病稳定(SD)。一线治疗的中位生存期为2.79个月(95% CI:2.04-8.38),二线治疗的中位生存期为1.76个月(95% CI:0.72-6.97)。一线姑息化疗的中位OS为8.2个月(95% CI:6.2-14),二线姑息化疗的中位OS为4.6个月(95% CI:3.9-NA)。围手术期蒽环类药物治疗使M1患者的中位PFS恶化。CCS患者对常规化疗的反应不佳,这表明有必要在这一适应症中开展进一步的临床试验。
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Real-world outcomes of metastatic clear cell sarcoma sequential chemotherapy.

Clear cell sarcoma is an ultra-rare chemoresistant subtype of soft tissue sarcoma. This retrospective analysis aimed to clarify the efficacy of palliative chemotherapy in CCS by assessing response rates, progression-free survival (PFS), and overall survival (OS) at a referral center. A retrospective analysis of palliative treatment was conducted on patients with CCS treated at the sarcoma unit from 1997 to 2023. Treatment responses were assessed using RECIST criteria, and the Kaplan-Meier method was used to calculate PFS and OS. The analysis covered 23 CCS chemotherapy-treated patients with 11 (47.8%) men. The median age at the palliative treatment start was 32 years (range 18-59). The median follow-up was 8.2 months. Four patients were referred to our centre for M1 disease, and 6 received perioperative chemotherapy and progressed during follow-up. In the first line, 14 patients received anthracycline-based chemotherapy (60.9%), five were treated with ifosfamide (HD-IFO), and four received other regimens. One patient (4.3%) achieved partial response (PR), and 12 patients (52.2%) achieved stable disease (SD) as the best response. Median PFS in 1 line was 2.79 months (95% CI: 2.04-8.38), and 1.76 months (95% CI: 0.72-6.97) in the second line. The median OS from first-line palliative chemotherapy was 8.2 months (95% CI: 6.2-14), and the second-line palliative chemotherapy mOS was 4.6 months (95% CI: 3.9-NA). Perioperatively anthracycline-pretreated worsened patients' median PFS in the M1 setting. Poor responses to conventional chemotherapy were observed in CCS, indicating a need for further clinical trials in this indication.

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来源期刊
Journal of Chemotherapy
Journal of Chemotherapy 医学-药学
CiteScore
3.70
自引率
0.00%
发文量
144
审稿时长
6-12 weeks
期刊介绍: The Journal of Chemotherapy is an international multidisciplinary journal committed to the rapid publication of high quality, peer-reviewed, original research on all aspects of antimicrobial and antitumor chemotherapy. The Journal publishes original experimental and clinical research articles, state-of-the-art reviews, brief communications and letters on all aspects of chemotherapy, providing coverage of the pathogenesis, diagnosis, treatment, and control of infection, as well as the use of anticancer and immunomodulating drugs. Specific areas of focus include, but are not limited to: · Antibacterial, antiviral, antifungal, antiparasitic, and antiprotozoal agents; · Anticancer classical and targeted chemotherapeutic agents, biological agents, hormonal drugs, immunomodulatory drugs, cell therapy and gene therapy; · Pharmacokinetic and pharmacodynamic properties of antimicrobial and anticancer agents; · The efficacy, safety and toxicology profiles of antimicrobial and anticancer drugs; · Drug interactions in single or combined applications; · Drug resistance to antimicrobial and anticancer drugs; · Research and development of novel antimicrobial and anticancer drugs, including preclinical, translational and clinical research; · Biomarkers of sensitivity and/or resistance for antimicrobial and anticancer drugs; · Pharmacogenetics and pharmacogenomics; · Precision medicine in infectious disease therapy and in cancer therapy; · Pharmacoeconomics of antimicrobial and anticancer therapies and the implications to patients, health services, and the pharmaceutical industry.
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