The impact of bevacizumab intraperitoneal perfusion combined with paclitaxel and platinum-based chemotherapy on serum stromal-derived factor-1α (SDF-1α) and chemokine ligand 5 (CXCL-5) levels in patients with ovarian cancer after tumor cell debulking surgery.

IF 1.8 4区 医学 Q3 ONCOLOGY Anti-Cancer Drugs Pub Date : 2025-03-01 Epub Date: 2025-01-06 DOI:10.1097/CAD.0000000000001663
Liangliang Wang, Shanshan Ma, Huiwen Su, Dandan Nie, Lihua Wang
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Abstract

The aim of this study is to investigate the impact of bevacizumab intraperitoneal perfusion combined with paclitaxel and platinum-based chemotherapy on serum stromal-derived factor-1α (SDF-1α) and chemokine ligand 5 (CXCL-5) levels in patients with ovarian cancer after tumor cell debulking surgery. This clinical study was conducted on a cohort of 89 ovarian cancer patients who underwent tumor debulking surgery at our hospital from February 2020 to February 2021. The patients were divided into two groups using a random number table: the control group ( n  = 44) received postoperative treatment with paclitaxel and platinum-based chemotherapy, while the research group ( n  = 45) received additional treatment with intraperitoneal perfusion of bevacizumab in addition to the control group's treatment regimen. The analysis included an assessment of the clinical efficacy of both groups, changes in tumor biomarker levels before and after treatment, serum levels of SDF-1α and CXCL-5, T-lymphocyte subset levels, treatment-related adverse reactions, and a 2-year prognosis and survival assessment. The research group showed better performance compared to the control group in terms of disease remission rate (80.00% vs. 59.09%) and treatment effectiveness rate (95.56% vs. 75.00%) ( P  < 0.05). Before treatment, the levels of tumor biomarkers between the two groups were compared ( P  > 0.05). After treatment, the levels of serum ferritin, carbohydrate antigen 125, carbohydrate antigen 199, and human epididymis protein 4 in both groups significantly decreased compared to before treatment, with the research group having lower levels ( P  < 0.05). Before treatment, serum levels of SDF-1α and CXCL-5 between the two groups were compared ( P  > 0.05). After treatment, however, the levels of SDF-1α and CXCL-5 significantly decreased compared to before treatment, with the research group having lower levels than the control group ( P  < 0.05). Before treatment, there was no difference in T-lymphocyte levels between the two groups ( P  > 0.05). In the control group, there was no significant change in T-lymphocyte levels before and after treatment ( P  > 0.05). In the research group, however, after treatment, each indicator increased compared to before treatment, and posttreatment levels of all indicators were higher than those in the control group ( P  < 0.05). The adverse reactions were compared between the two groups ( P  > 0.05). The research group had a longer average survival time than the control group, with 1-year and 2-year survival rates higher than the control group ( P  < 0.05). There was, however, no significant difference between the two groups in terms of local recurrence and metastasis ( P  > 0.05). In conclusion, bevacizumab intraperitoneal perfusion combined with paclitaxel and platinum-based chemotherapy shows better clinical efficacy in the treatment of ovarian cancer after tumor cell debulking surgery. It can significantly reduce the levels of serum SDF-1α and CXCL-5 in patients, improve survival rates, and demonstrate good safety.

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贝伐单抗腹腔灌注联合紫杉醇、铂类化疗对卵巢癌患者肿瘤细胞去膨胀手术后血清基质衍生因子-1α (SDF-1α)和趋化因子配体5 (CXCL-5)水平的影响
本研究旨在探讨贝伐单抗腹腔灌注联合紫杉醇和铂类化疗对卵巢癌患者肿瘤细胞去膨胀手术后血清基质衍生因子-1α (SDF-1α)和趋化因子配体5 (CXCL-5)水平的影响。本临床研究是对2020年2月至2021年2月在我院行肿瘤减体积手术的89例卵巢癌患者进行队列研究。采用随机数字表法将患者分为两组:对照组(n = 44)术后给予紫杉醇和铂类化疗,研究组(n = 45)在对照组治疗方案的基础上给予贝伐单抗腹腔灌注治疗。分析包括评估两组患者的临床疗效、治疗前后肿瘤生物标志物水平的变化、血清SDF-1α和CXCL-5水平、t淋巴细胞亚群水平、治疗相关不良反应以及2年预后和生存评估。研究组在疾病缓解率(80.00% vs. 59.09%)和治疗有效率(95.56% vs. 75.00%)方面均优于对照组(P < 0.05)。治疗后,两组患者血清铁蛋白、碳水化合物抗原125、碳水化合物抗原199、人附睾蛋白4水平均较治疗前显著降低,其中研究组较治疗前降低(P < 0.05)。治疗后,SDF-1α、CXCL-5水平较治疗前显著降低,且研究组低于对照组(P < 0.05)。对照组治疗前后t淋巴细胞水平差异无统计学意义(P < 0.05)。而研究组治疗后各项指标均较治疗前升高,且治疗后各项指标均高于对照组(P < 0.05)。研究组患者平均生存时间长于对照组,1年、2年生存率均高于对照组(P < 0.05)。综上所述,贝伐单抗腹腔灌注联合紫杉醇和铂类化疗治疗卵巢癌肿瘤细胞减体积手术后的临床疗效更好。可显著降低患者血清SDF-1α和CXCL-5水平,提高生存率,安全性好。
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来源期刊
Anti-Cancer Drugs
Anti-Cancer Drugs 医学-药学
CiteScore
3.80
自引率
0.00%
发文量
244
审稿时长
3 months
期刊介绍: Anti-Cancer Drugs reports both clinical and experimental results related to anti-cancer drugs, and welcomes contributions on anti-cancer drug design, drug delivery, pharmacology, hormonal and biological modalities and chemotherapy evaluation. An internationally refereed journal devoted to the fast publication of innovative investigations on therapeutic agents against cancer, Anti-Cancer Drugs aims to stimulate and report research on both toxic and non-toxic anti-cancer agents. Consequently, the scope on the journal will cover both conventional cytotoxic chemotherapy and hormonal or biological response modalities such as interleukins and immunotherapy. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors without further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool.
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The impact of bevacizumab intraperitoneal perfusion combined with paclitaxel and platinum-based chemotherapy on serum stromal-derived factor-1α (SDF-1α) and chemokine ligand 5 (CXCL-5) levels in patients with ovarian cancer after tumor cell debulking surgery. WISP1 inhibition of YAP phosphorylation drives breast cancer growth and chemoresistance via TEAD4 activation. A dual thermo/pH-sensitive hydrogel as 5-Fluorouracil carrier for breast cancer treatment. Albumin-based nanocarriers loaded with novel Zn(II)-thiosemicarbazone compounds chart a new path for precision breast cancer therapy. Comprehensive analysis of DNA methylation and gene expression to identify tumor suppressor genes reactivated by MLN4924 in acute myeloid leukemia.
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