The real-world efficacy and toxicity of first-line paclitaxel and cisplatin with bevacizumab in platinum-naïve primary stage IVB cervical cancer

IF 2 4区 医学 Q2 OBSTETRICS & GYNECOLOGY
Junhwan Kim , Eun-Byul Park , Shin-Wha Lee , Jeong-Yeol Park , Dae-Yeon Kim , Dae-Shik Suh , Jong-Hyeok Kim , Yong-Man Kim , Ju-Hyun Kim
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Abstract

Objective

To investigate the real-world efficacy and toxicity of paclitaxel-cisplatin-bevacizumab and identify prognostic factors for paclitaxel-cisplatin-bevacizumab in platinum-naïve primary stage IVB cervical cancer.

Materials and methods

We retrospectively reviewed patients with stage IVB cervical cancer who received paclitaxel-cisplatin-bevacizumab as first-line treatment between July 2015 and December 2021 at Asan Medical Center, Korea. Patient data including clinicopathologic characteristics, imaging, paclitaxel-cisplatin-bevacizumab administration, recurrence, and survival were collected.

Results

Overall, 61 patients were included in this study. The median age of the patients was 56 (range, 28−79) years. Patients received a median of 9 (range, 2−30) cycles of paclitaxel-cisplatin-bevacizumab. The most common adverse event (all grades) during treatment was azotemia (80.3 %). Dose reduction and drug interruption were conducted in 41.0 % and 26.2 % of patients, respectively. The median progression-free survival (PFS) and the median overall survival (OS) were 11.8 (95 % confidence interval [CI], 9.3−14.2) and 24.3 (95 % CI, 16.9−31.7) months, respectively. Multivariate analysis indicated that cervical mass size reduction rate ≥40 % at the longest diameter was an independent prognostic factor for PFS (adjusted hazard ratio, 0.24; 95 % CI, 0.11−0.53; p < 0.001). The median PFS of the patients with cervical mass size reduction rate ≥40 % and <40 % were 13.7 (95 % CI, 10.9−16.5) and 5.9 (95 % CI, 0−12.6) months, respectively (p < 0.001).

Conclusion

Paclitaxel-cisplatin-bevacizumab is effective and tolerable as a first-line treatment for platinum-naïve primary stage IVB cervical cancer. Cervical mass size reduction rate ≥40 % during paclitaxel-cisplatin-bevacizumab treatment might be a potential prognostic factor for PFS in patients with platinum-naïve primary stage IVB cervical cancer.
紫杉醇顺铂联合贝伐单抗一线治疗platinum-naïve原发性IVB期宫颈癌的实际疗效和毒性
目的:探讨紫杉醇-顺铂-贝伐单抗治疗platinum-naïve原发性IVB期宫颈癌的实际疗效和毒性,并探讨紫杉醇-顺铂-贝伐单抗治疗的预后因素。材料和方法:我们回顾性分析了2015年7月至2021年12月在韩国牙山医疗中心接受紫杉醇-顺铂-贝伐单抗作为一线治疗的IVB期宫颈癌患者。收集患者资料,包括临床病理特征、影像学、紫杉醇-顺铂-贝伐单抗给药、复发和生存。结果:本研究共纳入61例患者。患者的中位年龄为56岁(28-79岁)。患者接受紫杉醇-顺铂-贝伐单抗治疗的中位周期为9(范围2-30)个周期。治疗期间最常见的不良事件(所有级别)是氮血症(80.3%)。减量和停药分别占41.0%和26.2%。中位无进展生存期(PFS)和中位总生存期(OS)分别为11.8个月(95%可信区间[CI], 9.3-14.2)和24.3个月(95% CI, 16.9-31.7)。多因素分析显示,最长直径处宫颈肿块缩小率≥40%是PFS的独立预后因素(校正风险比,0.24;95% ci, 0.11-0.53;结论:紫杉醇-顺铂-贝伐单抗作为治疗platinum-naïve原发性IVB期宫颈癌的一线药物是有效且耐受的。紫杉醇-顺铂-贝伐单抗治疗期间宫颈肿块缩小率≥40%可能是platinum-naïve原发性IVB期宫颈癌患者PFS的潜在预后因素。
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来源期刊
CiteScore
3.60
自引率
23.80%
发文量
207
审稿时长
4-8 weeks
期刊介绍: Taiwanese Journal of Obstetrics and Gynecology is a peer-reviewed journal and open access publishing editorials, reviews, original articles, short communications, case reports, research letters, correspondence and letters to the editor in the field of obstetrics and gynecology. The aims of the journal are to: 1.Publish cutting-edge, innovative and topical research that addresses screening, diagnosis, management and care in women''s health 2.Deliver evidence-based information 3.Promote the sharing of clinical experience 4.Address women-related health promotion The journal provides comprehensive coverage of topics in obstetrics & gynecology and women''s health including maternal-fetal medicine, reproductive endocrinology/infertility, and gynecologic oncology. Taiwan Association of Obstetrics and Gynecology.
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