Systemic treatment of patients with advanced pancreatic cancer — is there still a place for gemcitabine in the first-line setting? Experience of Polish oncology centers

IF 0.3 Q4 ONCOLOGY Oncology in Clinical Practice Pub Date : 2023-10-25 DOI:10.5603/ocp.97305
Ireneusz Raczyński, Patryk Zając, Joanna Streb, Bogumiła Czartoryska-Arłukowicz, Aleksandra Chruściana-Bołtuć, Małgorzata Talerczyk, Katarzyna Wierzbicka, Agnieszka Siedlaczek, Weronika Radecka, Michał Jurczyk, Barbara Radecka
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Abstract

Introduction. Despite some progress in the treatment of patients with pancreatic cancer, it is still a malignancy with a poor prognosis, which results from its rapid local growth with a tendency to infiltrate surrounding tissues and metastasize, and late diagnosis at the advanced stage. The use of multi-drug regimens and modern targeted therapies did not completely eliminate the use of gemcitabine in monotherapy, which is a therapeutic option mainly in patients with poor performance status, ineligible for more advanced therapies. This study aimed to evaluate the results of treatment with single-agent gemcitabine in everyday clinical practice in Poland and to attempt to identify the predictors of obtaining long-term responses resulting from this treatment. Material and methods. A retrospective analysis of 167 patients with advanced pancreatic cancer treated with single-agent gemcitabine in five oncology centers in Poland in the years 2017–2022 was conducted. Gemcitabine was used as monotherapy at an initial dose of 1000 mg/m2 of body surface area (BSA) weekly, 7 times in an 8-week cycle, then 3 times in a 4-week cycle. Results. Median overall survival (OS) in the entire group of patients was 6.1 months (range — 0.2–32.3 months), and median progression-free survival (PFS) was 4.2 months (range — 0.2–31.3 months). A group of 60 patients was identified as “long responders” (LR), with a response of at least 6 months and a group of 107 as “short responders” (SR). Median PFS in the LR group was 9.15 months (range — 6.0–31.3 months) and in the SR group, it was 3.2 months (range — 0.2–5.8 months). Median OS was 11.6 months (range — 5.9–30.8) and 3.8 months (range — 0.2–32.3 months), respectively. In multivariate analysis, the likelihood of achieving at least a 6-month response (LR) was assessed using a logistic regression model. The model takes into account four variables: the neutrophil/lymphocyte (NLR) ratio, liver metastases, sex, and Hb level. Conclusions. The obtained results confirm that gemcitabine monotherapy is still useful in the first-line treatment of patients with advanced and metastatic pancreatic adenocarcinoma. An appropriate selection of patients for this treatment may improve the results while maintaining lower toxicity compared to combined treatment.
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晚期胰腺癌患者的全身治疗——吉西他滨在一线是否仍有一席之地?有波兰肿瘤中心的工作经验
介绍。尽管胰腺癌患者的治疗取得了一些进展,但它仍然是一种预后较差的恶性肿瘤,这是因为它局部生长迅速,容易浸润周围组织并转移,晚期诊断较晚。多药方案和现代靶向治疗的使用并没有完全消除吉西他滨在单药治疗中的使用,单药治疗主要是治疗状态不佳、不符合更先进治疗条件的患者。本研究旨在评估波兰日常临床实践中单药吉西他滨治疗的结果,并试图确定这种治疗获得长期疗效的预测因素。材料和方法。回顾性分析了2017-2022年波兰5个肿瘤中心接受单药吉西他滨治疗的167例晚期胰腺癌患者。吉西他滨作为单药治疗,初始剂量为每周1000mg /m2体表面积(BSA), 8周周期7次,4周周期3次。结果。全组患者的中位总生存期(OS)为6.1个月(范围- 0.2-32.3个月),中位无进展生存期(PFS)为4.2个月(范围- 0.2-31.3个月)。一组60名患者被确定为“长反应者”(LR),反应至少6个月,一组107名患者被确定为“短反应者”(SR)。LR组的中位PFS为9.15个月(范围- 6.0-31.3个月),SR组为3.2个月(范围- 0.2-5.8个月)。中位OS分别为11.6个月(范围- 5.9-30.8)和3.8个月(范围- 0.2-32.3)。在多变量分析中,使用逻辑回归模型评估实现至少6个月缓解(LR)的可能性。该模型考虑了四个变量:中性粒细胞/淋巴细胞(NLR)比率、肝转移、性别和Hb水平。结论。获得的结果证实,吉西他滨单药治疗在晚期和转移性胰腺腺癌患者的一线治疗中仍然有用。与联合治疗相比,适当选择患者进行这种治疗可以改善结果,同时保持较低的毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.90
自引率
20.00%
发文量
46
审稿时长
15 weeks
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