Danny R. Youlden, Bryan A. Chan, Jon Clark, Victoria K. Donoghue, Michael J. Allen
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Multivariable Poisson models were fitted to determine factors associated with each type of chemotherapy, expressed as relative likelihoods (RLs). Variations in three-year observed survival were assessed using flexible parametric modelling and reported in terms of adjusted excess mortality hazard ratios (HRs).</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Of the 766 people in the study cohort, 59% were treated with GnP, 27% with mFFX, and 15% with GEM. After adjustment, treatment with mFFX was far more likely in selected private facilities compared to public hospitals (RL = 2.33, 95% CI 1.84–2.96), whereas the GEM regimen was used more often for those from outer regional/remote areas (RL = 2.20 compared to people living in major cities, 95% CI 1.45–3.34; <i>p</i> < 0.001). Three-year survival was very poor at just 5% (95% CI 3%–7%). 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引用次数: 0
摘要
不可切除胰腺癌患者的三种主要化疗方案包括改良的FOLFIRINOX(由奥沙利铂、伊立替康和氟尿嘧啶组成,标记为mFFX)、吉西他滨联合nab-紫杉醇(GnP)和单药吉西他滨(GEM)。我们探索了与化疗类型和生存率变化相关的特征。材料和方法从基于人群的昆士兰肿瘤数据库中提取2018年至2022年期间未切除的胰腺癌患者的记录,这些患者接受一线mFFX、GnP或GEM治疗。拟合多变量泊松模型来确定与每种化疗相关的因素,以相对可能性(RLs)表示。使用灵活的参数模型评估三年观察生存率的变化,并根据调整后的超额死亡率风险比(HRs)进行报告。在研究队列中的766名患者中,59%接受GnP治疗,27%接受mFFX治疗,15%接受GEM治疗。调整后,与公立医院相比,在选定的私立医院中使用mFFX治疗的可能性要大得多(RL = 2.33, 95% CI 1.84-2.96),而来自外部地区/偏远地区的患者更常使用GEM方案(RL = 2.20,与居住在主要城市的人相比,95% CI 1.45-3.34; p < 0.001)。三年生存率非常低,只有5% (95% CI 3%-7%)。尽管如此,与mFFX相比,GnP (HR = 1.30, 95% CI 1.07-1.59)和GEM (HR = 1.53, 95% CI 1.17-2.01)的调整死亡率更高。结论对于不能切除的胰腺癌,除临床指征外,治疗应公平。然而,我们的研究结果表明,一个人的生活地点和他们接受治疗的设施类型可能会影响他们的化疗方案。
Treatment and Survival for Unresectable Pancreatic Adenocarcinoma in Queensland, Australia, 2018–2022
Background
The three main chemotherapy regimens for people with unresectable pancreatic cancer include modified FOLFIRINOX (comprising oxaliplatin, irinotecan and fluorouracil, denoted mFFX), gemcitabine with nab-paclitaxel (GnP), and single-agent gemcitabine (GEM). We explored characteristics associated with the type of chemotherapy and variations in survival.
Materials and Methods
Records for people with unresected pancreatic adenocarcinoma between 2018 and 2022 treated with first-line mFFX, GnP or GEM were extracted from the population-based Queensland Oncology Repository. Multivariable Poisson models were fitted to determine factors associated with each type of chemotherapy, expressed as relative likelihoods (RLs). Variations in three-year observed survival were assessed using flexible parametric modelling and reported in terms of adjusted excess mortality hazard ratios (HRs).
Results
Of the 766 people in the study cohort, 59% were treated with GnP, 27% with mFFX, and 15% with GEM. After adjustment, treatment with mFFX was far more likely in selected private facilities compared to public hospitals (RL = 2.33, 95% CI 1.84–2.96), whereas the GEM regimen was used more often for those from outer regional/remote areas (RL = 2.20 compared to people living in major cities, 95% CI 1.45–3.34; p < 0.001). Three-year survival was very poor at just 5% (95% CI 3%–7%). Nonetheless, adjusted mortality was higher for GnP (HR = 1.30, 95% CI 1.07–1.59) and GEM (HR = 1.53, 95% CI 1.17–2.01) compared to mFFX.
Conclusions
Apart from clinical indications, there should be equity in the treatment received for unresectable pancreatic cancer. Our results suggest, however, that where a person lives and the type of facility at which they are treated may influence their chemotherapy regimen.
期刊介绍:
Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas:
Clinical Cancer Research
Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations
Cancer Biology:
Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery.
Cancer Prevention:
Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach.
Bioinformatics:
Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers.
Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.