Molecular analysis in pancreatic adenocarcinoma: a real-world study from high-volume French centres (CAPANCOBIO study)

C. Evrard , M. Brugel , G. Piessen , G. Roth , N. Williet , V. Hautefeuille , H. Trelohan , M. Muller , O. Bouché , D. Tougeron
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Abstract

Background

In pancreatic adenocarcinoma (PA) it is crucial to better understand the molecular biology and identify targetable molecular alterations to obtain therapeutic improvements.

Methods

The aim of the CAPANCOBIO study was to assess routine clinical practice regarding tumour somatic molecular analysis (SMA) in patients with unresectable PA. Tumour SMAs for patients with advanced PA were collected in nine high-volume French centres from September 2019 to October 2021 to identify factors influencing the prescription of SMA.

Results

Among the 397 patients included in the CAPANCOBIO study, 70 had an SMA (17.6%). The most frequent tests were next-generation sequencing analysis (70.0%). Among the 70 patients with SMA, 31 (44.3%) had at least one alteration detected, but only 6 patients had targetable alterations. Among these, only one patient (n = 1/6, 16.6%) was included in a clinical trial. Patients with SMA were younger (P < 0.0001), more often female (P = 0.007), and more frequently had a family history of the BRCA cancer spectrum (P = 0.017).

Conclusions

Few patients with advanced PA had SMA of the tumour. Despite patients with targetable molecular alterations identified, very few patients were treated with targeted therapy and/or included in a clinical trial. It is essential to increase SMA for advanced PA in routine clinical practice to increase the use of targeted therapy and inclusions in clinical trials.
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胰腺腺癌的分子分析:来自法国高容量中心的真实世界研究(CAPANCOBIO研究)
在胰腺腺癌(PA)中,更好地了解分子生物学和识别可靶向的分子改变对于获得治疗改进至关重要。方法CAPANCOBIO研究的目的是评估不可切除PA患者肿瘤体细胞分子分析(SMA)的常规临床实践。2019年9月至2021年10月,在法国9个高容量中心收集了晚期PA患者的肿瘤SMA,以确定影响SMA处方的因素。结果在CAPANCOBIO研究中纳入的397例患者中,70例患有SMA(17.6%)。最常见的检测是新一代测序分析(70.0%)。在70例SMA患者中,31例(44.3%)至少检测到一种改变,但只有6例患者具有可靶向的改变。其中,仅有1例患者(n = 1/6, 16.6%)被纳入临床试验。SMA患者较年轻(P <;0.0001),女性多见(P = 0.007),有BRCA家族病史者多见(P = 0.017)。结论晚期前列腺癌患者很少出现肿瘤SMA。尽管确定了可靶向分子改变的患者,但很少有患者接受靶向治疗和/或纳入临床试验。在常规临床实践中增加晚期PA的SMA,以增加临床试验中靶向治疗和包涵体的使用是必不可少的。
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