Veyssière Hugo, Lusho Sejdi, Molnar Ioana, Kossai Myriam, Bernadach Maureen, Abrial Catherine, Bidet Yannick, Radosevic-Robin Nina, Durando Xavier
Université Clermont Auvergne, INSERM UMR 1240 « Imagerie Moléculaire et Stratégies Théranostiques », Centre Jean PERRIN, Clermont-Ferrand, France.
Division de Recherche Clinique, Délégation Recherche Clinique & Innovation, Centre Jean PERRIN, Clermont-Ferrand, France.
Front Oncol. 2021 Jun 25;11:653370. doi: 10.3389/fonc.2021.653370. eCollection 2021.
Triple negative breast cancer (TNBC) accounts for 10-20% of breast cancers but has no specific therapy. While TNBC may be more sensitive to chemotherapy than other types of breast cancer, it has a poor prognosis. Most TNBC relapses occur during the five years following treatment, however predictive biomarkers of metastatic relapse are still lacking. High tumour-infiltrating lymphocytes (TILs) levels before and after neo-adjuvant chemotherapy (NAC) are associated with lower relapse risk and longer survival but TILs assessment is highly error-prone and still not introduced into the clinic. Therefore, having reliable biomarker of relapse, but easier to assess, remains essential for TNBC management. Searching for such biomarkers among serum/plasma proteins, circulating tumoral DNA (ctDNA) and blood cells appear relevant.
This single-centre and prospective study aims to discover predictive biomarkers of TNBC relapse and particularly focuses on plasma proteins. Blood samples will be taken at diagnosis, on the day of first-line or post-NAC surgery, on the day of radiotherapy start, then 6 months and one year after radiotherapy. A blood sample will be taken at the time of metastatic relapse diagnosis. Blood samples will be used for circulating protein quantification, blood cell counts and circulating tumour DNA quantification. A tumour RNA signature, based on the analysis of the RNA expression of 6 genes, will also be tested from the initial biopsy taken routinely. In NAC patients, TILs quantity will be assessed on TNBC pre-treatment biopsy and surgical specimen.
INSTIGO belongs to category 2 interventional research on humans. This study has been approved by the SUDEST IV ethics committee and is conducted in accordance with the Declaration of Helsinki and General Data Protection Regulation (GDPR). Study findings will be published in peer-reviewed medical journals.
ClinicalTrials.gov, identifier NCT04438681.
三阴性乳腺癌(TNBC)占乳腺癌的10%-20%,但尚无特异性治疗方法。虽然TNBC可能比其他类型的乳腺癌对化疗更敏感,但其预后较差。大多数TNBC复发发生在治疗后的五年内,然而转移性复发的预测生物标志物仍然缺乏。新辅助化疗(NAC)前后高肿瘤浸润淋巴细胞(TILs)水平与较低的复发风险和较长的生存期相关,但TILs评估极易出错且仍未引入临床。因此,拥有可靠的复发生物标志物且易于评估,对于TNBC的管理仍然至关重要。在血清/血浆蛋白、循环肿瘤DNA(ctDNA)和血细胞中寻找此类生物标志物似乎是有意义的。
这项单中心前瞻性研究旨在发现TNBC复发的预测生物标志物,尤其侧重于血浆蛋白。将在诊断时、一线或NAC术后第一天、放疗开始当天、放疗后6个月和1年采集血样。在转移性复发诊断时采集血样。血样将用于循环蛋白定量、血细胞计数和循环肿瘤DNA定量。还将从常规采集的初始活检组织中检测基于6个基因RNA表达分析的肿瘤RNA特征。对于接受NAC的患者,将在TNBC治疗前活检组织和手术标本上评估TILs数量。
INSTIGO属于人类二类干预性研究。本研究已获得南欧四号伦理委员会批准,并按照《赫尔辛基宣言》和《通用数据保护条例》(GDPR)进行。研究结果将发表在同行评审的医学期刊上。
ClinicalTrials.gov,标识符NCT04438681。