A Pilot, Prospective, Observational Study to Investigate the Value of NGS in Liquid Biopsies to Predict Tumor Response After Neoadjuvant Chemo-Radiotherapy in Patients With Locally Advanced Rectal Cancer: The LiBReCa Study

• Published in: Frontiers in oncology Vol. 12; p. 900945
• Main Authors: Roesel, Raffaello, Epistolio, Samantha, Molinari, Francesca, Saletti, Piercarlo, De Dosso, Sara, Valli, Mariacarla, Franzetti-Pellanda, Alessandra, Deantonio, Letizia, Biggiogero, Maira, Spina, Paolo, Popeskou, Sotirios Georgios, Cristaudi, Alessandra, Mongelli, Francesco, Mazzucchelli, Luca, Stefanini, Federico Mattia, Frattini, Milo, Christoforidis, Dimitri
• Format: Journal Article
• Language: English
• Published: Frontiers Media S.A 28.06.2022
• Subjects: circulating tumor DNA (ctDNA); LARC; liquid biopsy; next-generation sequencing; Oncology; rectal cancer (RC); watch and wait approach
• ISSN: 2234-943X; 2234-943X
• DOI: 10.3389/fonc.2022.900945

Introduction Circulating tumor DNA (ctDNA) correlates with the response to therapy in different types of cancer. However, in patients with locally advanced rectal cancer (LARC), little is known about how ctDNA levels change with neoadjuvant chemoradiation (Na-ChRT) and how they correlate with treatment response. This work aimed to explore the value of serial liquid biopsies in monitoring response after Na-ChRT with the hypothesis that this could become a reliable biomarker to identify patients with a complete response, candidates for non-operative management. Materials and Methods Twenty-five consecutive LARC patients undergoing long-term Na-ChRT therapy were included. Applying next-generation sequencing (NGS), we characterized DNA extracted from formalin-fixed paraffin embedded diagnostic biopsy and resection tissue and plasma ctDNA collected at the following time points: the first and last days of radiotherapy (T 0 , T end ), at 4 (T 4 ), 7 (T 7 ) weeks after radiotherapy, on the day of surgery (T op ), and 3–7 days after surgery (T post-op ). On the day of surgery, a mesenteric vein sample was also collected (T IMV ). The relationship between the ctDNA at those time-points and the tumor regression grade (TRG) of the surgical specimen was statistically explored. Results We found no association between the disappearance of ctDNA mutations in plasma samples and pathological complete response (TRG1) as ctDNA was undetectable in the majority of patients from Tend on. However, we observed that the poor (TRG 4) response to Na-ChRT was significantly associated with a positive liquid biopsy at the T op . Conclusions ctDNA evaluation by NGS technology may identify LARC patients with poor response to Na-ChRT. In contrast, this technique does not seem useful for identifying patients prone to developing a complete response.