DR-132 ctDNA analysis to monitor response to neoadjuvant chemoradiation in esohageal cancer patients

No Featured Image set

“After treatment with a combination of chemotherapy and radiotherapy for esophageal cancer, the current standard treatment is to continue with resection. However, in circa 20% of patients, no vital tumor cells are found in the resection specimen. On the other side, circa 10% of patients develop metastases shortly after esophageal resection. These patients could have possibly been spared esophagus resection. A nation-wide study, initiated by the department of surgery of the Erasmus MC, is currently recruiting patients (the SANO study, PI prof. dr. van Lanschot) and aims to clarify the role of esophagus resection in patients with no radiological or pathological (on biopsy) evidence of disease after pre-operative chemoradiation. A rapidly developing minimally invasive method to improve detection of minimal amounts of tumor cells or fragments could help to identity those patients in whom true cure has been accomplished. Therefor, we are currently biobanking blood of the patients in the SANO trial to serially measure tumor DNA in the blood

To come to a comprehensive panel of genetic variants to be measured in the blood, we wish to incorporate the genetic variants found in the metastases of esophageal cancer patients, as these variants are expected to be the drivers of resistance to treatment and disease recurrence. Also, we want to explore the genetic characteristics of metastases of esophageal cancer.

Discovering new genetic variants in metasatses that have not been identified in primary tumors could lead to new therapeutic approaches. Optimizing the blood assay could lead to a new and minimally inavsive means to monitor tumor response.”

Bianca Mostert Erasmus MC The Netherlands

Terug naar nieuws

Meer nieuws

Whole genome sequencing Hartwig ingezet in Finland

Whole genome sequencing Hartwig ingezet in Finland

10-07-2020

Sinds augustus 2019 gebruikt Docrates, een particulier instituut voor kankerbehandeling in Finland, de uitgebreide DNA-test van Hartwig Medical Foundation om …

In de media: Genomeweb: Gedeeltelijke vergoeding uitgebreide DNA-test in Nederland

In de media: Genomeweb: Gedeeltelijke vergoeding uitgebreide DNA-test in Nederland

09-04-2021

Deze week heeft ook de Amerikaanse website Precision Oncology News van Genomeweb aandacht besteed aan het nieuws dat de Tweede …

Karen Willemsen lid raad van toezicht Hartwig Medical Foundation 

Karen Willemsen lid raad van toezicht Hartwig Medical Foundation 

03-10-2024

Karen Willemsen is op 12 september benoemd tot lid van de raad van toezicht van Hartwig Medical Foundation (Hartwig).    Karen …

Wilt u op de hoogte blijven van nieuwe ontwikkelingen?

Abonneer u op onze nieuwsbrieven

Meer weten over de complete DNA-test?

Ga naar OncoAct.nl