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

KMBP en WGS – Middagsymposium en rondleiding Hartwig Medical Foundation – 22 maart 2024

KMBP en WGS – Middagsymposium en rondleiding Hartwig Medical Foundation – 22 maart 2024

21-12-2023

Nu Whole Genome Sequencing (WGS) steeds vaker wordt toegepast in de routinediagnostiek groeit ook de rol van de afdeling pathologie …

‘Om echt te weten hoe kanker ontstaat, heb je gegevens van echte patiënten nodig’

‘Om echt te weten hoe kanker ontstaat, heb je gegevens van echte patiënten nodig’

04-09-2017

Onderzoeker over datagebruik Ruben van Boxtel, senior post-doc bij het Center for Molecular Medicine van het UMC Utrecht maakt gebruik …

Voor onderzoek naar zeldzame kankers is samenwerking essentieel 

Voor onderzoek naar zeldzame kankers is samenwerking essentieel 

28-02-2025

28 februari is het internationale Rare Disease Day:  Zeldzame Ziekten Dag. We spraken met professor Stefan Fröhling over zijn onderzoek …

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