Neoadjuvant chemotherapy is associated with a transient increase of intratumoral T-cell density in microsatellite stable colorectal liver metastases. Issue 5 (3rd May 2020)

• Record Type: Journal Article
• Authors: Dagenborg, Vegar Johansen; Marshall, Serena Elizabeth; Yaqub, Sheraz; Grzyb, Krzysztof; Boye, Kjetil; Lund-Iversen, Marius; Høye, Eirik; Berstad, Audun E; Fretland, Åsmund Avdem; Edwin, Bjørn; Ree, Anne Hansen; Flatmark, Kjersti
• Is Part Of: Cancer biology & therapy. Volume 21:Issue 5(2020)
• Page Start: 432
• Page End: 440
• Publication Date: 2020-05-03
• Subjects: Liver metastases -- colorectal cancer -- neoadjuvant chemotherapy -- immunogenic cell death -- t-cell densities -- immune check-point inhibition; 616.99406
• DOI: 10.1080/15384047.2020.1721252
• Languages: English
• ISSNs: 1538-4047

Abstract

ABSTRACT: Patients with colorectal liver metastases (CLM) commonly receive neoadjuvant chemotherapy (NACT) prior to surgical resection. NACT may induce immunogenic cell death with subsequent recruitment of T-cells to the tumor microenvironment, which could be exploited by immune checkpoint inhibition (ICI). In theory, this could expand the use of ICI to obtain responses also in microsatellite stable colorectal cancer, but evidence to suggest optimal treatment schedules are lacking. In this study, densities of total-, cytotoxic-, helper- and regulatory T-cells were quantified by immunohistochemistry in resected CLM from 92 patients included in the OSLO-COMET trial (NCT01516710). All but one patient had microsatellite stable tumors (91/92). Associations between T-cell densities and clinicopathological parameters were analyzed. Fluoropyrimidine-based NACT (in most cases with addition of oxaliplatin or irinotecan) was administered to 45 patients completed median 8 weeks prior to surgical resection. No overall association was found between NACT administration and intratumoral T-cell densities. However, within the NACT group, a short time interval (<9.5 weeks) between NACT completion and CLM resection was strongly associated with high intratumoral T-cell densities compared to the long-interval and no NACT groups (medians 491, 236, and 292 cells/mm 2, respectively; P < .0001). The results from this study suggest that the observed increase in intratumoral T-cells after NACT administration may be transient. The significance of this finding should be further explored to ensure that optimal treatment schedules are chosen for studies combining cytotoxic chemotherapy and ICI.