Delayed tumor-draining lymph node irradiation preserves the efficacy of combined radiotherapy and immune checkpoint blockade in models of metastatic disease.
Irma TelarovicCarmen S M YongLisa KurzIrene VetrugnoSabrina ReichlAlba Sanchez FernandezHung-Wei ChengRona WinklerMatthias GuckenbergerAnja KiparBurkhard LudewigMartin PruschyPublished in: Nature communications (2024)
Cancer resistance to immune checkpoint inhibitors motivated investigations into leveraging the immunostimulatory properties of radiotherapy to overcome immune evasion and to improve treatment response. However, clinical benefits of radiotherapy-immunotherapy combinations have been modest. Routine concomitant tumor-draining lymph node irradiation (DLN IR) might be the culprit. As crucial sites for generating anti-tumor immunity, DLNs are indispensable for the in situ vaccination effect of radiotherapy. Simultaneously, DLN sparing is often not feasible due to metastatic spread. Using murine models of metastatic disease in female mice, here we demonstrate that delayed (adjuvant), but not neoadjuvant, DLN IR overcomes the detrimental effect of concomitant DLN IR on the efficacy of radio-immunotherapy. Moreover, we identify IR-induced disruption of the CCR7-CCL19/CCL21 homing axis as a key mechanism for the detrimental effect of DLN IR. Our study proposes delayed DLN IR as a strategy to maximize the efficacy of radio-immunotherapy across different tumor types and disease stages.
Keyphrases
- lymph node
- early stage
- locally advanced
- squamous cell carcinoma
- radiation induced
- neoadjuvant chemotherapy
- small cell lung cancer
- radiation therapy
- rectal cancer
- sentinel lymph node
- liver injury
- drug induced
- type diabetes
- dendritic cells
- immune response
- liver fibrosis
- regulatory t cells
- oxidative stress
- endothelial cells
- adipose tissue
- lymph node metastasis
- high glucose
- insulin resistance
- high fat diet induced