Optimizing Dose and Timing in Magnetic Tracer Techniques for Sentinel Lymph Node Detection in Early Breast Cancers: The Prospective Multicenter SentiDose Trial.
Abdi-Fatah HersiLida PistiolisCarlos Dussan LuberthEva Vikhe-PatilFredrik NilssonImad MohammedRoger Olofsson BaggeFredrik WärnbergStaffan ErikssonAndreas KarakatsanisPublished in: Cancers (2021)
Superparamagnetic iron oxide nanoparticles (SPIO) are non-inferior to radioisotope and blue dye (RI + BD) for sentinel lymph node (SLN) detection. Previously, 2 mL SPIO (Sienna+®) in 3 mL NaCl was used. In this dose-optimizing study, lower doses of a new refined SPIO solution (Magtrace®) (1.5 vs. 1.0 mL) were tested in different timeframes (0-24 h perioperative vs. 1-7 days preoperative) and injections sites (subareolar vs. peritumoral). Two consecutive breast cancer cohorts (n = 328) scheduled for SLN-biopsy were included from 2017 to 2019. All patients received isotope ± blue dye as back-up. SLNs were identified primarily with the SentiMag® probe and thereafter a gamma-probe. The primary endpoint was SLN detection rate with SPIO. Analyses were performed as a one-step individual patient-level meta-analysis using patient-level data from the previously published Nordic Trial (n = 206) as a third, reference cohort. In 534 patients, the SPIO SLN detection rates were similar (97.5% vs. 100% vs. 97.6%, p = 0.11) and non-inferior to the dual technique. Significantly more SLNs were retrieved in the preoperative 1.0 mL cohort compared with 1.5 and the 2.0 mL cohorts (2.18 vs. 1.85 vs. 1.83, p = 0.003). Lower SPIO volumes injected up to 7 days before the operation have comparable efficacy to standard SPIO dose and RI + BD for SLN detection.
Keyphrases
- sentinel lymph node
- early stage
- lymph node
- end stage renal disease
- neoadjuvant chemotherapy
- loop mediated isothermal amplification
- newly diagnosed
- iron oxide nanoparticles
- label free
- real time pcr
- ejection fraction
- patients undergoing
- chronic kidney disease
- case report
- peritoneal dialysis
- clinical trial
- squamous cell carcinoma
- radiation therapy
- systematic review
- living cells
- rectal cancer
- highly efficient
- artificial intelligence
- cross sectional
- platelet rich plasma
- high resolution
- deep learning