The aim of our study was to evaluate the efficacy and tolerance of 223RaCl2 in patients with mCRPC with bone metastases, then analyse the impact of any change in treatment protocol on the efficacy of 223RaCl2 in mCRPC patients with bone metastases, by determining overall survival, progression-free survival and events occurring during therapeutic monitoring.
Our retrospective, analytical and descriptive study, carried out in Luxembourg, included patients eligible for le 223RaCl2 treatment who were assessed during and at the end of treatment, and 3 to 4 months after the end of treatment.
Our sample included 41 cases. The mean age of patients was 74 years (min = 52, max = 87), with 32 (78.1%) deaths recorded. Median overall survival was 18.0 months (95% CI: 12.1–23.9): 11 months for those who experienced progression during treatment versus 47 months for those who experienced a partial response. Median progression-free survival was 15.0 months (95% CI: 0.0–36.4). Overall survival was positively correlated with progression-free survival (Rho Spearman = 0.713, P-value < 0.001); however, a one-month increase in progression-free survival decreased the risk of death by 6% and thus increased overall survival (HR = 0.937, 95% CI : 0.903–0.973, P < 0.001).
Administration of the complete 223RaCl2 protocol improved overall survival and progression-free survival in patients treated for mCRPC with bone metastases, with good hematological tolerability despite the occurrence of complications such as epiduritis and fractures.
To assess the utility of metabolic parameters obtained from baseline and post-neoadjuvant chemotherapy (NAC) 18F FDG PET/CT scans in predicting postoperative residual cancer burden (RCB) scores in locally-advanced breast cancer (LABC).
In our retrospective study, we enrolled 58 LABC patients who underwent baseline and post-treatment 18F FDG PET/CT scans followed by surgery between June 2020 and February 2022. Patients were categorized by their molecular subtypes as Luminal groupe (Luminal A and Luminal B (HER 2 negative)), HER2 positive and triple-negative (TN). We recorded various metabolic parameters, including maximum standardized uptake value (SUVmax), mean SUV (SUVmean), metabolic tumor volume (MTV), total lesion glycolysis (TLG), maximum standardized uptake lean body mass (SULmax), and mean SUV lean body mass (SULmean) of the primary tumor (T). To minimize the effect of SUV changes between PET studies, SUV ratios of tumor and liver were recorded for each study as TLR1 and TLR2 respectively. We calculated the percent reduction in SUVmax (ΔSUVmax%) between 2 PET studies. Patients were categorized into two groups based on postoperative RCB scores: RCB0/I (pathological responders, pR) and RCB II/III (pathological non-responders, non-pR).
Twenty-six patients (44.8%) were pR and 32 (55.2%) were non-pR. Baseline metabolic parameters were similar in 2 groups. Post-treatment T SUVmax2, T SUVmean2, T SULmax2, T SULmean2, TLR SUV2, and TLR SUL2 values were significantly different between the pR and non-pR patients across all molecular subgroups. Also, pR patients exhibited a significantly higher mean ΔSUVmax compared to non-pR patients. In the Luminal and HER2 positive groups, T SUVmax2 and T SUVmean2 values successfully discriminated the pR and non-pR groups with high accuracy, achieving 100% sensitivity and 100% specificity in the luminal group. In the luminal group, a −75.4% cut-off value for ΔSUVmax predicted pR with 100% sensitivity.
Our findings indicate that SUV parameters, normalized to lean body mass as recommended by PERCIST, can be valuable for the early non-invasive prediction of pR and non-pR patients using post-NAC 18F FDG PET/CT.
An extensive tumor thrombus is an extremely rare entity in thyroid cancer. It is related to aggressive tumor behavior and a poorer prognosis. 18F-FDG PET is a useful tool for accurate staging and restaging in malignancies as well as the determination of tumor thrombus and its differential diagnosis from benign thromboembolism. We report a rare case of 66-year-old patient with an extensive tumor thrombus in superior vena cava on 18F-FDG PET/CT.
Fluorodeoxyglucose (FDG) 18F-FDG PET/CT plays an important role in lymphoma staging and evaluation of treatment response. Mimics should be considered when evaluating 18F-FDG PET/CT images to perform correct staging and correct treatment response evaluation. Splenosis is one of the causes that may cause misinterpretation by mixing with lymph nodes in lymphoma patients. In our case report, we visualized splenosis mimicking lymph node in a 50-year-old lymphoma patient with 99mTc nano-colloid scintigraphy.
For 15 years, regadenoson, a selective adenosine 2A (A2A) receptor agonist, has been largely used as a pharmacologic stress agent in myocardial perfusion studies. It acts by increasing coronary blood flow. It has been shown to be non-inferior to adenosine for the detection of reversible myocardial ischemia. Regadenoson has several advantages, including less serious adverse effects, better tolerance and easier practical administration. However, specific adverse effects on the central nervous system, although rarely reported, can provocoke seizure through A2A receptor activation. We report here a case of regadenoson-associated-seizure and review the relevant literature. A 73-year-old male with a past medical history of hypertension, atrial fibrillation, stroke, hemodialysis and type 2 diabetes was referred for evaluation of hypokinesia of the apical segments. He had an unique episode of epilepsia in 2008. Less than one minute after regadenoson injection, he had a partial tonic-clonic seizure of the right upper and lower limbs, which lasted for 30 seconds and resolved spontaneously. This case report is a reminder that this under-diagnosed adverse effect must be taken into consideration when using regadenoson for cardiac stress testing.