Objectives: To investigate the frequency and patterns of calcification in ovarian tumours and evaluate their association with various histological types and malignancy grades.
Methods: This retrospective study included patients who underwent non-contrast CT between March 2015 and March 2024 and had pathologically confirmed ovarian tumours. CT scans were reviewed for the presence and patterns of calcification (punctate, linear, coarse, and amorphous) by three radiologists. Statistical analysis was performed using the Fisher-Freeman-Halton exact test with Bonferroni correction.
Results: This study included 328 patients (mean age, 55 years; range, 18-88 years). Significant differences in calcification frequency were observed among major tumour categories (p < 0.001), with with germ cell tumours being more calcified and metastases less calcified. Similarly, a significant difference was also found among epithelial tumours (p = 0.005), where mucinous and Brenner tumours were more calcified, whereas serous tumours were less calcified. Benign epithelial tumours showed a significantly higher frequency of calcification than borderline tumours and carcinomas (p < 0.001). When comparing the calcification patterns observed among epithelial tumours, significant differences were found for all calcification patterns: punctate (p = 0.024), linear (p < 0.001), coarse (p < 0.001), and amorphous (p < 0.001). The linear pattern was more common in mucinous tumours, whereas the amorphous pattern was more common in serous and Brenner tumours. Among non-epithelial tumours, germ cell tumours frequently exhibited liner and many calcifications, and immature teratomas were characterised by a mixture of punctate, linear, and coarse calcifications. Granulosa cells and metastatic tumours did not exhibit calcification.
Conclusions: Among epithelial tumours, mucinous and Brenner tumours had a significantly higher frequency of calcification, and benign tumours had a significantly higher frequency of calcification. Amorphous patterns were significantly more common in serous and Brenner tumours, while linear patterns were significantly more common in mucinous tumours.
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http://dx.doi.org/10.1007/s11604-025-01750-4 | DOI Listing |
Sci Transl Med
March 2025
Cancer Biology Research Center (Key Laboratory of the Ministry of Education), Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430000, China.
The benefit of hyperthermic intraperitoneal chemotherapy (HIPEC) in ovarian cancer remains controversial, hindering the development of rational combination therapies based on hyperthermia (HT). This study reports the preliminary results of the neoadjuvant HIPEC (NHIPEC) trial (ChiCTR2000038173), demonstrating enhanced tumor response in high-grade serous ovarian cancer with NHIPEC. Through single-cell RNA sequencing analysis, we identified both homogeneous and heterogeneous cellular responses to HT within the tumor and microenvironment.
View Article and Find Full Text PDFCancer
March 2025
Department of Oncology, Karmanos Cancer Institute at Wayne State University, Detroit, Michigan, USA.
Background: Prior studies of participants with breast and other obesity-associated cancers in the Women's Health Initiative (WHI) showed worse mortality and cardiovascular disease (CVD) outcomes for individuals with a higher number of cardiometabolic risk factors at study entry. The purpose of this analysis is to compare the relationship between cardiometabolic abnormalities and mortality among women with and without cancer in the WHI.
Methods: Women with one of five early-stage obesity-associated cancers (breast, colorectal, endometrial, ovarian, and non-Hodgkin lymphoma) and controls without any new or prior history of cancer were selected from the WHI-Life and Longevity after Cancer ancillary study.
Cells
March 2025
Department of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Ovarian cancer survival depends strongly on the time of diagnosis. Detection at stage 1 must be the goal of liquid biopsies for ovarian cancer detection. We report the development and validation of graphene-based optical nanobiosensors (G-NBSs) that quantify the activities of a panel of proteases, which were selected to provide a crowd response that is specific for ovarian cancer.
View Article and Find Full Text PDFCells
March 2025
Department of Structural and Functional Biology, Institute of Biosciences, São Paulo State University (Unesp), Botucatu 18618-689, São Paulo, Brazil.
Ovarian cancer (OC) is characterized by high mortality rates due to late diagnosis, recurrence, and metastasis. Here, we show that extracellular signaling molecules secreted by adipose-derived mesenchymal stem cells (ASCs) and OC cells-either in the conditioned medium (CM) or within small extracellular vesicles (sEVs)-modulate cellular responses and drive OC progression. ASC-derived sEVs and CM secretome promoted OC cell colony formation, invasion, and migration while upregulating tumor-associated signaling pathways, including TGFβ/Smad, p38MAPK/ERK1/2, Wnt/β-catenin, and MMP-9.
View Article and Find Full Text PDFCells
February 2025
Department of Pathology, CHA Bundang Medical Center, CHA University, Seongnam-si 13496, Republic of Korea.
Patient-derived xenograft (PDX) models are powerful tools in cancer research, offering an accurate platform for evaluating cancer treatment efficacy and predicting responsiveness. However, these models necessitate surgical techniques for tumor tissue transplantation and face challenges with non-uniform tumor growth among animals. To address these issues, we attempted to develop a new PDX modeling method using high-grade serous ovarian cancer (HGSC), a fatal disease with a 5-year survival rate of 29%, which requires personalized research due to its morphological, genetic, and molecular heterogeneities.
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