The aim of our study was to explore the effect of IORT on survival outcome of patients with musculoskeletal malignancy. The prognostic factors of patients with IORT treatment were also identified in this study. The retrospective analysis was conducted based on the Surveillance, Epidemiology, and End Results (SEER) database spanning from 2000 to 2020. The musculoskeletal malignancy patients who received both surgery and radiation therapy (RT) treatment were included into the study. Survival differences between groups were explored by Kaplan-Meier method and log-rank test. Potential prognostic factors of patients with IORT treatment were identified by Cox proportional hazards regression analysis. A total of 24,297 patients were selected finally, including 23,877 cases with neoadjuvant/adjuvant RT alone, 190 cases with IORT alone, and other 230 cases received both neoadjuvant/adjuvant RT and IORT. The median survival time of these patients was 141.0 (95%CI: 101.1-180.9) months. Patients who received both IORT and neoadjuvant/adjuvant RT treatment presented the best survival outcome when compared with those underwent either IORT or neoadjuvant/adjuvant RT only. Further subgroup analyses verified the survival benefit of the combination of IORT and neoadjuvant/adjuvant RT in female patients with tumor located on limb and in patients who received the performance of chemotherapy. A series of variables, including age at diagnosis, gender, primary tumor site, tumor Grade, SEER stage, T stage, N stage, IORT only or the combination of IORT and neoadjuvant/adjuvant RT, the performance of chemotherapy, were identified as independent prognostic factors of patients with IORT treatment. The current study is distinguished by its large-scale analysis of the SEER database, encompassing a comprehensive cohort of musculoskeletal malignancy patients treated with IORT, as well as the rigorous subgroup analysis. We concluded that IORT during surgery procedure, accompanied with neoadjuvant/adjuvant RT, might confer a survival benefit for selected patients diagnosed with musculoskeletal malignancy.
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http://dx.doi.org/10.7150/jca.100678 | DOI Listing |
Clin Case Rep
January 2025
Los Angeles, David Geffen School of Medicine, Department of Anesthesiology and Perioperative Medicine, Division of Pain Medicine University of California Los Angeles California USA.
Heightened clinical vigilance for multiple myeloma is essential in patients presenting with atypical chronic pain progression. Symptoms may overlap with degenerative musculoskeletal conditions, frequently leading to misdiagnosis. This underscores the necessity of a thorough evaluation when symptoms are refractory to conventional therapies, in order to facilitate timely diagnosis and effective management of malignancy.
View Article and Find Full Text PDFEpigenetics Chromatin
January 2025
Department of Molecular Biology, Semmelweis University, Budapest, Hungary.
DNA methylation, catalyzed by DNA methyltransferases (DNMT), plays pivotal role in regulating embryonic development, gene expression, adaption to environmental stress, and maintaining genome integrity. DNMT family consists of DNMT1, DNMT3A, DNMT3B, and the enzymatically inactive DNMT3L. DNMT3A and DNMT3B establish novel methylation patterns maintained by DNMT1 during replication.
View Article and Find Full Text PDFJ Cachexia Sarcopenia Muscle
February 2025
Department of Physical Therapy, University of Florida Health Cancer Center, Gainesville, Florida, USA.
Background: Cancer cachexia represents a debilitating muscle wasting condition that is highly prevalent in gastrointestinal cancers, including pancreatic ductal adenocarcinoma (PDAC). Cachexia is estimated to contribute to ~30% of cancer-related deaths, with deterioration of respiratory muscles suspected to be a key contributor to cachexia-associated morbidity and mortality. In recent studies, we identified fibrotic remodelling of respiratory accessory muscles as a key feature of human PDAC cachexia.
View Article and Find Full Text PDFCurr Obes Rep
January 2025
Maine Medical Center Research Institute, Maine Medical Center, 81 Research Drive, Scarborough, ME, 04074, USA.
Purpose Of Review: Bone marrow adipose tissue is a distinctive fat depot located within the skeleton, with the potential to influence both local and systemic metabolic processes. Although significant strides have been made in understanding bone marrow adipose tissue over the past decade, many questions remain regarding their precise lineage and functional roles.
Recent Findings: Recent studies have highlighted bone marrow adipose tissue's involvement in continuous cross-talk with other organs and systems, exerting both endocrine and paracrine functions that play a crucial role in metabolic homeostasis, skeletal remodeling, hematopoiesis, and the progression of bone metastases.
Cell Commun Signal
January 2025
Department of Musculoskeletal Tumor, Peking University People's Hospital, No. 11 Xizhimen South Street, Beijing, 100044, China.
Background: Ewing's sarcoma (EwS), a common pediatric bone cancer, is associated with poor survival due to a lack of therapeutic targets for immunotherapy or targeted therapy. Therefore, more effective treatment options are urgently needed.
Methods: Since novel immunotherapies may address this need, we performed an integrative analysis involving single-cell RNA sequencing, cell function experiments, and humanized models to dissect the immunoregulatory interactions in EwS and identify strategies for optimizing immunotherapeutic efficacy.
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