Purpose: Purpose: To investigate the clinical therapeutic effect and safety of thalidomide combined with temozolomide (TMZ) and three-dimensional conformal radiotherapy for patients with high-grade gliomas after operation.
Methods: Methods: The clinical data of 108 patients with high-grade gliomas undergoing operation in our hospital from September 2014 to December 2016 were retrospectively analyzed, of which 54 received thalidomide combined with TMZ and three-dimensional conformal radiotherapy (thalidomide group) and 54 received TMZ combined with three-dimensional conformal radiotherapy (control group). The clinical data of all patients were collected, and the short-term therapeutic effect, adverse reactions after treatment and quality of life scores were compared between the two groups of patients. Thereafter, the level of serum immune factors of the patients was recorded, and the overall survival (OS) rate and progression-free survival (PFS) rate of the patients were followed up and recorded.
Results: Results: The therapeutic effect was evaluated in all the patients at 1 month after treatment. It was found that the overall response rate (ORR) in thalidomide group [68.5% (37/54)] was markedly higher than that in control group [44.4% (24/54)] (p=0.012), but the difference in the disease control rate (DCR) between thalidomide group [92.6% (50/54)] and control group [83.3% (45/54)] was not statistically significant (p=0.139). After treatment, the scores of 36-Item Short Form Health Survey (SF-36) evaluating the quality of life in thalidomide group were higher than that in control group, in which the physical function score was statistically significantly different between the two groups (p=0.028), whereas the scores of the other items did not statistically significantly differ between the two groups (p>0.05). Following treatment, the levels of serum hepatocyte growth factor (HGF), tumor necrosis factor-alpha (TNF-α), interleukin (IL)-6, IL-17, vascular endothelial growth factor (VEGF) and epidermal growth factor (EGF) were remarkably reduced in the two groups of patients, and these indexes in thalidomide group were lower than those in control group after treatment. Among them, HGF (p=0.069), TNF-α (p=0.076), IL-6 (p=0.149) and IL-17 (p=0.114) showed no statistically significant differences, but VEGF and EGF were statistically significantly different between the two groups (p<0.001). Moreover, adverse reactions were mainly manifested as myelosuppression, nausea and vomiting, constipation, liver function injury, drowsiness and neurotoxicity (grade I-II in most cases), which returned to normal after symptomatic treatment. Besides, the incidence rate of drowsiness of the patients in thalidomide group was notably lower than that in control group (p=0.029), but the difference in the incidence rate of other manifestations was not statistically significant (p>0.05). Additionally, the follow-up results manifested that the median OS was (16.1±3.6) months, (12.8±3.9) months, respectively, and the median PFS was (9.0±3.2) months and (12.3±3.4) months, respectively, in thalidomide group and control group. Furthermore, log-rank test revealed that the patients in thalidomide group had longer OS (p=0.025) and PFS (p=0.040) than those in control group.
Conclusions: Conclusions: The application of thalidomide combined with TMZ and three-dimensional conformal radiotherapy for high-grade glioma patients after operation can prominently enhance the clinical therapeutic effect, improve patient quality of life, prolong survival, and produce tolerable adverse reactions.
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Lancet Haematol
January 2025
University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Background: In CARTITUDE-4, ciltacabtagene autoleucel (cilta-cel) significantly improved progression-free survival (primary endpoint; previously reported) versus standard of care in patients with relapsed, lenalidomide-refractory multiple myeloma. We report here patient-reported outcomes.
Methods: In the ongoing, phase 3, open-label CARTITUDE-4 study, patients were recruited from 81 sites in the USA, Europe, Asia, and Australia, and were randomly assigned 1:1 to cilta-cel (target, 0·75 × 10 CAR-T cells/kg) or standard of care (daratumumab, pomalidomide, and dexamethasone; pomalidomide, bortezomib, and dexamethasone).
Sci Rep
December 2024
Department of Anesthesiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Sepsis is defined as a dysfunctional, life-threatening response to infection leading to multiorgan dysfunction and failure. During the past decade, studies have highlighted the relationship between sepsis and aging. However, the role of aging-related mechanisms in the progression and prognosis of sepsis remains unclear.
View Article and Find Full Text PDFImmun Inflamm Dis
December 2024
Department of Rheumatology and Immunology, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Objective: This study aimed to investigate the efficacy and safety of a triple therapy consisting of colchicine, thalidomide and total glucosides of paeony (TGP) in Behcet's disease (BD) patients with mucocutaneous involvement.
Methods: Totally 355 newly diagnosed BD patients with mucocutaneous involvement were recruited, who received dexamethasone and colchicine for the first 2 weeks, then they were categorized into "sustained triple-therapy (ST)" (n = 231) and "colchicine to triple-therapy (CT)" (n = 124) groups respectively: for ST group, patients received colchicine, thalidomide plus TGP from Month (M)0.5 to M12; for CT group, patients received colchicine from M0.
EJHaem
December 2024
Johnson & Johnson Innovative Medicine Lisbon Portugal.
Objectives: To characterize variations in real-world treatment patterns in multiple myeloma (MM) in Portugal over a 5-year period.
Methods: A retrospective cohort multicenter study using secondary data of national hospital drug consumption database from 11 Portuguese public hospitals between 2017 and 2022.
Results: Number of MM-treated patients increased 53% over 5 years (from 825 to 1266 patients).
Arch Dermatol Res
December 2024
Department of Dermatology, Venereology and Leprology, Mahatma Gandhi Medical College and Hospital, Jaipur, Rajasthan, India.
Introduction: Alopecia areata (AA) is a chronic, immune-mediated inflammatory disorder characterized by nonscarring hair loss. The management of AA poses challenges due to its unpredictable course and variable response to treatment. In this comparative study, we evaluated the efficacy and safety of oral apremilast, intralesional corticosteroids (ILC) and a combination of both in patients with patchy AA.
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