Archives of Gynecology and Obstetrics, Год журнала: 2024, Номер unknown
Опубликована: Окт. 16, 2024
Язык: Английский
Archives of Gynecology and Obstetrics, Год журнала: 2024, Номер unknown
Опубликована: Окт. 16, 2024
Язык: Английский
Journal of Gastrointestinal Cancer, Год журнала: 2025, Номер 56(1)
Опубликована: Янв. 20, 2025
Язык: Английский
Процитировано
1Clinical Oncology, Год журнала: 2024, Номер 36(10), С. e408 - e419
Опубликована: Июль 2, 2024
Язык: Английский
Процитировано
5European Journal of Clinical Pharmacology, Год журнала: 2024, Номер unknown
Опубликована: Ноя. 14, 2024
Язык: Английский
Процитировано
4Expert Review of Anticancer Therapy, Год журнала: 2025, Номер unknown
Опубликована: Янв. 28, 2025
Background Immune checkpoint inhibitors (ICIs) are currently the primary approach for managing NSCLC. However, numerous combination therapies under investigation. Our goal is to investigate overall efficacy and safety of ICIs taxane-based chemotherapy.
Язык: Английский
Процитировано
0Frontiers in Immunology, Год журнала: 2025, Номер 16
Опубликована: Янв. 31, 2025
The combination of programmed cell death 1 (PD-1)/programmed ligand (PD-L1) inhibitors with chemotherapy (CT) is currently under evaluation as a first-line treatment for advanced or recurrent endometrial cancer (EC). This study sought to assess the efficacy and safety this therapeutic in patients EC. We performed an exhaustive review randomized controlled trials (RCTs) up September 25, 2024, examining combining PD-1/PD-L1 CT versus alone (or plus placebo) Efficacy was measured by progression-free survival (PFS) overall (OS), while assessed incidence any grade ≥ 3 adverse events (AEs). calculated hazard ratios (HRs) PFS OS, well risk (RRs) AEs, each accompanied 95% confidence intervals (CIs). To evaluate heterogeneity, we employed Cochran's Q test, I2 statistics, prediction (PIs). Trial sequential analysis (TSA) conducted using R Version 4.3.1, STATA 12.0, TSA 0.9.5.10 Beta software. Our incorporated 6 studies, encompassing total 2,954 patients. significantly improved (HR = 0.617, CI: 0.506-0.752; PI: 0.334-1.140) OS 0.774, 0.664-0.902; 0.553-1.083) compared population. Subgroup based on mismatch repair (MMR) status revealed pronounced benefits deficient MMR (dMMR) (PFS: HR 0.344, 0.269-0.438; 0.231-0.510; OS: 0.371, 0.245-0.562; 0.025-5.461) those proficient (pMMR) 0.772, 0.627-0.950; 0.394-1.512; 0.996, 0.692-1.435; 0.021-47.662). Although there no observed difference grades AEs (RR 0.994, 0.982-1.006; 0.978-1.009), elevated group receiving 1.132, 1.023-1.252; 0.836-1.532). EC patients, particularly dMMR. Clinicians can tailor strategies according individual patient characteristics optimize outcomes, remaining alert possibility clinical practice. https://www.crd.york.ac.uk/PROSPERO/, identifier CRD42024595455.
Язык: Английский
Процитировано
0Microbial Pathogenesis, Год журнала: 2025, Номер unknown, С. 107407 - 107407
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
0Journal of Chemotherapy, Год журнала: 2025, Номер unknown, С. 1 - 7
Опубликована: Фев. 21, 2025
The incidence of endometrial cancer (EC), a widely prevalent gynecological malignancy, is witnessing global surge. Although early-stage demonstrates promising outcomes, advanced associated with an unfavorable prognosis. Nevertheless, for specific pathological types or molecular subtypes EC, accurate treatment algorithm can lead to favorable Here, we report case stage IVB EC characterized by mucinous differentiation mismatch repair deficiencies (MMRd) who was successfully treated combination oxaliplatin and programmed cell death protein 1 (PD-1) inhibitor. Our findings emphasize the importance conducting typing assessments in individuals recurrent EC. Additionally, combining PD-1 inhibitors may be viable option MMRd. More representative standardized studies are needed consolidate this conclusion.
Язык: Английский
Процитировано
0International Journal of Gynecological Cancer, Год журнала: 2025, Номер unknown, С. 101759 - 101759
Опубликована: Март 1, 2025
ObjectivePD-(L)1 inhibitors have shown benefit in mismatch repair-deficient (MMRd) endometrial cancer. However, their efficacy MMR-proficient cancer — comprising POLE-mutated (POLEmut), p53-abnormal (p53abn), and no-specific-molecular-profile (NSMP) molecular classes remains unclear. This systematic review meta-analysis evaluated the of PD-(L)1 inhibitors, as monotherapy or combined with chemotherapy, across four classes.MethodsSystematic searches were conducted Embase, PubMed, Cochrane, Web Science, manual reference lists conference websites. Seven reports on five clinical trials identified, three included meta-analysis. Overall survival progression-free assessed.ResultsIn patients primary advanced recurrent MMRd (n=215), adding a inhibitor to platinum-based chemotherapy significantly improved overall (HR: 0.36, 95% CI: 0.21─0.62) 0.35, 0.23─0.53). In p53abn cancer, significant was observed 0.71, 0.53–0.94; n=326), but no 0.80, 0.34–1.84; n=135). NSMP benefits for 0.97, 0.39–2.43; n=242) 0.44–1.44; n=373), latter affected by heterogeneity. Insufficient data available POLEmut (n=12), events reported two out majority (n=11).ConclusionPD-(L)1 inhibition demonstrated showed potential benefit, while such not found. although rare metastatic settings, associated favorable prognosis regardless treatment. These findings underscore relevance classification highlight importance prioritizing analyses guide personalized strategies.
Язык: Английский
Процитировано
0BMC Cancer, Год журнала: 2024, Номер 24(1)
Опубликована: Ноя. 6, 2024
Merkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine skin cancer characterized by high rates of metastasis. Emerging evidence suggests that PD-L1/PD1 blockade holds promise as therapeutic option for MCC. However, the efficacy safety this approach in treating MCC remain incompletely understood. This systematic review meta-analysis aims to analyze PD-1/PD-L1 patients with PubMed, Cochrane, Embase were searched studies evaluating undergoing treatment. The estimated outcomes overall response rate (ORR), disease control (DCR), progression-free survival (PFS), (OS), treatment-related adverse events (TRAEs). We performed using RStudio v4.4.2 software. A total 14 reports 13 different encompassing 615 included. median age ranged from 64 77 years. Median follow-up 7.9 months 59.3 months. Pooled OS at 24 36 65.05% (95% CI 44.04–81.49) 59.58% 39.62–76.81), respectively, while pooled PFS 6, 12, 51.78% 37.83–65.45), 46.12% 29.44–63.72), 28.73% 16.57–45.02), same order. DCR proportion was 61.65% 54.85–68.03) ORR 53.79% 47.80-59.68). frequency TRAEs any grade 61.72% 45.75–75.51) ≥ 3 17.60% 12.28 24.57). revealed treatment PD-1/PDL-1 showed durable responses continuous clinically meaningful outcomes.
Язык: Английский
Процитировано
3BMC Cancer, Год журнала: 2024, Номер 24(1)
Опубликована: Июнь 10, 2024
Язык: Английский
Процитировано
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