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Efficacy evaluable population

Web30 minutes ago · Patient Population: Median age was 63 (range of 31-77); 78% were male; ... 42 pts were evaluable for efficacy, receiving ≥2 treatment cycles (≥8 weeks) with ≥1 post-baseline tumor assessment ... WebMar 31, 2024 · However, efficacy and safety studies on this population are limited. Nebhan et al. 18 reported that median PFS was 6.7 months and OS was 10.9 months in 345 patients aged ≥80 years. In our study, we enrolled 38 patients ≥80 years of age, and PFS and OS in these patients were comparable to those of the patients aged <80 years old.

History of Changes for Study: NCT03512262 - clinicaltrials.gov

WebMar 10, 2024 · A total of 28 patients have enrolled to the trial, 22 of whom were included in the efficacy-evaluable population. Of the 6 remaining patients who were not included in the efficacy analysis, 1... WebDownload Table Response rates for all evaluable patients (efficacy population: n ¼ 37 patients) from publication: Replacement of bortezomib with carfilzomib for multiple … pinja saikkonen https://calderacom.com

Safety and efficacy of GEMOX plus donafenib and tislelizumab as …

WebApr 11, 2024 · The efficacy analyses were performed in evaluable analysis population, which consisted of patients who received at least one dose of study drugs and had best overall response assessment. ... COVID-19, some patients could not return to the site for follow-up in time, resulting in that only eight patients were evaluable for efficacy. … WebA. Muyle, G. Marais, in Encyclopedia of Evolutionary Biology, 2016 Effects on Effective Population Size. With pure selfing, the effective population size, N e, is decreased by … WebJun 2, 2024 · Results: The efficacy-evaluable cohort comprised 150 adults (vs 121 previously) with 17 different solid tumor types. Median age was 58.5 years; 91% of pts had ECOG PS 0–1 and 37% had received ≥2 prior lines of therapy. Median survival follow-up was 30.6 months. ORR was 61.3% (n = 92/150; 95% CI: 53.1–69.2), including 25 … pinjarra museum

Entrectinib in ROS1 fusion-positive non-small-cell lung cancer ... - PubMed

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Efficacy evaluable population

Safety and Efficacy of Sintilimab and Anlotinib as First Line …

http://www.blackwellpublishing.com/ridley/a-z/Effective_population_size.asp WebDec 12, 2024 · Safety and efficacy of combined ruxolitinib and decitabine in accelerated and blast-phase myeloproliferative neoplasms ... -up. The median overall survival for patients on study was 7.9 months (95% confidence interval, 4.1-not reached). Among evaluable patients, the overall response rate by protocol-defined criteria (complete …

Efficacy evaluable population

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WebOct 26, 2024 · The efficacy-evaluable population consisted of c-Met+ patients (confirmed histology [H]-score ≥ 150) who had at least one postbaseline scan; c-Met+ patients with H-scores ≥ 225 were classified as c-Met high. RESULTS. As of January 2024, 42 patients were enrolled (N = 36 efficacy-evaluable). Neuropathies were the most common any … WebMar 15, 2024 · Within the efficacy evaluable population, the overall response rate was 53% (32/60) with a CR/CRh rate of 30% (18/60), and 78% (14/18) of patients with CR/CRh attaining measurable residual disease (MRD) negativity. The median time to CR/CRh response in the trial was 1.9 months, and the median duration of CR/CRh response was …

WebMay 28, 2024 · Safety population (N = 345) included all pts with NSCLC who received ≥1 selpercatinib dose by data cutoff (30 Mar 2024). Results: In pts with prior treatment (N = … WebApr 18, 2024 · Consequently, in an analysis according to the ITT principle, the original randomization and the number of patients in the treatment groups remain unchanged, …

WebThe efficacy-evaluable population included adult patients (aged ≥18 years) with locally advanced or metastatic ROS1 fusion-positive NSCLC who received entrectinib at a dose of at least 600 mg orally once per day, with at least 12 months' follow-up. All patients had an Eastern Cooperative Oncology Group performance status of 0-2, and previous ... WebMay 31, 2024 · The Kaplan-Meier curves of PFS of unresectable or metastatic hepatocellular carcinoma patients in the efficacy-evaluable population stratified by the presence or absence of immune related-adverse events (irAEs) (A), grade 3 treatment-related adverse events (TRAEs) (B), and baseline controlling nutritional status (CONUT) …

WebMay 3, 2024 · The CR and OR rates will be summarized along with the 2-sided 95% exact Clopper-Pearson confidence interval based on the efficacy evaluable population. Duration of response (DOR) [ Time Frame: Up to 12 months after the CAR-T cell infusion ] Will be assessed among responders.

WebBrief Summary: A 12-month study to measure the efficacy and safety of abaloparatide in men with osteoporosis. Detailed Description: The primary objective of this prospective controlled study is to evaluate the efficacy and the safety of abaloparatide 80 micrograms (mcg) per day administered subcutaneously (SC) compared to placebo in men with … haakjes kapstokWebDec 10, 2024 · As of the March 2024 data cutoff date, 60 patients with R/R mutant NPM1 or KMT2Ar acute leukemia were efficacy evaluable. In the efficacy evaluable population, the ORR was 53% (32/60) with a CR ... pinjarra massageWebDec 11, 2024 · At the data cutoff date for this analysis (May 31, 2024) the efficacy-evaluable population comprised 54 adults with advanced or metastatic NTRK fusion-positive solid tumours comprising ten different tumour types and 19 different histologies. Median follow-up was 12.9 months (IQR 8·77–18·76). 31 (57%; 95% CI 43·2–70·8) of 54 … haaki moviesWebNCI's Dictionary of Cancer Terms provides easy-to-understand definitions for words and phrases related to cancer and medicine. haakkatoenWebNov 14, 2024 · In the efficacy evaluable population of patients who had platinum resistant, measurable disease, and received at least one dose (104 patients), the confirmed ORR … haakjesWebAug 12, 2024 · The most common RET fusion partners in 23 efficacy-evaluable patients were CCDC6 (26%), KIF5B (26%) and NCOA4 (13%). Overall response rate, the primary endpoint, was 57% (95% confidence... haakinsonWebJan 1, 2016 · The Phase 2, 8 mg Tilso/Ipi efficacy evaluable population N=44 (40 with 4 non-evaluable) The Phase 1, 8 mg Tilso/Ipi evaluable population (N=9) Overall … haakinson ameriprise