Publications by authors named "Lujin Li"

Objectives: This study aimed to quantitatively evaluate the efficacy and safety of first-line systemic therapies for treating advanced hepatocellular carcinoma (aHCC).

Methods: The study included clinical trials of first-line systemic therapies for aHCC since the approval of sorafenib in 2007. Hazard function models were used to describe changes in overall survival (OS) and progression-free survival (PFS) over time.

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  • - The text discusses Non-alcoholic fatty liver disease (NAFLD), recently called metabolic dysfunction-associated steatotic liver disease (MASLD), which affects about 30% of the global population and currently lacks optimal treatment options.
  • - The objective is to assess the effects of vitamin E, both alone and in combination with other vitamins or minerals, compared to placebo on individuals with NAFLD, using rigorous guidelines for selecting clinical trials.
  • - The study evaluates various outcomes, focusing on mortality rates and serious health impacts while also assessing the risk of bias and the quality of evidence through established Cochrane research methods.
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  • This study evaluates when exercise is most effective in treating osteoarthritis (OA) symptoms and how different types of exercise impact these symptoms.
  • It uses data from various databases to analyze randomized controlled trials that focus on the effects of exercise on knee, hip, or hand OA.
  • Results show that exercise effectiveness peaks between 1.6 to 7.2 weeks after starting, with local exercise techniques proving to be the most beneficial in reducing pain and improving function.
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  • Pyrazinamide is used to treat both drug-susceptible and multidrug-resistant tuberculosis, and this study looks at factors affecting its pharmacokinetics to improve dosing strategies.
  • A population pharmacokinetic model was developed using data from 222 patients in China, revealing that total body weight significantly impacts the drug's clearance.
  • Recommendations for fixed dosages based on patient weight were established, suggesting doses of 1500 mg for those weighing 40-70 kg, 1750 mg for 70-80 kg, and 2000 mg for 80-90 kg to ensure effective treatment outcomes.
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Consumption of herbal products containing pyrrolizidine alkaloids (PAs) is one of the major causes for hepatic sinusoidal obstruction syndrome (HSOS), a deadly liver disease. However, the crucial metabolic variation and biomarkers which can reflect these changes remain amphibious and thus to result in a lack of effective prevention, diagnosis and treatments against this disease. The aim of the study was to determine the impact of HSOS caused by PA exposure, and to translate metabolomics-derived biomarkers to the mechanism.

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Background: Amyotrophic lateral sclerosis (ALS) is an irreversible degenerative disease. Placebo-controlled randomized trials are currently the main trial design to assess the clinical efficacy of drugs for ALS treatment. The aim of this study was to establish models to quantitatively describe the course of ALS, explore influencing factors, and provide the necessary information for ALS drug development.

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Background: Further dose optimization is required for patients with moderate-to-severe plaque psoriasis who do not benefit from the approved secukinumab dose regimen. This study aimed to develop an exposure-response model for secukinumab to recommend dose regimens for patients of different body weights.

Methods: We searched the PubMed and Cochrane Library databases for randomized controlled trials using PASI 75 and PASI 90 response rates as primary outcomes.

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Objectives: This study aimed to quantitatively compare the efficacy and safety of long-acting β-agonist (LABA)/long-acting muscarinic antagonist (LAMA) and LABA/inhaled corticosteroid (ICS) fixed-dose combinations (FDCs) in preventing moderate or severe chronic obstructive pulmonary disease (COPD) exacerbations.

Methods: A literature search was performed using public databases. The time course characteristics of the probability of a moderate or severe exacerbation in stable COPD patients treated with LABA/LAMA and LABA/ICS FDCs were described by the parametric survival function.

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  • Wendan decoction (WDD) is a traditional Chinese remedy for depression with limited high-quality evidence supporting its efficacy, prompting a study to evaluate its clinical effectiveness using a novel external control method.
  • The study analyzed data from 5 clinical trials involving 177 participants, finding that WDD had a slow onset but a significant rate of improvement in depression symptoms after 8 weeks, comparable to some conventional antidepressants.
  • The findings suggest that WDD has potential as a treatment for depression and indicate a need for larger randomized controlled trials to further verify its effectiveness.
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This study quantified the differences in the efficacy and safety of different stimulation domains of anti-CD19 chimeric antigen receptor (CAR) T therapy for B-cell acute lymphoblastic leukemia (B-ALL). Clinical trials related to anti-CD19 CAR T-cell therapy for B-ALL were searched in public databases from database inception to 13 November 2021. The differences in overall survival (OS) and progression-free survival (PFS) of B-ALL patients treated with anti-CAR T-cell therapy containing 4-1BB and CD28 co-stimulatory domains were compared by establishing a parametric survival function.

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  • The study evaluates the effectiveness of various drugs and a placebo in treating primary progressive multiple sclerosis (PPMS) through a quantitative analysis of existing clinical trials.
  • A total of 15 studies with 3779 patients were analyzed, identifying 12 drugs; while some drugs showed similar efficacy to placebo, others, particularly ocrelizumab, demonstrated significantly better outcomes.
  • The findings contribute valuable data for informed clinical decisions regarding PPMS treatment and guide future clinical research.
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Objective: While platelet rich plasma (PRP) has been extensively studied in treating osteoarthritis (OA), there has been an ongoing debate regarding the efficacy of PRP and the optimal subpopulation for PRP treatment remains unknown. The authors hereby aim to establish a pharmacodynamic model-based meta-analysis to quantitatively evaluate PRP efficacy, comparing with hyaluronic acid (HA) and identify relevant factors that significantly affect the efficacy of PRP treatment for OA.

Methods: The authors searched for PubMed and the Cochrane Library Central Register of Controlled Trials of PRP randomized controlled trials (RCTs) for the treatment of symptomatic or radiographic OA from the inception dates to 15 July 2022.

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New therapies for relapsed/refractory diffuse large B-cell lymphoma (r/rDLBCL) have emerged in recent years, but there have been no comprehensive quantitative comparisons of the efficacy of these therapies. In this study, the efficacy characteristics of 11 types of treatment strategy and 63 treatment regimens were compared by model based meta-analysis. We found that compared with monotherapy, association therapy had significant benefits in terms of overall survival (OS), progression-free survival (PFS), and objective response rate (ORR).

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Importance: In osteoarthritis (OA) clinical trials, a placebo is often used as control. Therefore, a thorough understanding of the placebo response is important for guiding drug development in OA.

Objective: To develop an oral placebo response model for OA.

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  • * A population pharmacokinetic model was created using data from 99 Chinese adult MDR-TB patients, showing that the drug follows a one-compartment model with first-order absorption.
  • * The study found that certain genetic factors (specifically the SNP rs319952) and liver enzyme levels (GGT) significantly affect the drug's clearance, which can guide personalized dosing for better treatment outcomes.
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The purpose of this study was to quantify the efficacies and safety profiles of the three first-line non-platinum chemotherapy regimens recommended in the National Comprehensive Cancer Network guidelines. The PubMed and Cochrane Library databases were searched comprehensively, and clinical trials involving patients with advanced non-small cell lung cancer treated with one of three first-line non-platinum regimens (gemcitabine combined with vinorelbine, gemcitabine combined with docetaxel, or gemcitabine alone) were included in the analysis. A parametric proportional hazard survival model was established to analyze the time course of overall survival (OS).

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  • Neuromyelitis optica spectrum disorders (NMOSD) is a disease that affects the central nervous system and this study compared seven different drugs to see which one is most effective at preventing relapses.
  • A total of 24 clinical trials involving 2207 patients were analyzed, focusing on the "time to first relapse" after treatment to determine the long-term effects of each drug.
  • The results indicated that eculizumab was the most effective, with 98.9% of patients remaining relapse-free at 24 months, providing valuable data for future clinical practice and research.
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Background: The GINA recommends inhaled corticosteroids (ICSs) for the treatment of steps 2-3 of childhood asthma. However, the difference in efficacy between these drugs remains unclear. The purpose of this study was to compare the efficacy of different ICS drugs in the treatment of childhood asthma.

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Introduction: There is a wide variety of drugs for the clinical treatment of immunoglobulin A (IgA) nephropathy; however, previous studies have failed to clarify the quantitative differences in the efficacy of various drugs. In this study, we aimed to quantitatively compare the clinical efficacy of 6 classes of drugs with different pharmacological mechanisms for the treatment of IgA nephropathy and to identify relevant influencing factors.

Methods: Clinical trials of drugs for the treatment of IgA nephropathy were obtained from public databases.

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What Is Known And Objectives: Gemcitabine combined with platinum is currently the recommended first-line chemotherapy for advanced non-small cell lung cancer (NSCLC). This study aimed to quantitatively compare the efficacy and safety of gemcitabine-platinum combinations in the treatment of advanced NSCLC under different dosing regimens based on extensive literature data.

Methods: The PubMed and Cochrane Library databases were systematically searched for clinical trials in patients with NSCLC treated with a gemcitabine-platinum regimen.

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This study used model analysis to clarify the benefits and risks of postoperative adjuvant chemotherapy compared with surgery alone in patients with stage II/III colorectal cancer. Clinical trials involving patients with stage II/III colorectal cancer who underwent surgery alone or those who received post-surgical adjuvant chemotherapy were searched in the PubMed and embase databases. By establishing a survival model, the overall survival (OS) and disease-free survival (DFS) of patients who underwent surgery alone or postoperative adjuvant chemotherapy were quantitatively analyzed to compare the differences between the two.

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  • Tacrolimus is used in organ transplantation to prevent rejection, but its dosing is complicated due to its narrow therapeutic window and variability among patients.
  • This study developed a population pharmacokinetic model specifically for Chinese liver transplant patients, analyzing factors that affect tacrolimus clearance.
  • The final model identified demographic factors, genetic differences (especially CYP3A5), drug combinations (like Wuzhi Capsule and corticosteroids), and post-operative days as key elements that should be considered for individualizing tacrolimus dosing.
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  • This study compared the effectiveness of two asthma medications, fluticasone furoate (FF) and fluticasone propionate (FP), in adolescents and adults by analyzing 14 placebo-controlled trials with a total of 6640 participants.
  • The results showed that both medications reached their maximum efficacy within two weeks, with FF showing slightly better improvement in lung function (measured as FEV) compared to FP at evaluated doses.
  • Additionally, while both drugs had similar effects on asthma symptoms and quality of life when compared to placebo, FP reached its maximum effect at the highest dose, whereas FF did not, indicating potential differences in how these medications work.
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Objective: This study aimed to quantitatively compare the efficacy and safety of long-acting β2-agonist (LABA)/long-acting muscarinic antagonist (LAMA) fixed-dose combinations (FDCs) for the treatment of stable chronic obstructive pulmonary disease (COPD), especially in terms of their loss of efficacy in lung function.

Methods: Randomized controlled clinical trials of LABA/LAMA FDCs for the treatment of stable COPD were comprehensively searched for in public databases. Pharmacodynamic models were established to describe the time course of the primary outcome [trough forced expiratory volume in the first second (FEV)].

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Purpose: The risk of sudden cardiac death in patients receiving atypical antipsychotics may be related to QTc prolongation. The aim of this study was to investigate the risk factors for QTc prolongation to prevent QTc prolongation and guide clinical practice.

Methods: All electrocardiogram recordings of 913 schizophrenia patients who were receiving atypical antipsychotics were reviewed for prolonged QTc and associated conditions.

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