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1.
China Pharmacy ; (12): 873-878, 2022.
Article in Chinese | WPRIM | ID: wpr-923196

ABSTRACT

OBJECTIVE To exc avate and evaluate the adverse reaction signals of 4 kinds of imported programmed cell death 1 (PD-1)and its ligand (PD-L1)inhibitors,and to guide rational drug use in clinic. METHODS OpenVigil 2.1 software was used to obtain the adverse event reports of four drugs as nivolumab ,pembrolizumab,atezolizumab and durvalumab from the first quarter of 2013 to the fourth quarter of 2020 in the US FDA adverse event reporting system. The reporting odds ratio and proportional reporting ratio were used for signal mining to evaluate new or potential adverse reaction signals. RESULTS A total of 46 840 reports of adverse events with PD- 1/PD-L1 inhibitors as the primary suspected drug were collected ,including 28 896 reports of nivolumab,13 298 reports of pembrolizumab ,3 398 reports of atezolizumab ,and 1 248 reports of durvalumab. From the general characteristics of these reports ,the gender distribution was more men than women ,and the age distribution was mainly in the range of 51-85 years old. The reporting year was mainly in the nearly 4-5 years,and the main reporting countries were the US and Japan,with“death”and“hospitalization or prolonged hospitalization ”as the main serious adverse events which were over 50% of the whole of 4 kinds of adverse events. A total of 1 597 adverse reaction signals were obtained ,involving 26 systems,focusing on “benign,malignant and unspecified neoplasms (cystic and polypoid tumor )”,“infections and infestations ”and“investigations”, etc. The analysis of the top 50 adverse reaction signals showed that the largest number of report was endocrine system disease ,the most frequency signal was “malignant neoplasm progression ”and the strongest adverse reaction signal was “radiation pneumonitis ”. And it was also found that 13 adverse reaction signals ,such as “radiation pneumonitis ”“cholangitis”“fulminant type 1 diabetes mellitus” “blood creatine phosphokinase increased ” “disseminated intravascular coagulation ”“cardiac failure ”and “cerebral infarction ”,etc.,were not reported in the drug instructions. CONCLUSIONS PD-1/PD-L1 inhibitors mediate a large number of adverse reaction signals,resulting in high safety risks in “benign,malignant and unspecified neoplasms (cystic and polypoid tumor )”,“infections and infestations ”and “investigations”,etc. The newly discovered 13 adverse reaction signals ,such as “radiation pneumonitis ”“cholangitis”“blood creatine phosphokinase increased ”“cardiac failure ”and“cerebral infarction ”are of great significance for guiding rational drug use in clinic.

2.
Rev. invest. clín ; 72(4): 231-238, Jul.-Aug. 2020.
Article in English | LILACS | ID: biblio-1251860

ABSTRACT

ABSTRACT Cervical cancer (CC) is one of the most common gynecological tumors and an important health problem, especially in developing countries. The vast majority of patients in early stages are cured of the disease with surgical treatment and with concomitant chemoradiotherapy in locally advanced stages. However, in patients with recurrent, persistent, or metastatic cervical CC, the effectiveness of treatment is limited, except for the combination of chemotherapy based on platinum doublets plus bevacizumab, the treatment that has achieved the best results to date. Programmed cell death-1/PD ligand-1 (PD-1/PD-L1) inhibitors could be a novel and cutting-edge therapeutic option to improve clinical outcomes in this group of patients. Thus far, there are a few Phase I/II clinical trials that have assessed the usefulness of pembrolizumab and nivolumab in this group of patients; these include the KEYNOTE 028, KEYNOTE 158, and CHECKMATE 358 trials, in which clinical benefit has been proven with PD-1/PD-L1 inhibitors in recurrent, persistent, or metastatic CC, as second-line treatment. There are also some ongoing trials that could provide further evidence on the PD-1/PD-L1 pathway as a therapeutic target in CC. In this review, we will focus on the usefulness of these PD-1/PDL1 inhibitors in CC, as well as on trials that are still in the recruitment phase, to confirm their effectiveness in this clinical setting.


Subject(s)
Humans , Female , Uterine Cervical Neoplasms/therapy , B7-H1 Antigen/antagonists & inhibitors , Programmed Cell Death 1 Receptor/antagonists & inhibitors , Immunotherapy , Clinical Trials as Topic , Neoplasm Recurrence, Local
3.
Chinese Journal of Clinical Thoracic and Cardiovascular Surgery ; (12): 953-959, 2020.
Article in Chinese | WPRIM | ID: wpr-824998

ABSTRACT

@#Programmed cell death-1 (PD-1)/programmed cell death-ligand 1 (PD-L1) signaling pathway has been found capable of affecting anti-tumor immune effect in many malignancies in recent years. Patients who are diagnosed with advanced non-small cell lung cancer (NSCLC) have considerable responses after receving inhibitors against PD-1/PD-L1. This paper reviews the clinical progress of PD-1/PD-L1 inhibitors in the treatment of NSCLC.

4.
Acta Academiae Medicinae Sinicae ; (6): 857-865, 2019.
Article in Chinese | WPRIM | ID: wpr-781648

ABSTRACT

Bladder urothelial carcinoma(BUC)is a common malignant tumor in the urinary system.Pt-based chemotherapy has long been a standard therapeutic method for resectable or metastatic BUC,but with poor outcomes.Immune checkpoint inhibitors specific to programmed death 1(PD-1)/programmed death-ligand 1(PD-L1)and cytotoxic T lymphocyte-associated protein 4(CTLA-4)pathways have shown significant antitumor activities,safety,and enduring reactivity in clinical trials,thus creating a new epoch for the treatment of advanced-stage BUC.This article reviews the relationships of BUC with PD-1/PD-L1 and CTLA-4 pathways,as demonstrated in clinical trials.In particular,the authors elucidate the clinical studies on the application of immune checkpoint inhibitors in different BUC stages and their optimal combining strategies,with an attempt to improve the clinical use of immune inhibitors for BUC treatment.


Subject(s)
Apoptosis , B7-H1 Antigen , CTLA-4 Antigen , Immunotherapy , Programmed Cell Death 1 Receptor , Signal Transduction
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