Yanqiu Zhao

ORCID: 0000-0003-0161-6184
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About
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Research Areas
  • Lung Cancer Treatments and Mutations
  • Lung Cancer Research Studies
  • Colorectal Cancer Treatments and Studies
  • Cancer Immunotherapy and Biomarkers
  • Cancer therapeutics and mechanisms
  • Lung Cancer Diagnosis and Treatment
  • Cancer Genomics and Diagnostics
  • Gastric Cancer Management and Outcomes
  • Peptidase Inhibition and Analysis
  • Neuroendocrine Tumor Research Advances
  • HER2/EGFR in Cancer Research
  • Radiomics and Machine Learning in Medical Imaging
  • Brain Metastases and Treatment
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • MicroRNA in disease regulation
  • Pancreatic and Hepatic Oncology Research
  • Nanoparticle-Based Drug Delivery
  • Monoclonal and Polyclonal Antibodies Research
  • Genetic factors in colorectal cancer
  • Thyroid Cancer Diagnosis and Treatment
  • RNA modifications and cancer
  • Cancer Research and Treatments
  • HIV/AIDS Research and Interventions
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Hedgehog Signaling Pathway Studies

Henan Cancer Hospital
2016-2025

Zhengzhou University
2016-2025

Kunming Medical University
2024-2025

Peking University
2024-2025

First Affiliated Hospital of Harbin Medical University
2024-2025

Cancer Hospital of Huanxing Chaoyang District Beijing
2025

Harbin Medical University
2025

Sichuan International Studies University
2022-2024

Ludong University
2024

Peking University Cancer Hospital
2024

Luis Paz‐Ares Mikhail Dvorkin Yuanbin Chen Niels Reinmuth Katsuyuki Hotta and 95 more Dmytro Trukhin Galina Statsenko Maximilian J. Hochmair Mustafa Özgüroğlu Jun Ho Ji Олександр Войтко Artem Poltoratskiy Santiago Ponce Francesco Verderame Libor Havel Igor Bondarenko Andrzej Każarnowicz György Losonczy Nikolay Conev J. Armstrong Natalie Byrne Norah J. Shire Haiyi Jiang Jonathan W. Goldman Emilio Batagelj Ignacio Casarini Anea Viviana Pastor S. Sena Juan José Zarbá Otto C. Burghuber Sylvia Hartl Maximilian J. Hochmair Bernd Lamprecht Michael Studnicka Luís Alberto Schlittler Fabrício Augusto Martinelli de Oliveira Aknar Calabrich Gustavo Girotto Peo Dos Reis Carlos Fausto Nino Gorini Peo Rafael Martins De Marchi Clarissa Baldotto Cláudia Vaz de Melo Sette Mauro Zukin Nikolay Conev Assen Dudov Rumyana Ilieva Krassimir Koynov Rositsa Krasteva Ivan Tonev Spartak Valev Violetka Venkova Minghong Bi Chengshui Chen Yuan Chen Zhendong Chen Jian Fang Jifeng Feng Zhigang Han Jie Hu Yi Hu Xing Li Zongan Liang Lin Zhong Rui Ma Shenglin Ma Kejun Nan Yongqian Shu Kai Wang Mengzhao Wang Gang Wu Nong Yang Zhixiong Yang Helong Zhang Wei Zhang Jun Zhao Yanqiu Zhao Caicun Zhou Jianying Zhou Xiangdong Zhou Libor Havel Vı́tězslav Kolek Leona Koubková Jaromı́r Roubec Jana Skřičková Milada Zemanová C. Chouaïd Werner Hilgers H. Léna Denis Moro‐Sibilot G. Robinet Pierre-Jean Souquet Jürgen Alt Helge Bischoff Christian Grohé Eckart Laack Susanne Lang Jens Panse Niels Reinmuth Christian Schulz

10.1016/s0140-6736(19)32222-6 article EN The Lancet 2019-10-04

IntroductionSintilimab, an anti–programmed death 1 antibody, plus pemetrexed and platinum had revealed promising efficacy for nonsquamous NSCLC in a phase 1b study. We conducted randomized, double-blind, 3 study to compare the safety of sintilimab with placebo, both combination such chemotherapy (ClinicalTrials.gov: NCT03607539).MethodsA total 397 patients previously untreated, locally advanced or metastatic without sensitizing EGFR anaplastic lymphoma kinase genomic aberration were...

10.1016/j.jtho.2020.07.014 article EN cc-by-nc-nd Journal of Thoracic Oncology 2020-08-08

Importance Programmed cell death ligand 1 inhibitors combined with chemotherapy has changed the approach to first-line treatment in patients extensive-stage small lung cancer (SCLC). It remained unknown whether adding a programmed (PD-1) inhibitor provided similar or better benefits SCLC, which would add evidence on efficacy of checkpoint SCLC. Objective To evaluate and adverse event profile PD-1 serplulimab plus compared placebo as Design, Setting, Participants This international,...

10.1001/jama.2022.16464 article EN JAMA 2022-09-27

Inhibiting vascular endothelial growth factor (VEGF) function can improve the efficacy of immunotherapy by modulating tumor immune microenvironment. AK112 is first-in-class humanized IgG1 bispecific antibody targeting programmed death-1 (PD-1) and VEGF. This study aimed to evaluate safety combined with chemotherapy in patients advanced non-small cell lung cancer (NSCLC).This open-label, multicenter, phase II clinical trial was conducted 11 hospitals China. Eligible participants were adults...

10.1016/j.eclinm.2023.102106 article EN cc-by-nc-nd EClinicalMedicine 2023-08-01

Osimertinib has shown promising activity in patients with leptomeningeal metastases (LMs) of EGFR-positive NSCLC at 160 mg once daily (qd) (BLOOM; NCT02228369). We report LM osimertinib (80 qd) a retrospective analysis studies across the AURA program (AURA extension, AURA2, AURA17, and AURA3).Patients EGFR T790M-positive advanced progression after previous EGFR-tyrosine kinase inhibitor therapy received qd). Patients central nervous system (CNS) (including LMs) were eligible if lesions...

10.1016/j.jtho.2019.12.113 article EN cc-by-nc-nd Journal of Thoracic Oncology 2019-12-28

Abstract Exosomes are small endogenous membrane vesicles that can mediate cell communication by transferring genetic materials. Based on that, exosomes have always been discussed as a cargo carrier for microRNA (miRNA) transportation. Accumulating data reported the inhibitory effects of microRNA-193a (miR-193a) non-small lung cancer (NSCLC) progression. However, mechanisms miR-193a delivery to cells and in not explored clearly NSCLC. Given this work aims decode exosomal cisplatin (DDP)...

10.1038/s41419-020-02962-4 article EN cc-by Cell Death and Disease 2020-09-25

This multicenter phase-II trial aimed to investigate the efficacy, safety, and predictive biomarkers of toripalimab plus chemotherapy as second-line treatment in patients with EGFR-mutant-advanced NSCLC. Patients who failed from first-line EGFR-TKIs did not harbor T790M mutation were enrolled. Toripalimab carboplatin pemetrexed administrated every three weeks for up six cycles, followed by maintenance pemetrexed. The primary endpoint was objective-response rate (ORR). Integrated biomarker...

10.1038/s41392-021-00751-9 article EN cc-by Signal Transduction and Targeted Therapy 2021-10-15

Epidermal growth factor receptor exon 20 insertion mutations (EGFRexon20ins) are detected in approximately 2% of patients with non-small cell lung cancer (NSCLC). Due to a lack effective therapy, the prognosis these is typically poor. Sunvozertinib (DZD9008) was designed as an oral, potent, irreversible, and selective EGFR tyrosine kinase inhibitor, showing activity against EGFRexon20ins other mutations. In both lines xenograft models, sunvozertinib shows potent antitumor activity. two...

10.1158/2159-8290.cd-21-1615 article EN cc-by-nc-nd Cancer Discovery 2022-04-11

Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) have been widely used for human non-small-cell lung cancer (NSCLC) treatment. However, acquired resistance to EGFR-TKIs is the major barrier of treatment success, and new mechanism remains be elucidated. In this study, we found that elevated NADPH oxidase 4 (NOX4) expression was associated with resistance. Gefitinib first-generation FDA-approved EGFR-TKI, osimertinib third-generation EGFR-TKI. We demonstrated NOX4...

10.1016/j.drup.2023.100987 article EN cc-by-nc-nd Drug Resistance Updates 2023-06-22

This open-label, phase 3 trial (ALTA-3; NCT03596866) compared efficacy and safety of brigatinib versus alectinib for ALK+ NSCLC after disease progression on crizotinib.Patients with advanced that progressed crizotinib were randomized 1:1 to 180 mg once daily (7-d lead-in, 90 mg) or 600 twice daily, aiming test superiority. The primary end point was blinded independent review committee-assessed progression-free survival (PFS). Interim analysis futility planned at approximately 70% 164...

10.1016/j.jtho.2023.08.010 article EN cc-by Journal of Thoracic Oncology 2023-08-12

We conducted a proof-of-concept, phase 2 trial to assess neoadjuvant SHR-1701 with or without chemotherapy, followed by surgery radiotherapy, and then consolidation in unresectable stage III non-small-cell lung cancer (NSCLC). In the primary cohort of patients receiving combination therapy (n = 97), both endpoints were met, post-induction objective response rate 58% (95% confidence interval [CI] 47–68) an 18-month event-free survival (EFS) 56.6% CI 45.2–66.5). Overall, 27 (25%) underwent...

10.1016/j.ccell.2024.05.024 article EN cc-by-nc-nd Cancer Cell 2024-06-20

Abstract Background Treatment options for Chinese patients with locally advanced or metastatic squamous‐cell non‐small‐cell lung cancer (sqNSCLC) after failure of first‐line chemotherapy are limited. This study (ORIENT‐3) aimed to evaluate the efficacy and safety sintilimab versus docetaxel as second‐line treatment in sqNSCLC. Methods ORIENT‐3 was an open‐label, multicenter, randomized controlled phase 3 trial that recruited stage IIIB/IIIC/IV sqNSCLC platinum‐based chemotherapy. Patients...

10.1002/cac2.12385 article EN cc-by-nc-nd Cancer Communications 2022-11-06

9002 Background: Sunvozertinib(DZD9008) is a rationally designed selective, irreversible EGFR exon20 insertion (exon20ins) inhibitor with wild-type selectivity. Here we reported the results of WU-KONG6, first pivotal study sunvozertinib in previously treated NSCLC patients exon20ins. Methods: WU-KONG6 (NCT05712902 and CTR20211009) phase II, multi-center exon20ins, whose diseases had progressed on or were after platinum-based chemotherapy. Tumor tissue exon20ins status was tested by local...

10.1200/jco.2023.41.16_suppl.9002 article EN Journal of Clinical Oncology 2023-06-01

468214 Background: KRAS G12C mutation occurs in approximately 4% of non-small cell lung cancers (NSCLC) China. Glecirasib (Jacobio, Beijing, PRC) is a potent and highly selective covalent oral inhibitor G12C. Methods: This phase 2 single-arm study (NCT05009329) glecirasib was conducted China at 43 sites, enrolling participants with locally advanced or metastatic mutated NSCLC. Subjects must have received prior platinum-based therapy an immune checkpoint (ICI) as well appropriate targeted...

10.1200/jco.2024.42.36_suppl.468214 article EN Journal of Clinical Oncology 2024-04-30
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