Sintilimab plus docetaxel as second-line therapy of advanced non-small cell lung cancer without targetable mutations: a phase II efficacy and biomarker study

Highlights • Survival outcomes of patients with NSCLC without targetable mutations remain depressing. • Sintilimab plus docetaxel as second-line therapy improves progression-free survival outcomes. • Sintilimab plus docetaxel is safe and well-tolerated. • Patients detected with high PD-L1 expression...

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Main Authors: Yongchang Zhang, Lianxi Song, Liang Zeng, Yi Xiong, Li Liu, Chunhua Zhou, Haiyan Yang, Zhan Wang, Qing Xia, Wenjuan Jiang, Qinqin Xu, Nong Yang
Format: Article
Language:English
Published: BMC 2022-09-01
Series:BMC Cancer
Subjects:
Online Access:https://doi.org/10.1186/s12885-022-10045-0
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author Yongchang Zhang
Lianxi Song
Liang Zeng
Yi Xiong
Li Liu
Chunhua Zhou
Haiyan Yang
Zhan Wang
Qing Xia
Wenjuan Jiang
Qinqin Xu
Nong Yang
author_facet Yongchang Zhang
Lianxi Song
Liang Zeng
Yi Xiong
Li Liu
Chunhua Zhou
Haiyan Yang
Zhan Wang
Qing Xia
Wenjuan Jiang
Qinqin Xu
Nong Yang
author_sort Yongchang Zhang
collection DOAJ
description Highlights • Survival outcomes of patients with NSCLC without targetable mutations remain depressing. • Sintilimab plus docetaxel as second-line therapy improves progression-free survival outcomes. • Sintilimab plus docetaxel is safe and well-tolerated. • Patients detected with high PD-L1 expression in circulating tumor cells (≥32.5%, median level in 30 patients) achieved significantly higher ORR, PFS and OS. • Patients detected with PD-L1 < 1% and CD8 ≥ 1% expression from their baseline tissue samples had significantly higher ORR (p = 0.026).
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spelling doaj.art-d76394190b1d4ef0bd44e66f043efd2c2022-12-22T04:24:50ZengBMCBMC Cancer1471-24072022-09-0122111310.1186/s12885-022-10045-0Sintilimab plus docetaxel as second-line therapy of advanced non-small cell lung cancer without targetable mutations: a phase II efficacy and biomarker studyYongchang Zhang0Lianxi Song1Liang Zeng2Yi Xiong3Li Liu4Chunhua Zhou5Haiyan Yang6Zhan Wang7Qing Xia8Wenjuan Jiang9Qinqin Xu10Nong Yang11Department of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South UniversityDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South UniversityDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South UniversityDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South UniversityDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South UniversityDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South UniversityDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South UniversityDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South UniversityState Key Laboratory for Oncogenes and Related Genes, Shanghai Cancer Institute, Renji Hospital, Department of Oncology, Shanghai Jiao Tong University School of MedicineDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South UniversityDepartment of Medical Oncology, Qinghai Provincial People’s HospitalDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South UniversityHighlights • Survival outcomes of patients with NSCLC without targetable mutations remain depressing. • Sintilimab plus docetaxel as second-line therapy improves progression-free survival outcomes. • Sintilimab plus docetaxel is safe and well-tolerated. • Patients detected with high PD-L1 expression in circulating tumor cells (≥32.5%, median level in 30 patients) achieved significantly higher ORR, PFS and OS. • Patients detected with PD-L1 < 1% and CD8 ≥ 1% expression from their baseline tissue samples had significantly higher ORR (p = 0.026).https://doi.org/10.1186/s12885-022-10045-0Sintilimab plus docetaxelNSCLCCTC-PD-L1Multiplex immunofluorescence
spellingShingle Yongchang Zhang
Lianxi Song
Liang Zeng
Yi Xiong
Li Liu
Chunhua Zhou
Haiyan Yang
Zhan Wang
Qing Xia
Wenjuan Jiang
Qinqin Xu
Nong Yang
Sintilimab plus docetaxel as second-line therapy of advanced non-small cell lung cancer without targetable mutations: a phase II efficacy and biomarker study
BMC Cancer
Sintilimab plus docetaxel
NSCLC
CTC-PD-L1
Multiplex immunofluorescence
title Sintilimab plus docetaxel as second-line therapy of advanced non-small cell lung cancer without targetable mutations: a phase II efficacy and biomarker study
title_full Sintilimab plus docetaxel as second-line therapy of advanced non-small cell lung cancer without targetable mutations: a phase II efficacy and biomarker study
title_fullStr Sintilimab plus docetaxel as second-line therapy of advanced non-small cell lung cancer without targetable mutations: a phase II efficacy and biomarker study
title_full_unstemmed Sintilimab plus docetaxel as second-line therapy of advanced non-small cell lung cancer without targetable mutations: a phase II efficacy and biomarker study
title_short Sintilimab plus docetaxel as second-line therapy of advanced non-small cell lung cancer without targetable mutations: a phase II efficacy and biomarker study
title_sort sintilimab plus docetaxel as second line therapy of advanced non small cell lung cancer without targetable mutations a phase ii efficacy and biomarker study
topic Sintilimab plus docetaxel
NSCLC
CTC-PD-L1
Multiplex immunofluorescence
url https://doi.org/10.1186/s12885-022-10045-0
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