Toripalimab plus nab-paclitaxel in metastatic or recurrent triple-negative breast cancer: a randomized phase 3 trial

The combination of immune-checkpoint blockade with chemotherapy for the first-line treatment of advanced triple-negative breast cancer (TNBC) has generated mixed results. TORCHLIGHT is a randomized, double-blinded phase 3 trial evaluating the efficacy and safety of first-line toripalimab and nab-pac...

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Published inNature medicine Vol. 30; no. 1; pp. 249 - 256
Main Authors Jiang, Zefei, Ouyang, Quchang, Sun, Tao, Zhang, Qingyuan, Teng, Yuee, Cui, Jiuwei, Wang, Haibo, Yin, Yongmei, Wang, Xiaojia, Zhou, Xin, Wang, Yongsheng, Sun, Gang, Wang, Jingfen, Zhang, Lili, Yang, Jin, Qian, Jun, Yan, Min, Liu, Xinlan, Yi, Tienan, Cheng, Ying, Li, Man, Zang, Aimin, Wang, Shusen, Wang, Chuan, Wu, Xinhong, Cheng, Jing, Li, Hui, Lin, Ying, Geng, Cuizhi, Gu, Kangsheng, Xie, Chunwei, Xiong, Huihua, Wu, Xiaohong, Yang, Junlan, Li, Qingshan, Chen, Yiding, Li, Fanfan, Zhang, Anqin, Zhang, Yongqiang, Wu, Yudong, Nie, Jianyun, Liu, Qiang, Wang, Kun, Mo, Xueli, Chen, Lilin, Pan, Yueyin, Fu, Peifen, Zhang, Helong, Pang, Danmei, Sheng, Yuan, Han, Yunwei, Wang, Hongxia, Cang, Shundong, Luo, Xianming, Yu, Wenbo, Deng, Rong, Yang, Chaoqiang, Keegan, Patricia
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Published New York Nature Publishing Group US 2024
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Abstract The combination of immune-checkpoint blockade with chemotherapy for the first-line treatment of advanced triple-negative breast cancer (TNBC) has generated mixed results. TORCHLIGHT is a randomized, double-blinded phase 3 trial evaluating the efficacy and safety of first-line toripalimab and nab-paclitaxel (nab-P) ( n  = 353; experimental arm) versus placebo and nab-P ( n  = 178; control arm) for the treatment of women with metastatic or recurrent TNBC. The primary end point was progression-free survival (PFS) assessed by a blinded independent central review in the PD-L1-positive and intention-to-treat populations. The secondary end points included overall survival and safety. Overall, 200 and 100 patients, in the toripalimab and placebo arm respectively had PD-L1-positive TNBC. At the prespecified interim analysis, a statistically significant improvement in PFS assessed by a blinded independent central review was demonstrated in the experimental arm in the PD-L1-positive population (median PFS 8.4 versus 5.6 months; hazard ratio (HR) = 0.65, 95% confidence interval (CI) 0.470–0.906, P  = 0.0102). The median overall survival was 32.8 versus 19.5 months (HR = 0.62, 95% CI 0.414–0.914, P  = 0.0148). Similar incidences of treatment-emergent adverse events (AEs) (99.2% versus 98.9%), grade ≥3 treatment-emergent AEs (56.4% versus 54.3%) and fatal AEs (0.6% versus 3.4%) occurred in the experimental and control arms. The addition of toripalimab to nab-P provided a significant improvement in PFS for PD-L1-positive patients with metastatic or recurrent TNBC with an acceptable safety profile. ClinicalTrial.gov identifier NCT03777579 . In this prespecified analysis of the ongoing TORCHLIGHT phase 3 trial, first-line treatment with toripalimab and nab-paclitaxel in patients with advanced triple-negative breast cancer led to significantly longer progression-free survival in the PD-L1-positive population compared to nab-paclitaxel alone.
AbstractList The combination of immune-checkpoint blockade with chemotherapy for the first-line treatment of advanced triple-negative breast cancer (TNBC) has generated mixed results. TORCHLIGHT is a randomized, double-blinded phase 3 trial evaluating the efficacy and safety of first-line toripalimab and nab-paclitaxel (nab-P) (n = 353; experimental arm) versus placebo and nab-P (n = 178; control arm) for the treatment of women with metastatic or recurrent TNBC. The primary end point was progression-free survival (PFS) assessed by a blinded independent central review in the PD-L1-positive and intention-to-treat populations. The secondary end points included overall survival and safety. Overall, 200 and 100 patients, in the toripalimab and placebo arm respectively had PD-L1-positive TNBC. At the prespecified interim analysis, a statistically significant improvement in PFS assessed by a blinded independent central review was demonstrated in the experimental arm in the PD-L1-positive population (median PFS 8.4 versus 5.6 months; hazard ratio (HR) = 0.65, 95% confidence interval (CI) 0.470-0.906, P = 0.0102). The median overall survival was 32.8 versus 19.5 months (HR = 0.62, 95% CI 0.414-0.914, P = 0.0148). Similar incidences of treatment-emergent adverse events (AEs) (99.2% versus 98.9%), grade ≥3 treatment-emergent AEs (56.4% versus 54.3%) and fatal AEs (0.6% versus 3.4%) occurred in the experimental and control arms. The addition of toripalimab to nab-P provided a significant improvement in PFS for PD-L1-positive patients with metastatic or recurrent TNBC with an acceptable safety profile. ClinicalTrial.gov identifier NCT03777579 .The combination of immune-checkpoint blockade with chemotherapy for the first-line treatment of advanced triple-negative breast cancer (TNBC) has generated mixed results. TORCHLIGHT is a randomized, double-blinded phase 3 trial evaluating the efficacy and safety of first-line toripalimab and nab-paclitaxel (nab-P) (n = 353; experimental arm) versus placebo and nab-P (n = 178; control arm) for the treatment of women with metastatic or recurrent TNBC. The primary end point was progression-free survival (PFS) assessed by a blinded independent central review in the PD-L1-positive and intention-to-treat populations. The secondary end points included overall survival and safety. Overall, 200 and 100 patients, in the toripalimab and placebo arm respectively had PD-L1-positive TNBC. At the prespecified interim analysis, a statistically significant improvement in PFS assessed by a blinded independent central review was demonstrated in the experimental arm in the PD-L1-positive population (median PFS 8.4 versus 5.6 months; hazard ratio (HR) = 0.65, 95% confidence interval (CI) 0.470-0.906, P = 0.0102). The median overall survival was 32.8 versus 19.5 months (HR = 0.62, 95% CI 0.414-0.914, P = 0.0148). Similar incidences of treatment-emergent adverse events (AEs) (99.2% versus 98.9%), grade ≥3 treatment-emergent AEs (56.4% versus 54.3%) and fatal AEs (0.6% versus 3.4%) occurred in the experimental and control arms. The addition of toripalimab to nab-P provided a significant improvement in PFS for PD-L1-positive patients with metastatic or recurrent TNBC with an acceptable safety profile. ClinicalTrial.gov identifier NCT03777579 .
The combination of immune-checkpoint blockade with chemotherapy for the first-line treatment of advanced triple-negative breast cancer (TNBC) has generated mixed results. TORCHLIGHT is a randomized, double-blinded phase 3 trial evaluating the efficacy and safety of first-line toripalimab and nab-paclitaxel (nab-P) ( n  = 353; experimental arm) versus placebo and nab-P ( n  = 178; control arm) for the treatment of women with metastatic or recurrent TNBC. The primary end point was progression-free survival (PFS) assessed by a blinded independent central review in the PD-L1-positive and intention-to-treat populations. The secondary end points included overall survival and safety. Overall, 200 and 100 patients, in the toripalimab and placebo arm respectively had PD-L1-positive TNBC. At the prespecified interim analysis, a statistically significant improvement in PFS assessed by a blinded independent central review was demonstrated in the experimental arm in the PD-L1-positive population (median PFS 8.4 versus 5.6 months; hazard ratio (HR) = 0.65, 95% confidence interval (CI) 0.470–0.906, P  = 0.0102). The median overall survival was 32.8 versus 19.5 months (HR = 0.62, 95% CI 0.414–0.914, P  = 0.0148). Similar incidences of treatment-emergent adverse events (AEs) (99.2% versus 98.9%), grade ≥3 treatment-emergent AEs (56.4% versus 54.3%) and fatal AEs (0.6% versus 3.4%) occurred in the experimental and control arms. The addition of toripalimab to nab-P provided a significant improvement in PFS for PD-L1-positive patients with metastatic or recurrent TNBC with an acceptable safety profile. ClinicalTrial.gov identifier NCT03777579 . In this prespecified analysis of the ongoing TORCHLIGHT phase 3 trial, first-line treatment with toripalimab and nab-paclitaxel in patients with advanced triple-negative breast cancer led to significantly longer progression-free survival in the PD-L1-positive population compared to nab-paclitaxel alone.
The combination of immune-checkpoint blockade with chemotherapy for the first-line treatment of advanced triple-negative breast cancer (TNBC) has generated mixed results. TORCHLIGHT is a randomized, double-blinded phase 3 trial evaluating the efficacy and safety of first-line toripalimab and nab-paclitaxel (nab-P) (n = 353; experimental arm) versus placebo and nab-P (n = 178; control arm) for the treatment of women with metastatic or recurrent TNBC. The primary end point was progression-free survival (PFS) assessed by a blinded independent central review in the PD-L1-positive and intention-to-treat populations. The secondary end points included overall survival and safety. Overall, 200 and 100 patients, in the toripalimab and placebo arm respectively had PD-L1-positive TNBC. At the prespecified interim analysis, a statistically significant improvement in PFS assessed by a blinded independent central review was demonstrated in the experimental arm in the PD-L1-positive population (median PFS 8.4 versus 5.6 months; hazard ratio (HR) = 0.65, 95% confidence interval (CI) 0.470–0.906, P = 0.0102). The median overall survival was 32.8 versus 19.5 months (HR = 0.62, 95% CI 0.414–0.914, P = 0.0148). Similar incidences of treatment-emergent adverse events (AEs) (99.2% versus 98.9%), grade ≥3 treatment-emergent AEs (56.4% versus 54.3%) and fatal AEs (0.6% versus 3.4%) occurred in the experimental and control arms. The addition of toripalimab to nab-P provided a significant improvement in PFS for PD-L1-positive patients with metastatic or recurrent TNBC with an acceptable safety profile. ClinicalTrial.gov identifier NCT03777579.In this prespecified analysis of the ongoing TORCHLIGHT phase 3 trial, first-line treatment with toripalimab and nab-paclitaxel in patients with advanced triple-negative breast cancer led to significantly longer progression-free survival in the PD-L1-positive population compared to nab-paclitaxel alone.
The combination of immune-checkpoint blockade with chemotherapy for the first-line treatment of advanced triple-negative breast cancer (TNBC) has generated mixed results. TORCHLIGHT is a randomized, double-blinded phase 3 trial evaluating the efficacy and safety of first-line toripalimab and nab-paclitaxel (nab-P) (n = 353; experimental arm) versus placebo and nab-P (n = 178; control arm) for the treatment of women with metastatic or recurrent TNBC. The primary end point was progression-free survival (PFS) assessed by a blinded independent central review in the PD-L1-positive and intention-to-treat populations. The secondary end points included overall survival and safety. Overall, 200 and 100 patients, in the toripalimab and placebo arm respectively had PD-L1-positive TNBC. At the prespecified interim analysis, a statistically significant improvement in PFS assessed by a blinded independent central review was demonstrated in the experimental arm in the PD-L1-positive population (median PFS 8.4 versus 5.6 months; hazard ratio (HR) = 0.65, 95% confidence interval (CI) 0.470-0.906, P = 0.0102). The median overall survival was 32.8 versus 19.5 months (HR = 0.62, 95% CI 0.414-0.914, P = 0.0148). Similar incidences of treatment-emergent adverse events (AEs) (99.2% versus 98.9%), grade ≥3 treatment-emergent AEs (56.4% versus 54.3%) and fatal AEs (0.6% versus 3.4%) occurred in the experimental and control arms. The addition of toripalimab to nab-P provided a significant improvement in PFS for PD-L1-positive patients with metastatic or recurrent TNBC with an acceptable safety profile. ClinicalTrial.gov identifier NCT03777579 .
Author Deng, Rong
Wang, Xiaojia
Liu, Xinlan
Wu, Yudong
Li, Fanfan
Sheng, Yuan
Yu, Wenbo
Sun, Tao
Wang, Jingfen
Wu, Xinhong
Chen, Yiding
Cui, Jiuwei
Yan, Min
Zhang, Anqin
Zhang, Lili
Lin, Ying
Ouyang, Quchang
Wang, Haibo
Cang, Shundong
Mo, Xueli
Teng, Yuee
Geng, Cuizhi
Luo, Xianming
Pan, Yueyin
Yin, Yongmei
Zhou, Xin
Liu, Qiang
Yi, Tienan
Wang, Kun
Keegan, Patricia
Jiang, Zefei
Yang, Chaoqiang
Gu, Kangsheng
Cheng, Ying
Wang, Hongxia
Qian, Jun
Cheng, Jing
Wu, Xiaohong
Li, Man
Xie, Chunwei
Yang, Junlan
Zhang, Yongqiang
Chen, Lilin
Zhang, Helong
Sun, Gang
Zhang, Qingyuan
Wang, Chuan
Han, Yunwei
Xiong, Huihua
Wang, Yongsheng
Fu, Peifen
Li, Hui
Pang, Danmei
Yang, Jin
Zang, Aimin
Nie, Jianyun
Wang, Shusen
Li, Qingshan
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crossref_primary_10_1016_j_annonc_2024_04_001
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2024. The Author(s), under exclusive licence to Springer Nature America, Inc.
Copyright_xml – notice: The Author(s), under exclusive licence to Springer Nature America, Inc. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
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References Chang (CR16) 2019; 37
O’Meara, Tolaney (CR3) 2021; 12
Ramos-Casals (CR15) 2020; 6
Tang (CR8) 2020; 26
Schmid (CR5) 2018; 379
Sung (CR1) 2021; 71
Bian (CR14) 2019; 7
Liu (CR13) 2019; 11
Wang (CR17) 2023; 41
CR11
Cortes (CR7) 2022; 387
Sheng (CR10) 2020; 38
Waks, Winer (CR2) 2019; 321
Mai (CR12) 2021; 27
Miles (CR6) 2021; 32
Goodman (CR4) 2017; 16
Wang (CR9) 2021; 39
B Tang (2677_CR8) 2020; 26
2677_CR11
FH Wang (2677_CR9) 2021; 39
E Chang (2677_CR16) 2019; 37
AG Waks (2677_CR2) 2019; 321
L Bian (2677_CR14) 2019; 7
Z Wang (2677_CR17) 2023; 41
H Sung (2677_CR1) 2021; 71
X Sheng (2677_CR10) 2020; 38
D Miles (2677_CR6) 2021; 32
H-Q Mai (2677_CR12) 2021; 27
TA O’Meara (2677_CR3) 2021; 12
H Liu (2677_CR13) 2019; 11
M Ramos-Casals (2677_CR15) 2020; 6
J Cortes (2677_CR7) 2022; 387
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Snippet The combination of immune-checkpoint blockade with chemotherapy for the first-line treatment of advanced triple-negative breast cancer (TNBC) has generated...
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SubjectTerms 692/308/2779/777
692/699/67/1347
Biomedical and Life Sciences
Biomedicine
Breast cancer
Cancer Research
Chemotherapy
Confidence intervals
Immune checkpoint inhibitors
Infectious Diseases
Metabolic Diseases
Metastases
Metastasis
Molecular Medicine
Neurosciences
Paclitaxel
PD-L1 protein
Placebos
Safety
Statistical analysis
Survival
Title Toripalimab plus nab-paclitaxel in metastatic or recurrent triple-negative breast cancer: a randomized phase 3 trial
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