Evidence map›Paper›PMID 38212845›Full record

ArticleBreast cancer research : BCR2024

Prognostic value of baseline neutrophil/lymphocyte ratio in HER2-positive metastatic breast cancer: exploratory analysis of data from the CLEOPATRA trial.

Nianhua Ding, Jian Pang, Xuan Liu, Xiongbin He, Wei Zhou, Haiqing Xie, Jianqi Feng, Guo Wang, Jie Tang, Jing Cao and 4 more

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.1field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 7 institutions in 1 country.

Nianhua Ding *Department of Clinical Laboratory, The Affiliated Changsha Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Jian Pang *Department of General Surgery, The Second Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Xuan LiuDepartment of General Surgery, The First People's Hospital of Xiangtan, Xiangtan, People's Republic of China.
Xiongbin HeDepartment of Breast and Thyroid Surgery, The First People's Hospital of Chenzhou, Chenzhou, People's Republic of China.
Wei ZhouDepartment of Breast Surgery, The Affiliated Zhuzhou Hospital of Xiangya School of Medicine, Zhuzhou, People's Republic of China.
Haiqing XieDepartment of Breast and Thyroid Surgery, The Third People's Hospital of Chenzhou, Chenzhou, People's Republic of China.
Jianqi FengDepartment of Breast and Thyroid Surgery, The First People's Hospital of Huaihua, Huaihua, People's Republic of China.
Guo WangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Jie TangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Jing CaoDepartment of Breast SurgeryXiangya Hospital, Central South University, Changsha, People's Republic of China.
Liying HeDepartment of Clinical Laboratory, The Affiliated Changsha Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Yingjian HeKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Breast Center, Peking University Cancer Hospital and Institute, Beijing, People's Republic of China.
Shouman WangDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Zhi XiaoDepartment of Breast Surgery, General Surgery, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008, Hunan, People's Republic of China. zhixiao@csu.edu.cn.
Central South University · CNXiangya Hospital Central South University · CNChenzhou First People's Hospital · CNHuaian First People’s Hospital · CNPeking University · CNXiang Yang No.1 People's Hospital · CNZhuzhou Central Hospital · CN

Funding

Natural Science Foundation of Changsha City KQ2007058Natural Science Foundation of Hunan Province 2021JJ31094Natural Science Foundation of Hunan Province 2021JJ31099Natural Science Foundation of Hunan Province S2019JJKWLH0198
6 · The paper itself

Abstract

purposeThis study aimed to evaluate the prognostic role of the baseline neutrophil/lymphocyte ratio (NLR) in HER2-positive metastatic breast cancer (MBC) patients treated with trastuzumab/pertuzumab. EXPERIMENTAL

designData from 780 patients from the CLEOPATRA trial and 248 local patients were collected. Patients were divided into the low and high NLR subgroups by the NLR cutoff value. Propensity score matching (PSM) and inverse probability of treatment weighting (IPTW) methods were used to control bias. Associations between the NLR and progression-free survival (PFS) and overall survival (OS) were analyzed.

resultsThe baseline characteristics of the subgroups were well balanced after PSM and IPTW. A low baseline NLR was associated with better PFS and OS in the trastuzumab and docetaxel (TH) group in the unadjusted, PSM and IPTW models. After IPTW, a low NLR, versus a high NLR, was associated with improved PFS (HR 1.35, 95% CI 1.07-1.70, P = 0.012) and OS (HR 1.47, 95% CI 1.12-1.94, P = 0.006) in the TH group. In patients undergoing treatment with trastuzumab and pertuzumab and docetaxel (THP), a low baseline NLR was also correlated with better PFS but not OS across the three models. After IPTW, a low NLR was associated with better PFS (HR 1.52, 95% CI 1.20-1.93, P = 0.001) than a high NLR in the THP group. Multivariate analyses showed that a low baseline NLR was a predictor for PFS and OS in the TH group and for PFS in the THP group in all three models. In the real-world setting, a low baseline NLR was a predictor of better PFS among patients treated with docetaxel plus trastuzumab without or with pertuzumab in the multivariate model (P = 0.015 and 0.008, respectively).

conclusionsA low baseline NLR is associated with better survival outcomes among HER2-positive MBC patients receiving docetaxel plus trastuzumab/pertuzumab as first-line therapy.

Indexed as

Breast NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsDocetaxelErb-b2 Receptor Tyrosine KinasesFemaleHumansLymphocytesNeutrophilsPrognosisTrastuzumabDocetaxelErb-b2 Receptor Tyrosine KinasesTrastuzumabHER2-positiveMetastatic breast cancerNeutrophil/lymphocyte ratioPrognostic valueTrastuzumab/pertuzumab

Identifiers

PMID38212845
PMCPMC10785455
OpenAlexW4390753601

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.