Evidence map›Paper›PMID 32108439›Full record

ArticleCancer medicine2020

Real-world data of lapatinib and treatment after lapatinib in patients with previously treated HER2-positive metastatic breast cancer: A multicenter, retrospective study.

Yizhao Xie, Rui Ge, Die Sang, Ting Luo, Wei Li, Xuening Ji, Peng Yuan, Biyun Wang

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Cancer medicine, 2020. 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
0.2field-weighted citation impact, top 50% 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

8 authors at 7 institutions in 1 country.

Yizhao XieDepartment of Medical Oncology, Department of Oncology, Fudan University Shanghai Cancer Center, Shanghai Medical College, Fudan University, Shanghai, China.
Rui GeHuadong Hospital Affiliated to Fudan University, Shanghai, China.
Die SangDepartment of Oncology, San Huan Cancer Hospital, Beijing, China.
Ting LuoDepartment of Head, Neck and Mammary Gland Oncology, Cancer Center, West China Hospital, Sichuan University, Sichuan, China.
Wei LiDepartment of Medical Oncology, Jiangsu Province Hospital, Nanjing, China.
Xuening JiDepartment of Oncology, Affiliated Zhongshan Hospital of Dalian University, Dalian, China.
Peng YuanNational Cancer Center, Tumor Hospital of the Chinese Academy of Medical Sciences, Beijing, China.
Biyun WangDepartment of Medical Oncology, Department of Oncology, Fudan University Shanghai Cancer Center, Shanghai Medical College, Fudan University, Shanghai, China.ORCID 0000-0002-7829-1544
Fudan University Shanghai Cancer Center · CNAffiliated Zhongshan Hospital of Dalian University · CNCancer Hospital of Huanxing Chaoyang District Beijing · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNFudan University · CNJiangsu Province Hospital · CNSichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lapatinib is widely used in the later lines treatment of HER2 positive metastatic breast cancer (MBC). EGF104900 study suggested that among patients who experienced progression on prior trastuzumab-containing regimens, lapatinib plus trastuzumab had better effects than trastuzumab alone. However, no evidence was discovered in terms of lapatinib plus capetabine compared with lapatinib plus trastuzumab plus chemotherapy, as well as a treatment after progression on lapatinib. We evaluated the medical records retrospectively of all MBC patients with HER2 positive disease who progressed on prior trastuzumab-containing regimens (advanced setting) and a taxane (any setting) and received lapatinib-based treatment from 2015 to 2018 in five institutions in China. A total of 242 patients were available for analysis. Among them, 164 (68%) patients received lapatinib plus capetabine (LX) and 78 (32%) patients received lapatinib plus trastuzumab and one chemotherapy (HLC). The median progression-free survival (PFS) of the HLC group was significantly superior to the LX group (8.8 months vs 5.0 months, P < .0000001). No significant difference in grade 3 or worse adverse events was observed in two groups (P = .57). A total of 175 patients were available for the analysis of the postlapatinib treatment. Continuation of lapatinib showed superior mPFS results compared to the non-anti-HER2 treatment (4 months vs 2 months, P = .01) and similar results compared to switch to other anti-HER2 treatments (4 months vs 4 months, P = .88). In patients who had progressed on prior trastuzumab-base therapy, HLC provided a new dual-targeting treatment option for the later lines therapy of patients with HER2 positive MBC. Moreover, evidence of cross-line use of lapatinib was provided.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesFemaleFollow-Up StudiesHumansLapatinibMiddle AgedNeoplasm MetastasisPrognosisRetrospective StudiesSurvival RateBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesLapatinibTrastuzumabchemotherapyclinical studyHer2lapatinibmetastatic breast cancer

Identifiers

PMID32108439
PMCPMC7196046
OpenAlexW3007718650

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.