Evidence map›Paper›PMID 37568079›Full record

ArticleBMC cancer2023

First-line induction chemotherapy with high-dose methotrexate versus teniposide in patients with newly diagnosed primary central nervous system lymphoma: a retrospective, multicenter cohort study.

Kaili Zhong, Yanyan Shi, Yuhuan Gao, Huilai Zhang, Mingzhi Zhang, Qiaohua Zhang, Xinan Cen, Mei Xue, Yan Qin, Yu Zhao and 11 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
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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

21 authors at 16 institutions in 1 country.

Kaili Zhong *Department of Lymphoma, Beijing Shijitan Hospital, Capital Medical University, Beijing, China. zhongkaili3443@bjsjth.cn.
Yanyan Shi *Research Center of Clinical Epidemiology, Peking University Third Hospital, Beijing, China.
Yuhuan GaoDepartment of Hematology, Fourth Hospital of Hebei Medical University (Tumor Hospital of Hebei Province), Shijiazhuang, China.
Huilai ZhangDepartment of Lymphoma, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Mingzhi ZhangDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Qiaohua ZhangDepartment of Oncology, Shanxi Academy of Medical Sciences & Shanxi Bethune Hospital, Shanxi Bethune Hospital affiliated to Shanxi Medical University, Taiyuan, China.
Xinan CenDepartment of Hematology, Peking University First Hospital, Beijing, China.
Mei XueDepartment of Hematology, Air Force Medical Center, Beijing, China.
Yan QinDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Yu ZhaoDepartment of Hematology, the General Hospital of PLA, Beijing, China.
Liling ZhangDepartment of Lymphoma, Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Rong LiangDepartment of Hematology, Xijing Hospital, Air Force Military Medical University, Xi'an, China.
Ningju WangDepartment of Medical Oncology, General Hospital of Ningxia Medical University, Yinchuan, China.
Yan XieDepartments of Lymphoma, Key Laboratory of Carcinogenesis and Translational Research, Peking University Cancer Hospital and Institute, Beijing, China.
Yu YangDepartment of Medical Oncology, Fujian Cancer Hospital & Fujian Medical University Cancer Hospital, Fuzhou, China.
Aichun LiuDepartment of Hematology and Lymphoma, Cancer hospital of Harbin Medical University, Haerbin, China.
Huizheng BaoDepartment of Medical Oncology, Jilin Cancer Hospital, Changchun, China.
Jingwen WangDepartment of Hematology, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
Baoping CaoDepartment of Lymphoma, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
Wei ZhangDepartment of Hematology, Peking Union Medical College Hospital, Beijing, China.
Weijing ZhangDepartment of Lymphoma, Beijing Shijitan Hospital, Capital Medical University, Beijing, China. zhangweijing7132@bjsjth.cn.
Beijing Shijitan Hospital · CNPeking University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNAir Force General Hospital PLA · CNBeijing Tongren Hospital · CNFirst Affiliated Hospital of Zhengzhou University · CNFujian Provincial Cancer Hospital · CNHarbin Medical University · CNHebei Medical University · CNJilin Province Tumor Hospital · CNNingxia Medical University · CNShanxi Academy of Medical Sciences · CNThe Military General Hospital of Beijing PLA · CNTianjin Medical University Cancer Institute and Hospital · CNUnion Hospital · CNXijing Hospital · CN

Funding

Capital's Funds for Health Improvement and Research 2018-1-2151Institutional Grant of Beijing Shijitan Hospital, Capital Medical University 2017-c04Research and Cultivation Fund of Capital Medical University PYZ21157
6 · The paper itself

Abstract

backgroundThis study aimed to compare the efficacy and safety of high-dose methotrexate (HD-MTX) versus teniposide (TEN) in patients with newly diagnosed immunocompetent primary central nervous system lymphomas (PCNSLs).

methodsThe study included immunocompetent, adult patients with newly diagnosed PCNSL at 22 centers in China from 2007 to 2016. The patients received HD-MTX or TEN as first-line induction therapy. The objective response rate, progression-free survival, and overall survival were analyzed for each patient cohort.

resultsA total of 96 patients were eligible: 62 received HD-MTX, while 34 received teniposide. The overall response rate was 73.2% and 72.7% in the MTX and the TEN cohorts, respectively (P = 0.627). The median progression-free survival was 28.4 months [95% confidence interval (CI): 13.7-51.2] in the MTX cohort and 24.3 months (95% CI: 16.6-32.1) in the TEN cohort (P = 0.75). The median overall survival was 31 months (95% CI: 26.8-35.2) in the MTX cohort and 32 months (95% CI: 27.6-36.4) in the TEN cohort (P = 0.77). The incidence of any grade of coagulopathy/deep-vein thrombosis and gastrointestinal disorders was significantly higher in the MTX cohort than in the TEN cohort; no significant difference was found in the incidence of other adverse events between the two cohorts.

conclusionsThis was the first multicenter study using TEN as the main agent compared with HD-MTX in newly diagnosed primary CNS lymphoma. The TEN-based regimen was non-inferior to the HD-MTX-based regimen with similar overall responses. CLASSIFICATION OF EVIDENCE: This study provided Class III evidence that the teniposide-based regimen was non-inferior to high-dose methotrexate - based regimen with similar overall responses and long-time survival in immunocompetent patients with PCNSL.

Indexed as

Central Nervous System NeoplasmsLymphomaAdultAntineoplastic Combined Chemotherapy ProtocolsCentral Nervous SystemHumansInduction ChemotherapyMethotrexateRetrospective StudiesTeniposideMethotrexateTeniposideFirst-line induction chemotherapyMethotrexatePrimary central nervous system lymphomaTeniposide

Identifiers

PMID37568079
PMCPMC10416388
OpenAlexW4385763642

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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.