Evidence map›Paper›PMID 40686686›Full record

ArticleEClinicalMedicine2025

Treatment outcomes for patients with newly diagnosed or relapsed/refractory TP53-mutated mantle cell lymphoma: a systematic review and meta-analysis.

Na Zhang, Jiegang Xu, Chengxin Luo, Rushuang Xu, Yan Zeng, Dongfeng Zeng, Shuangnian Xu, Xi Li

Abstract read
In one paragraph

Article in EClinicalMedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Na ZhangDepartment of Hematology, Chongqing Key Laboratory of Hematology and Microenvironment, Army Medical Center, Daping Hospital, Army Medical University of PLA, Chongqing, China.
Jiegang XuDepartment of Hematology, Southwest Hospital, Army Medical University of PLA, Chongqing, China.
Chengxin LuoDepartment of Hematology, Southwest Hospital, Army Medical University of PLA, Chongqing, China.
Rushuang XuDepartment of Hematology, Chongqing Key Laboratory of Hematology and Microenvironment, Army Medical Center, Daping Hospital, Army Medical University of PLA, Chongqing, China.
Yan ZengDepartment of Hematology, Chongqing Key Laboratory of Hematology and Microenvironment, Army Medical Center, Daping Hospital, Army Medical University of PLA, Chongqing, China.
Dongfeng ZengDepartment of Hematology, Chongqing Key Laboratory of Hematology and Microenvironment, Army Medical Center, Daping Hospital, Army Medical University of PLA, Chongqing, China.
Shuangnian XuDepartment of Hematology, Southwest Hospital, Army Medical University of PLA, Chongqing, China.
Xi LiDepartment of Hematology, Chongqing Key Laboratory of Hematology and Microenvironment, Army Medical Center, Daping Hospital, Army Medical University of PLA, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: TP53 mutation is a critical predictor of early disease progression and poor prognosis in mantle cell lymphoma (MCL). Optimal treatment for these patients remains unclear. This systematic review and meta-analysis evaluated various strategies for achieving remission in TP53-mutated (TP53m) MCL. Methods: We searched EMBASE, MEDLINE and conference proceedings from inception to May 7, 2025, without language restrictions. Randomised controlled trials, single-arm trials, and prospective or retrospective observational studies assessing remission strategies in newly diagnosed or relapsed/refractory TP53m MCL were included. Case reports, case series, and non-human studies were excluded. Two authors independently selected studies, extracted summary data from published reports, and assessed bias risk. Outcomes of interest were complete remission (CR) rate, overall response rate (ORR), overall survival (OS), and progression-free survival (PFS). Random-effects meta-analyses were used for summary estimation. The study is registered with PROSPERO, CRD42024594152. Findings: A total of 9833 studies were identified, of which 39 studies involving 734 patients with TP53m MCL were eligible. For newly diagnosed TP53m MCL, targeted therapy (TT) had a CR rate of 89% (95% confidence interval (CI) 80-99; n = 52; I Interpretation: Our findings indicate that TT may benefit patients with newly diagnosed TP53m MCL, and Allo-HSCT, CAR-T cell therapy, or TT could be considered for relapsed/refractory cases. However, -suboptimal long-term survival highlights the urgent need for innovative therapies. Key limitations, including small sample sizes and few randomised controlled trials (RCTs), emphasize the need for well-designed RCTs with adequate sample size in this field. Funding: The Chongqing Natural Science Foundation and Talent Innovation Capability Cultivation Program of the Army Medical Center.

Indexed as

Mantle cell lymphomaRemission strategiesTP53 mutations

Identifiers

PMID40686686
PMCPMC12274854

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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.