Evidence map›Paper›PMID 36522654›Full record

ArticleBMC medicine2022

Clinicopathologic features and abnormal signaling pathways in plasmablastic lymphoma: a multicenter study in China.

Di Shi, Lin Gao, Xiao-Chun Wan, Jin Li, Tian Tian, Jue Hu, Qun-Ling Zhang, Yi-Fan Su, Yu-Peng Zeng, Zi-Juan Hu and 5 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in BMC medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 13 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

15 authors at 6 institutions in 1 country.

Di ShiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Lin GaoGenePlus-Shenzhen, Shenzhen, 518000, People's Republic of China.
Xiao-Chun WanDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Jin LiDepartment of Oncology, Hunan Cancer Hospital, Changsha, 410000, China.
Tian TianDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Jue HuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Qun-Ling ZhangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Yi-Fan SuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Yu-Peng ZengDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Zi-Juan HuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Bao-Hua YuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Xiao-Qiu LiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Ping WeiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Ji-Wei LiDepartment of Oncology, The Second Xiangya Hospital, Central South University, Changsha, China. lijiwei2021@csu.edu.cn.
Xiao-Yan ZhouDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. xyzhou100@163.com.
Fudan University · CNFudan University Shanghai Cancer Center · CNShanghai Medical College of Fudan University · CNCentral South University · CNHunan Cancer Hospital · CNShenzhen Bioeasy Biotechnology (China) · CN

Funding

National Natural Science Foundation of China 81470353National Natural Science Foundation of China 81700195National Natural Science Foundation of China 81870155
6 · The paper itself

Abstract

backgroundPlasmablastic lymphoma (PBL) is a rare but aggressive B-cell lymphoma subtype with poor prognosis. Knowledge about the etiology, clinicopathologic and molecular features, and outcomes of PBL is limited. This study aimed to examine the clinicopathologic characteristics, therapeutic approaches, and clinical outcomes of PBL patients in a Chinese population.

methodsA total of 102 PBL patients were recruited from three cancer centers. The pathologic features and clinical outcomes of 56 patients with available treatment details and follow-up data were reviewed and analyzed. RNA sequencing was performed in 6 PBL and 11 diffuse large B-cell lymphoma (DLBCL) patients.

resultsMost patients in our cohort were male (n = 36, 64.3%), and 35 patients presented with Ann Arbor stage I/II disease at diagnosis. All these patients showed negative findings for human immunodeficiency virus, and the vast majority of patients in our cohort were immunocompetent. Lymph nodes (n = 13, 23.2%) and gastrointestinal tract (n = 10, 17.9%) were the most commonly involved site at presentation. Post-treatment complete remission (CR) was the only prognostic factor affecting overall survival (OS) and progression-free survival (PFS) in the multivariate analysis. RNA-seq demonstrated that B-cell receptor (BCR), T-cell receptor (TCR), P53, calcium signaling, and Wnt signaling pathways were significantly downregulated in PBLs compared with GCB (or non-GCB) DLBCLs.

conclusionsIn this multicenter study in the Chinese population, PBL mainly occurred in immunocompetent individuals and most patients present with early-stage disease at diagnosis. Post-treatment CR was an important prognostic factor affecting OS and PFS. RNA-seq showed that the B-cell receptor (BCR), P53, calcium signaling, cell adhesion molecules, and Wnt signaling pathways significantly differed between PBL and GCB (or non-GCB) DLBCL, which provided theoretical basis for its pathogenesis and future treatment.

Indexed as

Plasmablastic LymphomaFemaleHumansMalePrognosisReceptors, Antigen, B-CellSignal TransductionTumor Suppressor Protein p53Receptors, Antigen, B-CellTumor Suppressor Protein p53ImmunocompetentPlasmablastic lymphomaRNA-sequencing

Identifiers

PMID36522654
PMCPMC9753322
OpenAlexW4311611286

What Socratic holds

Textmetadata
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 Socratic graph.