Evidence map›Paper›PMID 33402163›Full record

ArticleDiagnostic pathology2021

The clinicopathological relevance of uniform CD56 expression in anaplastic large cell lymphoma: a retrospective analysis of 18 cases.

Bao-Hua Yu, Yan Zhang, Tian Xue, Ruo-Hong Shui, Hong-Fen Lu, Xiao-Yan Zhou, Xiong-Zeng Zhu, Xiao-Qiu Li

Abstract read
In one paragraph

Article in Diagnostic pathology, 2021. 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
–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

8 citing papers in PubMed.

  1. Review
  2. CD56 on immune and tumor cells: what is known and beyond?Clinical and experimental immunology · 2025
    Review
  3. Article
  4. Circular RNAs: characteristics, functions, mechanisms, and potential applications in thyroid cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
  5. Review
  6. Review
  7. Review
  8. Review
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.

Bao-Hua YuDepartment of Pathology, Fudan University Shanghai Cancer Center, 270 Dong-an Road, Xuhui District, Shanghai, 200032, China.
Yan ZhangDepartment of Pathology, Fudan University Shanghai Cancer Center, 270 Dong-an Road, Xuhui District, Shanghai, 200032, China.
Tian XueDepartment of Pathology, Fudan University Shanghai Cancer Center, 270 Dong-an Road, Xuhui District, Shanghai, 200032, China.
Ruo-Hong ShuiDepartment of Pathology, Fudan University Shanghai Cancer Center, 270 Dong-an Road, Xuhui District, Shanghai, 200032, China.
Hong-Fen LuDepartment of Pathology, Fudan University Shanghai Cancer Center, 270 Dong-an Road, Xuhui District, Shanghai, 200032, China.
Xiao-Yan ZhouDepartment of Pathology, Fudan University Shanghai Cancer Center, 270 Dong-an Road, Xuhui District, Shanghai, 200032, China.
Xiong-Zeng ZhuDepartment of Pathology, Fudan University Shanghai Cancer Center, 270 Dong-an Road, Xuhui District, Shanghai, 200032, China.
Xiao-Qiu LiDepartment of Pathology, Fudan University Shanghai Cancer Center, 270 Dong-an Road, Xuhui District, Shanghai, 200032, China. leexiaoqiu@hotmail.com.

Funding

Shanghai Science and Technology Development Fund 19MC1911000the Youth Project of National Nature Science Funding of China 81700195
6 · The paper itself

Abstract

backgroundAnaplastic large cell lymphoma (ALCL) with uniform CD56 expression is a rare condition, that has been described in limited literature, and its clinicopathological features have not yet been well illustrated. The aim of our study was to fully investigate the clinical, histological, immunohistochemical and molecular features of CD56+ ALCL.

methodsThe clinical and histological characteristics of CD56+ ALCL cases were retrospectively evaluated. The immunohistochemical phenotype, status of Epstein-Barr virus (EBV) and T-cell receptor (TCR) gene rearrangement were examined. Overall survival was also analyzed.

resultsEighteen (5.8%) cases with diffuse CD56 expression were identified out of 313 archived ALCL cases with CD56 test. CD56 expression was significantly higher in ALK+ systemic ALCLs (sALCLs) (13/64, 20.3%) than in ALK- sALCLs (3/101, 3.0%) (p < 0.001) as well as primary cutaneous ALCLs (2/148, 1.4%) (p < 0.001). Regarding the CD56+ ALK+ sALCLs, the median age was 20 years (range, 8-60 years) with a male-to-female ratio of 2.3:1, and these cases more frequently affected extranodal sites (11/38, 28.9%) rather than lymph nodes (2/26, 7.7%) (p = 0.038). Eleven (84.6%) cases presented with stage I-II diseases, which was significantly more than their CD56- ALK+ counterparts (45.5%) (p = 0.015). Histologically, 2 ALK+ cases were of small cell variant and all the others displayed characteristic morphology of classic ALCL. Regarding the immunophenotype, both CD30 and CD56 were diffusely positive in all cases. CD3, CD43, anaplastic lymphoma kinase-1 (ALK1), TIA-1, EMA expression was observed in 30.8% (4/13), 90.9% (10/11), 100% (13/13), 100% (9/9), and 80.0% (8/10) cases, respectively. EBV infection was consistently absent. Monoclonal TCR gene rearrangement was found in 100% (5/5) of investigated ALK+ cases. Chemotherapy with a CHOP regimen was most frequently employed. The 3-year overall survival (OS) rate for CD56+ ALK+ patients was 92.0%, compared with 73.0% for their CD56- counterparts, but there was no significant difference in OS between the two groups (p = 0.264).

conclusionsUniform CD56 expression is an unexpected condition in ALCL. Of ALK+ ALCLs, CD56 expression correlated with a high frequency of early stage and an extranodal predominance. It is of great importance to raise awareness of this condition and familiarity with its characteristic features to avoid diagnostic and therapeutic pitfalls. Further investigations are warranted for a better understanding of this unusual phenotype and the significance of CD56 expression in ALCL.

Indexed as

AdolescentAdultCD56 AntigenChildDiagnosis, DifferentialFemaleGene RearrangementGenes, T-Cell ReceptorHumansImmunohistochemistryImmunophenotypingLymphoma, Large-Cell, AnaplasticMaleMiddle AgedPhenotypeRetrospective StudiesCD56 AntigenNCAM1 protein, humanALKAnaplastic large cell lymphomaCD56 expressionDifferential diagnosisOverall survival

Identifiers

PMID33402163
PMCPMC7786455

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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.