Evidence map›Paper›PMID 26131212›Full record

ArticleInternational journal of clinical and experimental medicine2015

Association of SLCO1B1 gene polymorphisms with toxicity response of high dose methotrexate chemotherapy in childhood acute lymphoblastic leukemia.

Jun Li, Xiao-Ru Wang, Xiao-Wen Zhai, Hong-Sheng Wang, Xiao-Wen Qian, Hui Miao, Xiao-Hua Zhu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Genetic markers in methotrexate treatments.The pharmacogenomics journal · 2018
    Pooled it
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. 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

7 authors at 2 institutions in 1 country.

Jun LiDepartment of Hematology and Oncology, Children's Hospital of Fudan University No. 399 Wanyuan Road, Shanghai, 201102, P.R. China.
Xiao-Ru WangDepartment of Pediatries, Provincial Hospital Affiliated to Shandong University 324 Jingwu Road, Jinan, Shandong 250021, China.
Xiao-Wen ZhaiDepartment of Hematology and Oncology, Children's Hospital of Fudan University No. 399 Wanyuan Road, Shanghai, 201102, P.R. China.
Hong-Sheng WangDepartment of Hematology and Oncology, Children's Hospital of Fudan University No. 399 Wanyuan Road, Shanghai, 201102, P.R. China.
Xiao-Wen QianDepartment of Hematology and Oncology, Children's Hospital of Fudan University No. 399 Wanyuan Road, Shanghai, 201102, P.R. China.
Hui MiaoDepartment of Hematology and Oncology, Children's Hospital of Fudan University No. 399 Wanyuan Road, Shanghai, 201102, P.R. China.
Xiao-Hua ZhuDepartment of Hematology and Oncology, Children's Hospital of Fudan University No. 399 Wanyuan Road, Shanghai, 201102, P.R. China.
Children's Hospital of Fudan University · CNShandong Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe present study aims to investigate the correlation of polymorphisms of SLCO1B1 gene with the toxicity during therapy with the high-dose methotrexate (MTX) chemotherapy in childhood acute lymphoblastic leukemia.

methodsWe analyzed 2 polymorphisms (rs4149081 and rs11045897) in SLCO1B1 gene in 280 Chinese pediatric B-ALL patients, using MTX plasma concentration as an objective and quantifiable marker of toxicity. We utilized Enzyme-multiplied immunoassay technique (EMIT) to measure the plasma concentration of MTX. The polymerase chain reaction-allele specific (PCR-AS) method was utilized to perform the genotyping.

resultsWe found there was a statistically significant association between MTX plasma concentration and the SLCO1B1 rs11045879 CC genotype (P<0.05). We also found the rs4149081 AA genotype was associated with high-MTX plasma concentrations. A-C haplotype carriers have a higher risk for MTX delayed clearance but G-T haplotype was associated with a lower risk for MTX delayed clearance.

conclusionsThe rs4149081 AA genotype and the rs11045897 CC genotype could be indicators for high-MTX plasma concentrations in children with ALL.

Indexed as

Acute lymphoblastic leukemiamethotrexateSLCO1B1toxicity

Identifiers

PMID26131212
PMCPMC4483916
OpenAlexW2405317953

What OpenQuestion holds

Textmetadata
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.