Evidence map›Paper›PMID 26588928›Full record

ArticleInternational journal of hematology2016

SF3B1 and IGHV gene mutation status predict poor prognosis in Japanese CLL patients.

Takeki Mitsui, Hiromi Koiso, Hirotaka Nakahashi, Akio Saitoh, Hiroaki Shimizu, Takuma Ishizaki, Yoshiyuki Ogawa, Makiko Takizawa, Akihiko Yokohama, Takayuki Saitoh and 9 more

Abstract read
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In one paragraph

Article in International journal of hematology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Observational
  5. Oncotarget · 2017
    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

19 authors at 6 institutions in 1 country.

Takeki MitsuiDepartment of Medicine and Clinical Sciences, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan. mitsuit@gunma-u.ac.jp.
Hiromi KoisoOncology Center, Gunma University Hospital, Maebashi, Japan.
Hirotaka NakahashiDepartment of Medicine and Clinical Sciences, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan.
Akio SaitohFujioka General Hospital, Fujioka, Japan.
Hiroaki ShimizuDepartment of Medicine and Clinical Sciences, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan.
Takuma IshizakiDepartment of Medicine and Clinical Sciences, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan.
Yoshiyuki OgawaDepartment of Medicine and Clinical Sciences, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan.
Makiko TakizawaDepartment of Medicine and Clinical Sciences, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan.
Akihiko YokohamaDepartment of Blood Transfusion Service, Gunma University Hospital, Maebashi, Japan.
Takayuki SaitohDepartment of Laboratory Sciences, Gunma University Graduate School of Health Science, Maebashi, Japan.
Takahiro JinboFujioka General Hospital, Fujioka, Japan.
Hidemi OguraMaebashi Red Cross Hospital, Maebashi, Japan.
Hiroshi HandaDepartment of Medicine and Clinical Sciences, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan.
Morio SawamuraNational Hospital Organization, Nishigunma National Hospital, Shibukawa, Japan.
Tohru SakuraSaiseikai Maebashi Hospital, Maebashi, Japan.
Masamitsu KarasawaUsui Hospital, Annaka, Japan.
Hirokazu MurakamiDepartment of Laboratory Sciences, Gunma University Graduate School of Health Science, Maebashi, Japan.
Yoshihisa NojimaDepartment of Medicine and Clinical Sciences, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan.
Norifumi TsukamotoOncology Center, Gunma University Hospital, Maebashi, Japan.
Gunma University · JPGunma University Hospital · JPShizuoka General Hospital · JPGunma Saiseikai Maebashi Hospital · JPMaebashi Red Cross Hospital · JPNational Hospital Organization · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The incidence of chronic lymphocytic leukemia (CLL) is low in Japan. The clinical course ranges from very indolent to rapidly progressive. Recently, several reports have indicated that mutation of the splicing factor 3b, subunit 1 (SF3B1) gene in CLL is predictive of a poor prognosis. Here, we investigated the SF3B1 mutational status of Japanese CLL patients and clarified the association between SF3B1 mutational status and prognostic factors. One hundred and two patients that were referred to our institutions between 1999 and 2013 were enrolled. Mutation analysis of SF3B1 (n = 87) and of the immunoglobulin heavy chain gene (IGHV) (n = 102) was performed at diagnosis. FISH analysis of del(11)(q22) was performed for 17 patients. Seven patients have SF3B1 mutation (8.0 %: K700E, 5/7; G742D, 1/7 and Y623C, 1/7). The median survival times for patients with mutated and non-mutated SF3B1 were 53 and 130 months, respectively. Overall survival of the mutated SF3B1 group was significantly lower than that of the non-mutated group (p = 0.0187). No relationship was observed between IGHV mutational status and SF3B1 mutation. There was no patient with SF3B1 mutation in the IGHV1-69 population (0/2). In conclusion, mutation of SF3B1 at diagnosis in Japanese CLL patients is predictive of a poor prognosis.

Indexed as

MutationAdultAgedAged, 80 and overAsian PeopleDisease ProgressionFemaleHumansImmunoglobulin Heavy ChainsLeukemia, Lymphocytic, Chronic, B-CellMaleMiddle AgedPhosphoproteinsPredictive Value of TestsPrognosisRNA Splicing FactorsImmunoglobulin Heavy ChainsPhosphoproteinsRNA Splicing FactorsSF3B1 protein, humanChronic lymphocytic leukemiaIGHV mutational statusSF3B1

Identifiers

PMID26588928
OpenAlexW2177152105

What OpenQuestion holds

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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.