Evidence map›Paper›PMID 36229495›Full record

ArticleNPJ systems biology and applications2022

Early dynamics of chronic myeloid leukemia on nilotinib predicts deep molecular response.

Yuji Okamoto, Mitsuhito Hirano, Kai Morino, Masashi K Kajita, Shinji Nakaoka, Mayuko Tsuda, Kei-Ji Sugimoto, Shigehisa Tamaki, Junichi Hisatake, Hisayuki Yokoyama and 11 more

Open access · goldAbstract read
In one paragraph

Article in NPJ systems biology and applications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

4 citing papers in PubMed, 3 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

21 authors at 18 institutions in 1 country.

Yuji Okamoto *Institute of Industrial Science, The University of Tokyo, Tokyo, 153-8505, Japan.
Mitsuhito Hirano *Division of Molecular Therapy, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan.
Kai MorinoInstitute of Industrial Science, The University of Tokyo, Tokyo, 153-8505, Japan.
Masashi K KajitaInstitute of Industrial Science, The University of Tokyo, Tokyo, 153-8505, Japan. masashi.k.kajita@gmail.com.ORCID 0000-0002-2939-2058
Shinji NakaokaInstitute of Industrial Science, The University of Tokyo, Tokyo, 153-8505, Japan.ORCID 0000-0002-3277-9552
Mayuko TsudaDivision of Molecular Therapy, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan.
Kei-Ji SugimotoDivision of Hematology, Juntendo University Urayasu Hospital, Chiba, 279-0021, Japan.
Shigehisa TamakiDepartment of Hematology, Japanese Red Cross Ise Hospital, Mie, 516-8512, Japan.
Junichi HisatakeDepartment of Hematology, Japanese Red Cross Omori Hospital, Tokyo, 143-8527, Japan.
Hisayuki YokoyamaDepartment of Hematology, National Hospital Organization, Sendai Medical Center, Miyagi, 983-8520, Japan.ORCID 0000-0001-7658-0687
Tadahiko IgarashiDivison of Hematology and Oncology, Gunma Cancer Center, Gunma, 373-8550, Japan.
Atsushi ShinagawaDepartment of Internal Medicine, Hitachi General Hospital, Ibaraki, 317-0077, Japan.
Takeaki SugawaraDivision of Hematology-Oncology, Chiba Cancer Center, Chiba, 260-8717, Japan.
Satoru HaraDepartment of Hematology, Chiba Rosai Hospital, Chiba, 290-0003, Japan.
Kazuhisa FujikawaDepartment of Hematology, Chibaken Saiseikai Narashino Hospital, Chiba, 275-8580, Japan.
Seiichi ShimizuDepartment of Hematology, Tsuchiura Kyodo General Hospital, Ibaraki, 300-0028, Japan.
Toshiaki YujiriThird Department of Internal Medicine, Yamaguchi University, Yamaguchi, 755-0046, Japan.ORCID 0000-0001-6838-3456
Hisashi WakitaDivision of Hematology and Oncology, Japanese Red Cross Narita Hospital, Chiba, 286-8523, Japan.
Kaichi NishiwakiDivision of Oncology and Hematology, Jikei University Kashiwa Hospital, Chiba, 277-8567, Japan.
Arinobu TojoDivision of Molecular Therapy, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan.
Kazuyuki AiharaInstitute of Industrial Science, The University of Tokyo, Tokyo, 153-8505, Japan. kaihara@g.ecc.u-tokyo.ac.jp.
The University of Tokyo · JPChiba Cancer Center · JPChibaken Saiseikai Narashino Hospital · JPChiba Rosai Hospital · JPGunma Children's Medical Center · JPHitachi General Hospital · JPHokkaido University · JPIse Red Cross Hospital · JPJapanese Red Cross Narita Hospital · JPJikei University Kashiwa hospital · JPJuntendo University Urayasu Hospital · JPKyoto University · JPKyushu University · JPSendai Medical Center · JPTokyo Medical and Dental University · JPTsuchiura Kyodo General Hospital · JPUniversity of Fukui · JPYamaguchi University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic myeloid leukemia (CML) is a myeloproliferative disorder caused by the BCR-ABL1 tyrosine kinase. Although ABL1-specific tyrosine kinase inhibitors (TKIs) including nilotinib have dramatically improved the prognosis of patients with CML, the TKI efficacy depends on the individual patient. In this work, we found that the patients with different nilotinib responses can be classified by using the estimated parameters of our simple dynamical model with two common laboratory findings. Furthermore, our proposed method identified patients who failed to achieve a treatment goal with high fidelity according to the data collected only at three initial time points during nilotinib therapy. Since our model relies on the general properties of TKI response, our framework would be applicable to CML patients who receive frontline nilotinib or other TKIs.

Indexed as

Leukemia, Myelogenous, Chronic, BCR-ABL PositiveProtein Kinase InhibitorsFusion Proteins, bcr-ablHumansPyrimidinesFusion Proteins, bcr-ablnilotinibProtein Kinase InhibitorsPyrimidines

Identifiers

PMID36229495
PMCPMC9561725
OpenAlexW4304891595

What OpenQuestion 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 OpenQuestion graph.