Evidence map›Paper›PMID 32619037›Full record

ArticleCancer science2020

Clinical utility of target capture-based panel sequencing in hematological malignancies: A multicenter feasibility study.

Takahiko Yasuda, Masashi Sanada, Dai Nishijima, Takashi Kanamori, Yuka Iijima, Hiroyoshi Hattori, Akiko Saito, Hiroaki Miyoshi, Yuichi Ishikawa, Norio Asou and 27 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Cancer science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Clinical features ofTherapeutic advances in hematology · 2021
    Review
  10. Article
  11. Article
  12. 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

37 authors at 19 institutions in 3 countries.

Takahiko YasudaClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.ORCID https://orcid.org/0000-0002-4686-0976
Masashi SanadaClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Dai NishijimaClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Takashi KanamoriClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Yuka IijimaClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Hiroyoshi HattoriClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Akiko SaitoClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Hiroaki MiyoshiDepartment of Pathology, Kurume University School of Medicine, Kurume, Japan.ORCID https://orcid.org/0000-0002-2356-3725
Yuichi IshikawaDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Norio AsouDepartment of Hematology, Comprehensive Cancer Center, International Medical Center, Saitama Medical University, Saitama, Japan.
Kensuke UsukiDepartment of Hematology, NTT Medical Center Tokyo, Tokyo, Japan.
Shinsuke HirabayashiDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Motohiro KatoDepartment of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, Tokyo, Japan.
Masaki RiDepartment of Hematology and Oncology, Nagoya City University Institute of Medical and Pharmaceutical Science, Nagoya, Japan.ORCID https://orcid.org/0000-0002-9617-486X
Hiroshi HandaDepartment of Hematology, Gunma University Graduate School of Medicine, Maebashi, Japan.
Tadao IshidaDepartment of Hematology, Japanese Red Cross Medical Center, Tokyo, Japan.ORCID https://orcid.org/0000-0003-3219-3292
Hirohiko ShibayamaDepartment of Hematology and Oncology, Osaka University Graduate School of Medicine, Osaka, Japan.
Masahiro AbeDepartment of Hematology, Endocrinology and Metabolism, Tokushima University Graduate School, Tokushima, Japan.
Chisako IriyamaDepartment of Hematology, Fujita Health University, Toyoake, Japan.
Kennosuke KarubeDepartment of Pathology and Cell Biology, Graduate School of Medicine and Faculty of Medicine, University of the Ryukyus, Okinawa, Japan.ORCID https://orcid.org/0000-0002-1205-858X
Momoko NishikoriDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0003-4171-2162
Koichi OhshimaDepartment of Pathology, Kurume University School of Medicine, Kurume, Japan.
Keisuke KataokaDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.
Kenichi YoshidaDepartment of Pathology and Tumor biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Yuichi ShiraishiDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Hiroaki GotoDivision of Hemato-Oncology and Regenerative Medicine, Kanagawa Children's Medical Center, Yokohama, Japan.
Souichi AdachiDepartment of Human Health Science, Kyoto University, Kyoto, Japan.
Ryoji KobayashiDepartment of Pediatrics, Sapporo Hokuyu Hospital, Sapporo, Japan.
Hitoshi KiyoiDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID https://orcid.org/0000-0001-6382-9498
Yasushi MiyazakiDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University, Nagasaki, Japan.
Seishi OgawaDepartment of Pathology and Tumor biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Hiroki KurahashiDivision of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.
Hisayuki YokoyamaDepartment of Hematology, National Hospital Organization, Sendai Medical Center, Sendai, Japan.
Atsushi ManabeDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Shinsuke IidaDepartment of Hematology and Oncology, Nagoya City University Institute of Medical and Pharmaceutical Science, Nagoya, Japan.ORCID https://orcid.org/0000-0002-4951-960X
Akihiro TomitaDepartment of Hematology, Fujita Health University, Toyoake, Japan.
Keizo HoribeClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
National Hospital Organization · JPKyoto University · JPFujita Health University · JPNagoya City University · JPHokkaido University · JPKurume University · JPNagoya University · JPGunma University · JPJapanese Red Cross Medical Center · JPKanagawa Children's Medical Center · JPNagasaki University · JPNational Center For Child Health and Development · JPNTT Medical Center · JPSaitama International Medical Center · JPSapporo Hokuyu Hospital · JPSendai Medical Center · JPThe University of Osaka · JPTokushima University · JPUniversity of the Ryukyus · JP

Funding

AMED 18kk0205005h003AMED JPAMED JP20cm0106501h0005JSPS KAKENHI JP19H05656JSPS KAKENHI JP26221308
6 · The paper itself

Abstract

Although next-generation sequencing-based panel testing is well practiced in the field of cancer medicine for the identification of target molecules in solid tumors, the clinical utility and clinical issues surrounding panel testing in hematological malignancies have yet to be fully evaluated. We conducted a multicenter prospective clinical sequencing study to verify the feasibility of a panel test for hematological tumors, including acute myeloid leukemia, acute lymphoblastic leukemia, multiple myeloma, and diffuse large B-cell lymphoma. Out of 96 eligible patients, 79 patients (82%) showed potentially actionable findings, based on the clinical sequencing assays. We identified that genetic alterations with a strong clinical significance were found at a higher frequency in terms of diagnosis (n = 60; 63%) and prognosis (n = 61; 64%) than in terms of therapy (n = 8; 8%). Three patients who harbored a germline mutation in either DDX41 (n = 2) or BRCA2 (n = 1) were provided with genetic counseling. At 6 mo after sequencing, clinical actions based on the diagnostic (n = 5) or prognostic (n = 3) findings were reported, but no patients were enrolled in a clinical trial or received targeted therapies based on the sequencing results. These results suggest that panel testing for hematological malignancies would be feasible given the availability of useful diagnostic and prognostic information. This study is registered with the UMIN Clinical Trial Registry (UMIN000029879, multiple myeloma; UMIN000031343, adult acute myeloid leukemia; UMIN000033144, diffuse large B-cell lymphoma; and UMIN000034243, childhood leukemia).

Indexed as

Biomarkers, TumorGenetic Association StudiesGenetic Predisposition to DiseaseAdolescentAdultAgedAged, 80 and overChildChild, PreschoolComputational BiologyFemaleGenetic TestingGerm-Line MutationHematologic NeoplasmsHigh-Throughput Nucleotide SequencingHumansBiomarkers, Tumorclinical sequencingfeasibility studyhematological malignancypanel testingpotentially actionable finding

Identifiers

PMID32619037
PMCPMC7469806
OpenAlexW3038720113

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.