Evidence map›Paper›PMID 35579198›Full record

ArticleCancer science2022

Feasibility and clinical utility of comprehensive genomic profiling of hematological malignancies.

Suguru Fukuhara, Yuji Oshikawa-Kumade, Yasunori Kogure, Sumito Shingaki, Hirokazu Kariyazono, Yoshiya Kikukawa, Junji Koya, Yuki Saito, Mariko Tabata, Kota Yoshifuji and 19 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Molecular pathogenesis and evolving treatment landscape of extranodal NK/T-cell lymphoma.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2026
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. 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

29 authors at 7 institutions in 1 country.

Suguru FukuharaDepartment of Hematology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-2423-9978
Yuji Oshikawa-KumadeDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0003-1959-6038
Yasunori KogureDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0003-1158-5131
Sumito ShingakiDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-4249-5000
Hirokazu KariyazonoDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.
Yoshiya KikukawaDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.
Junji KoyaDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-0605-1226
Yuki SaitoDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0003-2686-9604
Mariko TabataDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-8013-7327
Kota YoshifujiDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.
Kota MizunoDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.
Akiko Miyagi-MaeshimaDepartment of Pathology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0001-7251-7920
Hiromichi MatsushitaDepartment of Laboratory Medicine, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-1629-6630
Masanaka SugiyamaDepartment of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0003-0691-0331
Chitose OgawaDepartment of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
Yoshihiro InamotoDepartment of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4881-0427
Takahiro FukudaDepartment of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
Masato SuganoDepartment of Pathology and Clinical Laboratories, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0003-2695-8172
Nobuhiko YamauchiDepartment of Hematology and Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Yosuke MinamiDepartment of Hematology and Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0003-0863-0739
Makoto HirataGenetic Medicine and Services, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-9994-9958
Teruhiko YoshidaGenetic Medicine and Services, National Cancer Center Hospital, Tokyo, Japan.
Takashi KohnoDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-5371-706X
Shinji KohsakaDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0001-8651-6136
Hiroyuki ManoDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4645-0181
Yuichi ShiraishiDivision of Genome Analysis Platform Development, National Cancer Center Research Institute, Tokyo, Japan.
Seishi OgawaDepartment of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Koji IzutsuDepartment of Hematology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0001-9129-8057
Keisuke KataokaDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-8263-9902
Tokyo National Hospital · JPKeio University · JPNational Cancer Center Hospital East · JPOtsuka (Japan) · JPKyoto University · JPThe University of Tokyo · JPTokyo Medical and Dental University · JP

Funding

National Cancer Center Research and Development Funds 30-A-1Otsuka Pharmaceutical Co., Ltd.
6 · The paper itself

Abstract

Identification of genetic alterations through next-generation sequencing (NGS) can guide treatment decision-making by providing information on diagnosis, therapy selection, and prognostic stratification in patients with hematological malignancies. Although the utility of NGS-based genomic profiling assays was investigated in hematological malignancies, no assays sufficiently cover driver mutations, including recently discovered ones, as well as fusions and/or pathogenic germline variants. To address these issues, here we have devised an integrated DNA/RNA profiling assay to detect various types of somatic alterations and germline variants at once. Particularly, our assay can successfully identify copy number alterations and structural variations, including immunoglobulin heavy chain translocations, IKZF1 intragenic deletions, and rare fusions. Using this assay, we conducted a prospective study to investigate the feasibility and clinical usefulness of comprehensive genomic profiling for 452 recurrently altered genes in hematological malignancies. In total, 176 patients (with 188 specimens) were analyzed, in which at least one alteration was detected in 171 (97%) patients, with a median number of total alterations of 7 (0-55). Among them, 145 (82%), 86 (49%), and 102 (58%) patients harbored at least one clinically relevant alteration for diagnosis, treatment, and prognosis, respectively. The proportion of patients with clinically relevant alterations was the highest in acute myeloid leukemia, whereas this assay was less informative in T/natural killer-cell lymphoma. These results suggest the clinical utility of NGS-based genomic profiling, particularly for their diagnosis and prognostic prediction, thereby highlighting the promise of precision medicine in hematological malignancies.

Indexed as

Hematologic NeoplasmsHigh-Throughput Nucleotide SequencingFeasibility StudiesGenomicsHumansMutationProspective Studiescomprehensive genomic profilinghematological malignancynext-generation sequencingprecision medicinesomatic alteration

Identifiers

PMID35579198
PMCPMC9357666
OpenAlexW4280580737

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.