Evidence map›Paper›PMID 35876224›Full record

ReviewCancer science2022

Expert panel consensus recommendations on the use of circulating tumor DNA assays for patients with advanced solid tumors.

Mitsuho Imai, Yoshiaki Nakamura, Kuniko Sunami, Hidenori Kage, Keigo Komine, Takafumi Koyama, Toraji Amano, Daisuke Ennishi, Masashi Kanai, Hirotsugu Kenmotsu and 11 more

Open access · goldAbstract readReviewConsensus Statement
In one paragraph

Review in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 12 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 13 institutions in 2 countries.

Mitsuho ImaiTranslational Research Support Section, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0001-8736-0399
Yoshiaki NakamuraTranslational Research Support Section, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0002-5241-6855
Kuniko SunamiDepartment of Laboratory Medicine, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-7137-5649
Hidenori KageDepartment of Next-Generation Precision Medicine Development Laboratory, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0003-3658-4442
Keigo KomineDepartment of Medical Oncology, Tohoku University Hospital, Sendai, Japan.
Takafumi KoyamaDepartment of Experimental Therapeutics, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0001-5807-8458
Toraji AmanoClinical Research and Medical Innovation Center, Hokkaido University Hospital, Hokkaido, Japan.
Daisuke EnnishiCenter for Comprehensive Genomic Medicine, Okayama University Hospital, Okayama, Japan.
Masashi KanaiDepartment of Therapeutic Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0002-6954-4474
Hirotsugu KenmotsuDivision of Thoracic Oncology, Shizuoka Cancer Center, Suntougun, Japan.ORCID https://orcid.org/0000-0003-0590-9259
Takahiro MaedaDivision of Precision Medicine, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Sachi MoritaDepartment of Clinical Oncology and Chemotherapy, Nagoya University Hospital, Nagoya, Japan.ORCID https://orcid.org/0000-0002-3115-2336
Daisuke SakaiCenter for Cancer Genomics and Personalized Medicine, Osaka University Hospital, Suita, Japan.
Hideaki BandoTranslational Research Support Section, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0001-5041-2765
Akitaka MakiyamaCancer Center, Gifu University Hospital, Gifu, Japan.
Tatsuya SuzukiDepartment of Hematology, National Cancer Center Hospital, Tokyo, Japan.
Makoto HirataDepartment of Genetic Medicine and Services, National Cancer Center Hospital, Tokyo, Japan.
Shinji KohsakaDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0001-8651-6136
Katsuya TsuchiharaDivision of Translational Informatics, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa, Japan.ORCID https://orcid.org/0000-0001-7507-2349
Yoichi NaitoDepartment of General Internal Medicine/Experimental Therapeutics/Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0002-8490-9064
Takayuki YoshinoTranslational Research Support Section, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0002-0489-4756
National Cancer Center Hospital East · JPTokyo National Hospital · JPGifu University Hospital · JPHokkaido University Hospital · JPKeio University · JPKyoto University · JPKyushu University · JPNagoya University Hospital · JPOkayama University Hospital · JPOsaka University Hospital · JPPrecision Research (United States) · USShizuoka Cancer Center · JPTohoku University Hospital · JP

Funding

Health Labour Sciences Special Research Grant 9EA1007
6 · The paper itself

Abstract

Comprehensive genomic profiling is increasingly used to facilitate precision oncology based on molecular stratification. In addition to conventional tissue comprehensive genomic profiling, comprehensive genomic profiling of circulating tumor DNA has become widely utilized in cancer care owing on its advantages, including less invasiveness, rapid turnaround time, and capturing heterogeneity. However, circulating tumor DNA comprehensive genomic profiling has some limitations, mainly false negatives due to low levels of plasma circulating tumor deoxyribonucleic acid and false positives caused by clonal hematopoiesis. Nevertheless, no guidelines and recommendations fully address these issues. Here, an expert panel committee involving representatives from 12 Designated Core Hospitals for Cancer Genomic Medicine in Japan was organized to develop expert consensus recommendations for the use of circulating tumor deoxyribonucleic acid-based comprehensive genomic profiling. The aim was to generate guidelines for clinicians and allied healthcare professionals on the optimal use of the circulating tumor DNA assays in advanced solid tumors and to aid the design of future clinical trials that utilize and develop circulating tumor DNA assays to refine precision oncology. Fourteen clinical questions regarding circulating tumor deoxyribonucleic acid comprehensive genomic profiling including the timing of testing and considerations for interpreting results were established by searching and curating associated literatures, and corresponding recommendations were prepared based on the literature for each clinical question. Final consensus recommendations were developed by voting to determine the level of each recommendation by the Committee members.

Indexed as

Circulating Tumor DNANeoplasmsBiomarkers, TumorDNA, NeoplasmHumansPrecision MedicineBiomarkers, TumorCirculating Tumor DNADNA, Neoplasmcirculating tumor DNAcomprehensive genomic profilingliquid biopsyprecision oncologysolid tumor

Identifiers

PMID35876224
PMCPMC9633310
OpenAlexW4287308130

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.