Evidence map›Paper›PMID 39372864›Full record

ArticleFrontiers in oncology2024

Utilization of tissue-free minimal residual disease testing in colorectal cancer patients from Asia and Middle East.

Suyog Jain, Shaheenah Dawood, Viraj Lavingia, Dan Aderka, Esther Tahover, Yao-Yu Hsieh, Mark Temper, Alesya Goldman, Marwan Ai Akasheh, Steve Olsen and 3 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Observational
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

13 authors.

Suyog JainMedical Affairs Department, Guardant Health Pte Ltd, Singapore, Singapore.
Shaheenah DawoodDepartment of Medical Oncology, Mediclinic City Hospital, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Viraj LavingiaDepartment of Medical Oncology, Shalby Hospital, Ahmedabad, India.
Dan AderkaOncology Department, Assuta Ramat Hahayal, Tel Aviv-Yafo, Israel.
Esther TahoverOncology Department, Assuta Ramat Hahayal, Tel Aviv-Yafo, Israel.
Yao-Yu HsiehDivision of Hematology and Oncology, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
Mark TemperCenter of Oncology, Hadassah University Medical Center, Jerusalem, Israel.
Alesya GoldmanOncology Department, Meir Medical Center, Kfar-Saba, Israel.
Marwan Ai AkashehDepartment of Oncology, Maggi Medical Centre, Amman, Jordan.
Steve OlsenMedical Affairs Department, Guardant Health Pte Ltd, Singapore, Singapore.
Sandra San HsingMedical Affairs Department, Guardant Health Pte Ltd, Singapore, Singapore.
Nisarg JoshiMedical Affairs Department, Guardant Health Pte Ltd, Singapore, Singapore.
Hsiao-Yu JenMedical Affairs Department, Guardant Health Pte Ltd, Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The presence of minimal residual disease (MRD) after curative-intent surgery for early-stage cancers is associated with disease recurrence. Circulating tumour deoxyribonucleic acid (ctDNA) has emerged as a promising biomarker for MRD assessment in patients with colorectal cancer (CRC) who have undergone surgery or completed adjuvant therapy. MRD tests are already available for use in clinics; however, treatment decisions following MRD results obtained in routine practice are infrequently described. Methods: In this observational study, we report on the real-world clinical use of Guardant Reveal, a validated tissue-free MRD assay, in the first 215 consecutive patients (279 samples) with CRC tested in Asia and the Middle East. Results: Overall, 22% of patients had ctDNA detected in their first MRD test, and the frequency of ctDNA positivity increased with increasing tumour stage. 132 samples were tested with an earlier version of Guardant Reveal, one that assessed both genomic and epigenomic features. An updated version of the assay assesses only ctDNA methylation data and was used for the remaining 147 samples. In patients with stage II CRC, 71% of tests were ordered within 12 weeks after tumour resection, while for patients with stage III disease, 69% of tests were ordered after completion of all curative-intent treatment. Discussion: Clinical cases utilizing tissue-free MRD assessment are described.

Indexed as

CRC - colorectal cancerctDNA - circulating tumour DNAepigenomicsliquid biopsymethylationMRD - molecular residual diseaseReveal

Identifiers

PMID39372864
PMCPMC11449681

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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.