Evidence map›Paper›PMID 29759150›Full record

ReviewSeminars in hematology2018

Comprehensive characterization of circulating and bone marrow-derived multiple myeloma cells at minimal residual disease.

Johannes M Waldschmidt, Praveen Anand, Birgit Knoechel, Jens G Lohr

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in hematology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Capture Rate of V(D)J Sequencing for Minimal Residual Disease Detection in Multiple Myeloma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  7. Article
  8. Circulating Exosomal CircMYC Is Associated with Recurrence and Bortezomib Resistance in Patients with Multiple MyelomaTurkish journal of haematology : official journal of Turkish Society of Haematology · 2020
    Article
  9. Review
  10. Review
  11. Tracking myeloma tumor DNA in peripheral blood.Best practice & research. Clinical haematology · 2020
    Review
  12. Article
  13. Article
  14. Review
  15. Review
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

4 authors at 2 institutions in 1 country.

Johannes M WaldschmidtDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.
Praveen AnandDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA; Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.
Birgit KnoechelDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.
Jens G LohrDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA. Electronic address: jensg_lohr@dfci.harvard.edu.
Dana-Farber Cancer Institute · USHarvard University · US

Funding

Determining the mutational landscape of circulating multiple myeloma cellsK08CA191026 · NCI · DANA-FARBER CANCER INST · PI LOHR, JENS G · 2015 to 2019
$886k
Epigenetic mechanisms of drug resistance in T-cell acute lymphoblastic leukemiaK08CA191091 · NCI · DANA-FARBER CANCER INST · PI KNOECHEL, BIRGIT · 2015 to 2019
$886k
NCI NIH HHS K08 CA191026NCI NIH HHS K08 CA191091
6 · The paper itself

Abstract

The presence or absence of minimal residual disease (MRD) in patients with multiple myeloma (MM) has emerged as a useful marker to determine the depth of remission. MRD negativity as an endpoint has been shown to be associated with improved progression-free survival in many studies. MRD detection is therefore part of numerous clinical trial protocols for MM. At the present time, two methodologies are most widely accepted for MRD detection: (1) multicolor flow cytometry and (2) next-generation sequencing-based clonotype detection. While both of those methodologies enable accurate quantification of MRD in the bone marrow (BM), with sensitivity as low as 10

Indexed as

Flow CytometryHigh-Throughput Nucleotide SequencingHumansMultiple MyelomaNeoplasm, ResidualPrognosisCirculating multiple myeloma cellsClonal evolutionMRDNext-generation sequencing

Identifiers

PMID29759150
PMCPMC6145140
OpenAlexW2790141674

What OpenQuestion holds

Textmetadata
LicenceTDM
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.