Evidence map›Paper›PMID 22102709›Full record

Trial reportHaematologica2012

Detection of minimal residual disease following induction immunochemotherapy predicts progression free survival in mantle cell lymphoma: final results of CALGB 59909.

Hongtao Liu, Jeffrey L Johnson, Greg Koval, Greg Malnassy, Dorie Sher, Lloyd E Damon, Eric D Hsi, Donna Marie Bucci, Charles A Linker, Bruce D Cheson and 1 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Haematologica, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 77 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Review
  7. Article
  8. What is the role of up-front autologous stem cell transplantation in mantle cell lymphoma?Hematology. American Society of Hematology. Education Program · 2022
    Article
  9. Review
  10. Targeting Refractory Mantle Cell Lymphoma for Imaging and Therapy Using C-X-C Chemokine Receptor Type 4 Radioligands.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  11. Hematopoietic cell transplantation for mantle cell lymphoma.International journal of hematology · 2022
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Minimal Residual Disease Assessment in Lymphoma: Methods and Applications.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2017
    Review
  18. Article
  19. Review
  20. Recommendations for Clinical Trial Development in Mantle Cell Lymphoma.Journal of the National Cancer Institute · 2017
    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

11 authors at 7 institutions in 1 country.

Hongtao LiuUniversity of Chicago Medical Center 5841, S. Maryland Ave, MC2115 Chicago, IL 60637, USA.
Jeffrey L Johnson
Greg Koval
Greg Malnassy
Dorie Sher
Lloyd E Damon
Eric D Hsi
Donna Marie Bucci
Charles A Linker
Bruce D Cheson
Wendy Stock
University of Chicago Medical Center · USCleveland Clinic · USDuke University Hospital · USGeorgetown University · USThe Ohio State University · USUniversity of California, San Francisco · USUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn the present study, the prognostic impact of minimal residual disease during treatment on time to progression and overall survival was analyzed prospectively in patients with mantle cell lymphoma treated on the Cancer and Leukemia Group B 59909 clinical trial. DESIGN AND

methodsPeripheral blood and bone marrow samples were collected during different phases of the Cancer and Leukemia Group B 59909 study for minimal residual disease analysis. Minimal residual disease status was determined by quantitative polymerase chain reaction of IgH and/or BCL-1/JH gene rearrangement. Correlation of minimal residual disease status with time to progression and overall survival was determined. In multivariable analysis, minimal residual disease, and other risk factors were correlated with time to progression.

resultsThirty-nine patients had evaluable, sequential peripheral blood and bone marrow samples for minimal residual disease analysis. Using peripheral blood monitoring, 18 of 39 (46%) achieved molecular remission following induction therapy. The molecular remission rate increased from 46 to 74% after one course of intensification therapy. Twelve of 21 minimal residual disease positive patients (57%) progressed within three years of follow up compared to 4 of 18 (22%) molecular remission patients (P=0.049). Detection of minimal residual disease following induction therapy predicted disease progression with a hazard ratio of 3.7 (P=0.016). The 3-year probability of time to progression among those who were in molecular remission after induction chemotherapy was 82% compared to 48% in patients with detectable minimal residual disease. The prediction of time to progression by post-induction minimal residual disease was independent of other prognostic factors in multivariable analysis.

conclusionsDetection of minimal residual disease following induction immunochemotherapy was an independent predictor of time to progression following immunochemotherapy and autologous stem cell transplantation for mantle cell lymphoma.

Indexed as

ImmunotherapyInduction ChemotherapyAdultAgedAntineoplastic Combined Chemotherapy ProtocolsHematopoietic Stem Cell TransplantationHumansLymphoma, Mantle-CellMiddle AgedNeoplasm, ResidualPrognosisSurvival AnalysisTransplantation, AutologousTreatment Outcome

Identifiers

PMID22102709
PMCPMC3347669
OpenAlexW2131956233

What OpenQuestion holds

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Registered trials

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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.