Evidence map›Paper›PMID 30878316›Full record

ArticleClinical lymphoma, myeloma & leukemia2019

Immune Signatures Associated With Clonal Isotype Switch After Autologous Stem Cell Transplantation for Multiple Myeloma.

Rebecca Ye, Sirisha Kundrapu, Stanton L Gerson, James J Driscoll, Rose Beck, Naveed Ali, Ola Landgren, Willem VanHeeckeren, George Luo, Nicolaus Kroger and 3 more

Open access · greenAbstract read
In one paragraph

Article in Clinical lymphoma, myeloma & leukemia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  5. Article
  6. The burden of myeloma: novel approaches to disease assessment.Hematology. American Society of Hematology. Education Program · 2022
    Review
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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

13 authors at 8 institutions in 2 countries.

Rebecca YeDepartment of Medicine, New York University School of Medicine, New York, NY.
Sirisha KundrapuDepartment of Pathology, University Hospitals Cleveland Medical Center, Cleveland, OH.
Stanton L GersonCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH.
James J DriscollDivision of Hematology and Oncology, The Vontz Center for Molecular Studies, University of Cincinnati College of Medicine, Cincinnati, OH.
Rose BeckDepartment of Pathology, University Hospitals Cleveland Medical Center, Cleveland, OH.
Naveed AliAdult Hematologic Malignancies and Stem Cell Transplant Program, Seidman Cancer Center, University Hospitals Cleveland Medical Center, Cleveland, OH.
Ola LandgrenMyeloma Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY.
Willem VanHeeckerenDivision of Hematology and Oncology, University Hospital Cleveland Medical Center, Cleveland, OH.
George LuoCase Western Reserve University School of Medicine, Cleveland, OH.
Nicolaus KrogerDepartment of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Paolo CaimiAdult Hematologic Malignancies and Stem Cell Transplant Program, Seidman Cancer Center, University Hospitals Cleveland Medical Center, Cleveland, OH; Case Western Reserve University School of Medicine, Cleveland, OH.
Marcos De LimaAdult Hematologic Malignancies and Stem Cell Transplant Program, Seidman Cancer Center, University Hospitals Cleveland Medical Center, Cleveland, OH; Case Western Reserve University School of Medicine, Cleveland, OH.
Ehsan MalekAdult Hematologic Malignancies and Stem Cell Transplant Program, Seidman Cancer Center, University Hospitals Cleveland Medical Center, Cleveland, OH; Case Western Reserve University School of Medicine, Cleveland, OH. Electronic address: exm301@case.edu.
University Hospitals Seidman Cancer Center · USUniversity Hospitals of Cleveland · USCase Western Reserve University · USMemorial Sloan Kettering Cancer Center · USNew York University · USUniversität Hamburg · DEUniversity of Cincinnati Medical Center · USUniversity School · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundHigh-dose chemotherapy and autologous stem cell transplantation (ASCT) are integral components of the overall treatment for patients with multiple myeloma (MM) aged ≤ 65 years. The emergence of oligoclonal immunoglobulin bands (ie, immunoglobulins differing from those originally identified at diagnosis [termed clonal isotype switch (CIS)]) has been reported in patients with MM after high-dose chemotherapy followed by autologous stem cell transplantation. However, the clinical relevance and the correlation with immune reconstitution remains unclear. PATIENTS AND

methodsPatients with MM who had undergone ASCT from 2007 to 2016 were included in the present study. The percentage of natural killer cells, B-cells, and T-cells was measured using flow cytometry in pre- and post-ASCT bone marrow samples. CIS was defined as the appearance of a new serum monoclonal spike on serum protein electrophoresis and immunofixation that differed from original heavy or light chain detected at diagnosis.

resultsA retrospective analysis of 177 patients with MM who had undergone ASCT detected CIS in 39 (22%). CIS after ASCT correlated with improved progression-free survival (52.2 vs. 36.6 months; P = .21) and overall survival (75.1 vs. 65.4 months; P = .021). Patients with a relapse had an isotype that differed from a CIS, confirming the benign nature of this phenomenon. CIS was also associated with lower CD8 T-cell percentages and a greater CD4/CD8 ratio (2.8 vs. 0.2; P = .001) compared with patients who did not demonstrate a CIS, suggestive of more profound T-cell immune reconstitution in this group.

conclusionTaken together, our data have demonstrated that a CIS is a benign phenomenon and correlates with a reduced disease burden and enriched immune repertoire beyond the B-cell compartment.

Indexed as

Hematopoietic Stem Cell TransplantationAdultAgedB-LymphocytesDose-Response Relationship, DrugFemaleHumansImmune ReconstitutionImmunoglobulin Class SwitchingImmunoglobulin IsotypesMaleMiddle AgedMultiple MyelomaMyeloablative AgonistsPostoperative PeriodPrognosisImmunoglobulin IsotypesMyeloablative AgonistsAutologous stem cell transplantationClonal isotype switchImmune reconstitutionMultiple myelomaMyeloma microenvironment

Identifiers

PMID30878316
PMCPMC7444684
OpenAlexW2907632637

What OpenQuestion holds

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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.