Evidence map›Paper›PMID 33558202›Full record

ArticleClinical lymphoma, myeloma & leukemia2021

Noninvasive Monitoring of Mantle Cell Lymphoma by Immunoglobulin Gene Next-Generation Sequencing in a Phase 2 Study of Sequential Chemoradioimmunotherapy Followed by Autologous Stem-Cell Rescue.

Anita Kumar, K S Bantilan, A P Jacob, A Park, S F Schoninger, C Sauter, G A Ulaner, C Casulo, M Faham, K A Kong and 12 more

Registry-linked trialAbstract read
In one paragraph

Article in Clinical lymphoma, myeloma & leukemia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01484093 (Sequential Chemo-Radioimmunotherapy Followed by Autologous Transplantation for Patients With Untreated Advanced Stage Mantle Cell Lymphoma), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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.

NCT01484093 phase1 / phase2completednot on this map

Sequential Chemo-Radioimmunotherapy Followed by Autologous Transplantation for Patients With Untreated Advanced Stage Mantle Cell Lymphoma: A Phase I/II Trial

TypeinterventionalSponsorMemorial Sloan Kettering Cancer CenterRan2011 to 2023Enrolled96ConditionsMantle Cell LymphomaArmsR-CHOP-14R-HIDAC,followed by RIT/HDT/ASCR.
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
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  6. 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

22 authors.

Anita KumarDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY. Electronic address: kumara2@mskcc.org.
K S BantilanDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
A P JacobAdaptive Biotechnologies, Seattle, WA.
A ParkDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
S F SchoningerDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
C SauterDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
G A UlanerDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
C CasuloDepartment of Medicine, Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY.
M FahamAdaptive Biotechnologies, Seattle, WA.
K A KongAdaptive Biotechnologies, Seattle, WA.
R K GrewalDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
J GerecitanoDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
A HamiltonDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
P HamlinDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
M MatasarDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
C H MoskowitzDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
A NoyDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
M L PalombaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
C S PortlockDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
A YounesDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
T WillisAdaptive Biotechnologies, Seattle, WA.
A D ZelenetzDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

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

backgroundMinimal residual disease (MRD) monitoring has been used to identify early molecular relapse and predict clinical relapse in mantle cell lymphoma (MCL). Few published data exist in MCL on the performance of next-generation sequencing-based assay of immunoglobulin gene rearrangements for MRD assessment. PATIENTS AND

methodsIn a prospective clinical trial (NCT01484093) with intensive induction chemotherapy and autologous stem-cell transplantation, posttreatment peripheral blood samples were collected from 16 MCL patients and analyzed with an earlier version of the Adaptive Biotechnologies MRD assay.

resultsOf the 7 patients whose disease remained in remission, the MRD test remained negative in 5 (71%). Of the 9 patients who experienced relapse, the MRD test was positive at least 3 months before relapse in 6 patients (67%) and positive at the time of relapse in 1 patient (11%). All patients with at least 2 positive MRD tests experienced relapse.

conclusionThe next-generation sequencing-based MRD assay identified early molecular relapse, and we observed more sensitivity in the cellular (circulating leukocytes) versus acellular (plasma cell-free DNA) compartment. This observation may be due to availability of tumor target or a limitation of the assay.

Indexed as

AgedChemoradiotherapyDNA, NeoplasmFemaleGene RearrangementHigh-Throughput Nucleotide SequencingHumansImmunoglobulinsImmunotherapyInduction ChemotherapyLymphoma, Mantle-CellMaleMiddle AgedNeoplasm Recurrence, LocalNeoplasm, ResidualNeoplastic Cells, CirculatingDNA, NeoplasmImmunoglobulinsHigh-dose therapyMinimal residual diseaseSurveillance

Identifiers

PMID33558202
PMCPMC9476895

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Registered trials

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.