Evidence map›Paper›PMID 27711974›Full record

Trial reportBritish journal of haematology2016

Next-generation sequencing-based detection of circulating tumour DNA After allogeneic stem cell transplantation for lymphoma.

Alex F Herrera, Haesook T Kim, Katherine A Kong, Malek Faham, Heather Sun, Aliyah R Sohani, Edwin P Alyea, Victoria E Carlton, Yi-Bin Chen, Corey S Cutler and 9 more

Abstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in British journal of haematology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 3 pooled it
–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

34 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Review
  7. Liquid Biopsy in B and T Cell Lymphomas: From Bench to Bedside.International journal of molecular sciences · 2025
    Review
  8. Article
  9. Review
  10. Article
  11. B-cell non-Hodgkin lymphomas.Lancet (London, England) · 2024
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Stance of MRD in Non-Hodgkin's Lymphoma and its upsurge in the novel era of cell-free DNA.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
    Review
  17. Review
  18. Article
  19. Article
  20. Measurable residual disease in the treatment of chronic lymphocytic leukemia.Journal of clinical and experimental hematopathology : JCEH · 2020
    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

19 authors.

Alex F HerreraDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA, USA.
Haesook T KimDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
Katherine A KongAdaptive Biotechnologies Corp., South San Francisco, CA, USA.
Malek FahamAdaptive Biotechnologies Corp., South San Francisco, CA, USA.
Heather SunDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Aliyah R SohaniDepartment of Pathology, Massachusetts General Hospital, Boston, MA, USA.
Edwin P AlyeaDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
Victoria E CarltonAdaptive Biotechnologies Corp., South San Francisco, CA, USA.
Yi-Bin ChenDivision of Bone Marrow Transplantation, Massachusetts General Hospital, Boston, MA, USA.
Corey S CutlerDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
Vincent T HoDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
John KorethDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
Chitra KotwaliwaleAdaptive Biotechnologies Corp., South San Francisco, CA, USA.
Sarah NikiforowDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
Jerome RitzDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
Scott J RodigDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Robert J SoifferDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
Joseph H AntinDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.
Philippe ArmandDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA, USA.

Funding

Project 3: Humoral Targets and B Cell Biology in Chronic Graft-vs.-Host DiseaseP01CA142106 · NCI · DANA-FARBER CANCER INST · PI CUTLER, COREY S · 2009 to 2019
$17.5M
Oncology Research Career Development ProgramK12CA001727 · NCI · CITY OF HOPE NATIONAL MEDICAL CENTER · PI MORTIMER, JOANNE E. · 1992 to 2024
$14.6M
Targeting SYK Kinase in AMLP50CA206963 · NCI · DANA-FARBER CANCER INST · PI ASTER, JON C. · 2017 to 2021
$10.6M
Manipulation of Immune Responsiveness after Hematopoietic Cell TransplantationR01CA183559 · NCI · DANA-FARBER CANCER INST · PI RITZ, JEROME, SOIFFER, ROBERT JON · 2013 to 2017
$3.7M
Reconstitution of Regulatory T Cells After Stem Cell TransplantationR01CA183560 · NCI · DANA-FARBER CANCER INST · PI RITZ, JEROME, SOIFFER, ROBERT JON · 2013 to 2017
$2.5M
NCI NIH HHS K12 CA001727NCI NIH HHS P01 CA142106NCI NIH HHS P50 CA206963NCI NIH HHS R01 CA183559NCI NIH HHS R01 CA183560
6 · The paper itself

Abstract

Next-generation sequencing (NGS)-based circulating tumour DNA (ctDNA) detection is a promising monitoring tool for lymphoid malignancies. We evaluated whether the presence of ctDNA was associated with outcome after allogeneic haematopoietic stem cell transplantation (HSCT) in lymphoma patients. We studied 88 patients drawn from a phase 3 clinical trial of reduced-intensity conditioning HSCT in lymphoma. Conventional restaging and collection of peripheral blood samples occurred at pre-specified time points before and after HSCT and were assayed for ctDNA by sequencing of the immunoglobulin or T-cell receptor genes. Tumour clonotypes were identified in 87% of patients with adequate tumour samples. Sixteen of 19 (84%) patients with disease progression after HSCT had detectable ctDNA prior to progression at a median of 3·7 months prior to relapse/progression. Patients with detectable ctDNA 3 months after HSCT had inferior progression-free survival (PFS) (2-year PFS 58% vs. 84% in ctDNA-negative patients, P = 0·033). In multivariate models, detectable ctDNA was associated with increased risk of progression/death (Hazard ratio 3·9, P = 0·003) and increased risk of relapse/progression (Hazard ratio 10·8, P = 0·0006). Detectable ctDNA is associated with an increased risk of relapse/progression, but further validation studies are necessary to confirm these findings and determine the clinical utility of NGS-based minimal residual disease monitoring in lymphoma patients after HSCT.

Indexed as

AdolescentAdultAgedDeathDisease ProgressionDNA, NeoplasmFemaleHematopoietic Stem Cell TransplantationHumansImmunoglobulinsLymphomaMaleMiddle AgedNeoplasm, ResidualReceptors, Antigen, T-CellRecurrenceDNA, NeoplasmImmunoglobulinsReceptors, Antigen, T-Cellchronic lymphocytic leukaemialymphomasminimal residual diseasenon-Hodgkin lymphomastem cell transplantation

Identifiers

PMID27711974
PMCPMC5123935

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.