Evidence map›Paper›PMID 15538405›Full record

Trial reportLeukemia2005

Drug-induced immunophenotypic modulation in childhood ALL: implications for minimal residual disease detection.

G Gaipa, G Basso, O Maglia, V Leoni, A Faini, G Cazzaniga, C Bugarin, M Veltroni, B Michelotto, R Ratei and 5 more

Registry-linked trialOpen access · greenAbstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Leukemia, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01429610 (Phase 2 Study Evaluating the Efficacy of Rituximab Plus Modified VPDL for Newly Diagnosed CD20-Positive Adult Acute Lymphoblastic Leukemia), which is not on this map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
5.3field-weighted citation impact, top 5% 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.

NCT01429610 phase2unknown statusnot on this mapstarted 2011, after this paper: background citation

Phase 2 Study Evaluating the Efficacy of Rituximab Plus Modified VPDL for Newly Diagnosed CD20-Positive Adult Acute Lymphoblastic Leukemia

TypeinterventionalSponsorAsan Medical CenterRan2011 to 2019Enrolled78ConditionsPrecursor Cell Lymphoblastic Leukemia-LymphomaArmsRituximab+mVPDL
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 144 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Observational
  5. Review
  6. Article
  7. Advances in laboratory medicine · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Flow Cytometric Minimal Residual Disease Analysis in Acute Leukemia: Current Status.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2020
    Review
  14. Review
  15. Novel Therapies in Acute Lymphoblastic Leukemia.Current hematologic malignancy reports · 2018
    Review
  16. Article
  17. Review
  18. Minimal Residual Disease Detection and EvolvedFrontiers in immunology · 2016
    Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 3 countries.

G GaipaCentro Ricerca M Tettamanti, Clinica Pediatrica Università Milano-Bicocca, Ospedale San Gerardo, Via Donizetti 106, 20052 Monza, Milan, Italy.
G Basso
O Maglia
V Leoni
A Faini
G Cazzaniga
C Bugarin
M Veltroni
B Michelotto
R Ratei
T Coliva
M G Valsecchi
A Biondi
M N Dworzak
I-BFM-ALL-FCM-MRD Study Group
University of Milano-Bicocca · ITUniversity of Padua · ITCharité - Universitätsmedizin Berlin · DESt Anna Children's Hospital · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Assessment of minimal residual disease (MRD) by flow cytometry is considered to be based on the reproducibility of the leukemic immunophenotype detected at diagnosis. However, we previously noticed modulation of surface antigen expression in acute lymphoblastic leukemia (ALL) during the early treatment. Hence, we investigated this in 30 children with B-cell precursor ALL consecutively enrolled in the AIEOP-BFM ALL 2000 protocol. Quantitative expression of seven antigens useful in MRD monitoring was studied at diagnosis and compared to that measured at different time points of remission induction therapy. Downmodulation in the expression of CD10 and CD34 occurred at follow-up. By contrast, upmodulation of CD19, CD20, CD45RA, and CD11a was observed, while the expression of CD58 remained stable. Despite this, we could unambiguously discriminate leukemic cells from normal residual B cells. This holds true when bone marrow (BM) samples from similarly treated T-ALL patients, but not from healthy donors, were used as reference. Our results indicate that immunophenotypic modulation occurs in ALL during the early phases of BFM-type protocols. However, the accuracy of MRD detection by flow cytometry seems not negatively affected if adequate analysis protocols are employed. Investigators should take this phenomenon into account in order to avoid pitfalls in flow cytometric MRD studies.

Indexed as

Neoplasm, ResidualAntigens, CDChildCohort StudiesHumansImmunophenotypingPolymerase Chain ReactionPrecursor Cell Lymphoblastic Leukemia-LymphomaRemission InductionAntigens, CD

Identifiers

PMID15538405
OpenAlexW2002352053

What OpenQuestion holds

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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.