Evidence map›Paper›PMID 34661826›Full record

ArticleTargeted oncology2021

Making Treatment-Free Remission (TFR) Easier in Chronic Myeloid Leukemia: Fact-Checking and Practical Management Tools.

Fausto Castagnetti, Gianni Binotto, Isabella Capodanno, Atto Billio, Elisabetta Calistri, Francesco Cavazzini, Monica Crugnola, Antonella Gozzini, Gabriele Gugliotta, Mauro Krampera and 12 more

Abstract read
In one paragraph

Article in Targeted oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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.

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

7 citing papers in PubMed.

  1. Trial
  2. Article
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  5. Review
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  7. 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.

Fausto CastagnettiIstituto di Ematologia "Seràgnoli", IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy. fausto.castagnetti@unibo.it.
Gianni BinottoHematology and Clinical Immunology Unit, University of Padua, Padua, Italy.
Isabella CapodannoHematology Unit, Azienda Unità Sanitaria Locale-IRCCS, Reggio Emilia, Italy.
Atto BillioHematology and Bone Marrow Transplantation, Ospedale di Bolzano, Bolzano, Italy.
Elisabetta CalistriOspedale di Treviso, Treviso, Italy.
Francesco CavazziniHematology Unit, Azienda Ospedaliero-Universitaria "S.Anna", Ferrara, Italy.
Monica CrugnolaHematology Unit and BMT, Azienda Ospedaliero Universitaria, Parma, Italy.
Antonella GozziniDepartment of Cellular Therapies and Transfusion Medicine, Azienda Ospedaliero-Universitaria Careggi, Florence, Italy.
Gabriele GugliottaIstituto di Ematologia "Seràgnoli", IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Mauro KramperaSection of Hematology and Bone Marrow Transplant Unit, Department of Medicine, University of Verona, Verona, Italy.
Alessandro LucchesiHematology Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Anna MerliHematology Unit, Ospedale Infermi Rimini, AUSL Romagna, Rimini, Italy.
Maria Cristina MiggianoHematology Department, San Bortolo Hospital, Vicenza, Italy.
Claudia MinottoMedical Oncology and Onco-Hematology Unit, AULSS 3 Serenissima distretto di Dolo-Mirano, Venice, Italy.
Monica PoggiaspallaHematology Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Marzia SalvucciHematology Unit, Oncology and Hematology Department, Ospedale Civico, Ravenna, Italy.
Barbara ScappiniHematology Unit, Azienda Ospedaliero-Universitaria Careggi, Florence, Italy.
Mario TiribelliDivision of Hematology and BMT, Department of Medical Area, University of Udine, Udine, Italy.
Elena TrabacchiHematology Unit and BMT Center, Ospedale G. Saliceto, Piacenza, Italy.
Gianantonio RostiScientific Direction, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, FC, Italy.
Sara GalimbertiSection of Hematology, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Massimiliano BonifacioSection of Hematology and Bone Marrow Transplant Unit, Department of Medicine, University of Verona, Verona, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In chronic-phase chronic myeloid leukemia (CML), tyrosine kinase inhibitors (TKIs) are the standard of care, and treatment-free remission (TFR) following the achievement of a stable deep molecular response (DMR) has become, alongside survival, a primary goal for virtually all patients. The GIMEMA CML working party recently suggested that the possibility of achieving TFR cannot be denied to any patient, and proposed specific treatment policies according to the patient's age and risk. However, other international recommendations (including 2020 ELN recommendations) are more focused on survival and provide less detailed suggestions on how to choose first and subsequent lines of treatment. Consequently, some grey areas remain. After literature review, a panel of Italian experts discussed the following controversial issues: (1) early prediction of DMR and TFR: female sex, non-high disease risk score, e14a2 transcript and early MR achievement have been associated with stable DMR, but the lack of these criteria is not sufficient to exclude any patient from TFR; (2) criteria for first and subsequent line therapy choice: a number of patient and drug characteristics have been proposed to make a personalized decision; (3) monitoring of residual disease after discontinuation: after the first 6 months, the frequency of molecular tests can be reduced based on MR4.5 persistence and short turnaround time; (4) prognosis of TFR: therapy and DMR duration are important to predict TFR; although immunological control of CML plays a role, no immunological predictive phenotype is currently available. This guidance is intended as a practical tool to support physicians in decision making.

Indexed as

Leukemia, Myelogenous, Chronic, BCR-ABL PositiveProtein Kinase InhibitorsFemaleHumansPrognosisRemission InductionTreatment OutcomeProtein Kinase Inhibitors

Identifiers

PMID34661826
PMCPMC8613078

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.