Evidence map›Paper›PMID 35496349›Full record

ArticlePharmacogenomics and personalized medicine2022

Therapeutic Management of Patients with FLT3 + Acute Myeloid Leukemia: Case Reports and Focus on Gilteritinib Monotherapy.

Monica Bocchia, Angelo Michele Carella, Antonino Mulè, Lorenzo Rizzo, Mauro Turrini, Maria Chiara Abbenante, Roberto Cairoli, Valeria Calafiore, Marzia Defina, Angelo Gardellini and 7 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Pharmacogenomics and personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
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

17 authors at 6 institutions in 1 country.

Monica BocchiaHematology Unit, Azienda Ospedaliera Universitaria Senese, University of Siena, Siena, Italy.
Angelo Michele CarellaDivision of Hematology with Hematologic Intensive Care Unit and Cellular Therapies, Department of Medical Science, Fondazione IRCCS Casa Sollievo Della Sofferenza, Foggia, Italy.
Antonino MulèUOC Hematology and Oncology, Ospedali Riuniti Villa Sofia-Cervello, Palermo, Italy.
Lorenzo RizzoDepartment of Haematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
Mauro TurriniDivision of Hematology, Valduce Hospital, Como, Italy.
Maria Chiara AbbenanteDivision of Hematology with Hematologic Intensive Care Unit and Cellular Therapies, Department of Medical Science, Fondazione IRCCS Casa Sollievo Della Sofferenza, Foggia, Italy.
Roberto CairoliDepartment of Haematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
Valeria CalafioreUOC Hematology and Oncology, Ospedali Riuniti Villa Sofia-Cervello, Palermo, Italy.
Marzia DefinaHematology Unit, Azienda Ospedaliera Universitaria Senese, University of Siena, Siena, Italy.
Angelo GardelliniDivision of Hematology, Valduce Hospital, Como, Italy.
Giovanni LuziUOC Hematology and Stem Cell Transplant Unit, Ospedale S, Camillo, Rome, Italy.
Caterina PattiUOC Hematology and Oncology, Ospedali Riuniti Villa Sofia-Cervello, Palermo, Italy.
Maria Beatrice PinazziUOC Hematology and Stem Cell Transplant Unit, Ospedale S, Camillo, Rome, Italy.
Marta RivaDepartment of Haematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
Giovanni RossiDivision of Hematology with Hematologic Intensive Care Unit and Cellular Therapies, Department of Medical Science, Fondazione IRCCS Casa Sollievo Della Sofferenza, Foggia, Italy.
Vincenzo SammartanoHematology Unit, Azienda Ospedaliera Universitaria Senese, University of Siena, Siena, Italy.
Luigi RigacciUOC Hematology and Stem Cell Transplant Unit, Ospedale S, Camillo, Rome, Italy.
Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda · ITCasa Sollievo della Sofferenza · ITOspedale Vincenzo Cervello · ITOspedale Valduce · ITUniversity of Siena · ITAzienda Ospedaliera Universitaria Senese · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia is a malignant disorder of the bone marrow, characterized by differentiation, clonal expansion, and uncontrolled proliferation of malignant myeloid progenitor cells and by several molecular and genetic abnormalities. A mutation of FMS-like tyrosine kinase 3 gene can be observed in about one-third of cases of acute myeloid leukemia. Two FLT3 inhibitors are actually approved for FLT3 mutated acute myeloid leukemia: midostaurin, a multikinase first generation inhibitor with lower affinity for FLT3 binding, and gilteritinib fumarate, a potent second-generation inhibitor of both FLT3-ITD and TKD. Gilteritinib is a new effective and well-tolerated drug for patients with relapsing or refractory FLT3-positive acute myeloid leukemia. Thanks to its efficacy, low toxicity, its good manageability (oral formulation), this drug is suitable for all the patients, including elderly frail patient with concomitant therapies or pre-existing or underlying diseases, and can be used also in the outpatient setting, reducing risks and costs related to the hospitalization. We report and discuss seven cases of different patients with FLT3 positive acute myeloid leukemia successfully managed with gilteritinib in the real clinical practice.

Indexed as

acute myeloid leukemiaFLT3gilteritinibmidostaurin

Identifiers

PMID35496349
PMCPMC9041600
OpenAlexW4224305243

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

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.