Evidence map›Paper›PMID 35992818›Full record

ReviewFrontiers in oncology2022

Allogeneic Hematopoietic Stem Cell Transplantation for Mixed or Overlap Myelodysplastic/Myeloproliferative Disorders.

Argiris Symeonidis, Spiros Chondropoulos, Evgenia Verigou, Vasileios Lazaris, Alexandra Kourakli, Panagiotis Tsirigotis

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Successful Allogeneic Stem Cell Transplantation with Ruxolitinib Maintenance Therapy forTurkish journal of haematology : official journal of Turkish Society of Haematology · 2023
    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

6 authors at 4 institutions in 1 country.

Argiris SymeonidisUniversity of Patras Medical School, Hematology Division, Patras, Greece.
Spiros ChondropoulosUniversity General Hospital Attikon, Athens, Greece.
Evgenia VerigouHematology Division, General University Hospital of Patras, Rion of Patras, Greece.
Vasileios LazarisHematology Division, General University Hospital of Patras, Rion of Patras, Greece.
Alexandra KourakliHematology Division, General University Hospital of Patras, Rion of Patras, Greece.
Panagiotis TsirigotisDepartment of Medicine, School of Health Sciences, National and Kapodistrian University of Athens, Athens, Greece.
General University Hospital of Patras · GRNational and Kapodistrian University of Athens · GRUniversity General Hospital Attikon · GRUniversity of Patras · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic myelomonocytic leukemia (CMML) and the remaining, less frequent hybrid, mixed, or overlap myelodysplastic syndromes/myeloproliferative neoplasms (MDSs/MPNs) are difficult to treat neoplastic hematological disorders, exhibiting substantial clinical and prognostic heterogeneity, for which clear therapeutic guidelines or effective treatment options are still missing. CMML has an overall survival ranging from a few months to several years. Although patients with proliferative or dysplastic features may benefit from hydroxyurea and hypomethylating agent treatment, respectively, none of these treatments can establish long-term remission and prevent the inevitable transformation to acute leukemia. Novel targeted treatment approaches are emerging but are still under investigation. Therefore, currently, allogeneic stem cell transplantation (allo-SCT) remains the only treatment modality with a curative potential, but its widespread application is limited, due to significant morbidity and mortality associated with the procedure, especially in the elderly and in patients with comorbidities. Recognition of patient eligibility for allo-SCT is crucial, and the procedure should be addressed to patients with a good performance status without severe comorbidities and mainly to those in intermediate- to high-risk category, with a suitable stem cell donor available. The issues of best timing for performing transplantation, patient and donor eligibility, the type of conditioning regimen, and the outcomes after various allo-SCT procedures are the topics of this review.

Indexed as

allogeneic stem cell transplantationatypical chronic myelogenous leukemia (aCML)chronic myelomonocytic leukemia (CMML)chronic neutrophilic leukemia (CNL)Juvenile Myelomonocytic Leukemia (JMML)outcomeprognosis

Identifiers

PMID35992818
PMCPMC9389581
OpenAlexW4289933116

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.