Evidence map›Paper›PMID 36570691›Full record

ArticleHemaSphere2023

Machine Learning Improves Risk Stratification in Myelofibrosis: An Analysis of the Spanish Registry of Myelofibrosis.

Adrián Mosquera-Orgueira, Manuel Pérez-Encinas, Alberto Hernández-Sánchez, Teresa González-Martínez, Eduardo Arellano-Rodrigo, Javier Martínez-Elicegui, Ángela Villaverde-Ramiro, José-María Raya, Rosa Ayala, Francisca Ferrer-Marín and 22 more

Open access · goldAbstract read
In one paragraph

Article in HemaSphere, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. 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

32 authors at 20 institutions in 3 countries.

Adrián Mosquera-OrgueiraHospital Clínico Universitario, Santiago de Compostela, Spain.
Manuel Pérez-EncinasHospital Clínico Universitario, Santiago de Compostela, Spain.
Alberto Hernández-SánchezHospital Clínico, Salamanca, Spain.
Teresa González-MartínezHospital Clínico, Salamanca, Spain.
Eduardo Arellano-RodrigoHospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.
Javier Martínez-EliceguiHospital Clínico, Salamanca, Spain.
Ángela Villaverde-RamiroHospital Clínico, Salamanca, Spain.
José-María RayaHospital Universitario de Canarias, Tenerife, Spain.
Rosa AyalaHospital Universitario 12 de Octubre, Madrid, Spain.
Francisca Ferrer-MarínHospital Morales Meseguer, Universidad Católica San Antonio de Murcia, Centro de Investigación Biomédica en Red de Enfermedades Raras, Murcia, Spain.
María-Laura FoxVall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Spain.
Patricia VelezHospital del Mar, Barcelona, Spain.
Elvira MoraHospital Universitario La Fe, Valencia, Spain.
Blanca XicoyHospital Germans Trias i Pujol, Institut Català d'Oncologia, Josep Carreras Leukemia Research Institute, Universitat Autònoma de Barcelona, Badalona, Spain.
María-Isabel Mata-VázquezHospital Costa del Sol, Marbella, Spain.
María García-FortesHospital Virgen de la Victoria, Málaga, Spain.
Anna AngonaHospital Josep Trueta, Institut Catalá d'Oncologia, Girona, Spain.
Beatriz CuevasHospital Universitario de Burgos, Burgos, Spain.
María-Alicia SenínInstitut Catalá d'Oncologia, L'Hospitalet de Llobregat, Spain.
Angel Ramírez-PayerHospital Universitario Central de Asturias, Oviedo, Spain.
María-José RamírezHospital General, Jerez de la Frontera, Spain.
Raúl Pérez-LópezHospital Virgen de la Arrixaca, Murcia, Spain.
Sonia González de VillambrosíaHospital Marqués de Valdecilla, Santander, Spain.
Clara Martínez-ValverdeHospital de la Santa Creu i Sant Pau, Barcelona, Spain.
María-Teresa Gómez-CasaresHospital Dr Negrín, Las Palmas de Gran Canaria, Spain.
Carmen García-HernándezHospital General, Alicante, Spain.
Mercedes GasiorHospital La Paz, Madrid, Spain.
Beatriz BellosilloHospital del Mar, Barcelona, Spain.
Juan-Luis SteegmannHospital de La Princesa, Madrid, Spain.
Alberto Álvarez-LarránHospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.
Jesús María Hernández-RivasHospital Clínico, Salamanca, Spain.
Juan Carlos Hernández-BoludaHospital Clínico Universitario-INCLIVA, Valencia, Spain.
Hospital Universitario de Canarias · ESComplejo Hospitalario Universitario de Santiago · ESConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESHospital Del Mar · ESInstitut Català d'Oncologia · ESDigital Science (United States) · USHebron University · PSHospital Clínico Universitario Virgen de la Victoria · ESHospital Costa del Sol · ESHospital de Sant Pau · ESHospital General Universitario de Alicante Doctor Balmis · ESHospital Jerez Puerta del Sur · ESHospital Universitari i Politècnic La Fe · ESHospital Universitario 12 De Octubre · ESHospital Universitario Central de Asturias · ESHospital Universitario de Gran Canaria Doctor Negrín · ESHospital Universitario La Paz · ESHospital Universitario Virgen de la Arrixaca · ESMarqués de Valdecilla University Hospital · ESUniversidad Católica de Murcia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myelofibrosis (MF) is a myeloproliferative neoplasm (MPN) with heterogeneous clinical course. Allogeneic hematopoietic cell transplantation remains the only curative therapy, but its morbidity and mortality require careful candidate selection. Therefore, accurate disease risk prognostication is critical for treatment decision-making. We obtained registry data from patients diagnosed with MF in 60 Spanish institutions (N = 1386). These were randomly divided into a training set (80%) and a test set (20%). A machine learning (ML) technique (random forest) was used to model overall survival (OS) and leukemia-free survival (LFS) in the training set, and the results were validated in the test set. We derived the AIPSS-MF (Artificial Intelligence Prognostic Scoring System for Myelofibrosis) model, which was based on 8 clinical variables at diagnosis and achieved high accuracy in predicting OS (training set c-index, 0.750; test set c-index, 0.744) and LFS (training set c-index, 0.697; test set c-index, 0.703). No improvement was obtained with the inclusion of MPN driver mutations in the model. We were unable to adequately assess the potential benefit of including adverse cytogenetics or high-risk mutations due to the lack of these data in many patients. AIPSS-MF was superior to the IPSS regardless of MF subtype and age range and outperformed the MYSEC-PM in patients with secondary MF. In conclusion, we have developed a prediction model based exclusively on clinical variables that provides individualized prognostic estimates in patients with primary and secondary MF. The use of AIPSS-MF in combination with predictive models that incorporate genetic information may improve disease risk stratification.

Identifiers

PMID36570691
PMCPMC9771324
OpenAlexW4312211610

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.