Evidence map›Paper›PMID 28674026›Full record

ArticleBlood2017

Clonal evolution and outcomes in myelofibrosis after ruxolitinib discontinuation.

Kate J Newberry, Keyur Patel, Lucia Masarova, Rajyalakshmi Luthra, Taghi Manshouri, Elias Jabbour, Prithviraj Bose, Naval Daver, Jorge Cortes, Hagop Kantarjian and 1 more

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 121 papers.

0numbers the graph read from it
0cells of the map it votes in
121citing papers in PubMed
11.5field-weighted citation impact, top 1% 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.

NCT03959371 unknown statusnot on this map

Observational, Retrospective and Prospective Study on the Use of Ruxolitinib in Myelofibrosis Patients in Lombardy, Italy

TypeobservationalSponsorMargherita MaffioliRan2017 to 2021Enrolled620ConditionsMyelofibrosisArmsRuxolitinib
NCT04103645 phase2terminatednot on this mapstarted 2019, after this paper: background citation

A 2-tiered, Phase 2, Rule-based, Intra-patient Dose Escalation Study to Investigate Safety and Feasibility of Vactosertib (TEW-7197) in the Treatment of Anemic Patients With Philadelphia Chromosome-negative MPNs (Ph-neg MPNs)

TypeinterventionalSponsorWeill Medical College of Cornell UniversityRan2019 to 2024Enrolled2ConditionsMyeloproliferative NeoplasmArmsVactosertib
3 · Its place in the literature

Who cites it

121 citing papers in PubMed, 213 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. MANIFEST: Pelabresib in Combination With Ruxolitinib for Janus Kinase Inhibitor Treatment-Naïve Myelofibrosis.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Article
  11. Article
  12. Review
  13. Review
  14. The Role and Impact of Non-driver Gene Mutations in Myelofibrosis.Current hematologic malignancy reports · 2026
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

61 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Kate J NewberryDepartment of Leukemia and.
Keyur PatelDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Lucia MasarovaDepartment of Leukemia and.
Rajyalakshmi LuthraDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Taghi ManshouriDepartment of Leukemia and.
Elias JabbourDepartment of Leukemia and.
Prithviraj BoseDepartment of Leukemia and.
Naval DaverDepartment of Leukemia and.
Jorge CortesDepartment of Leukemia and.
Hagop KantarjianDepartment of Leukemia and.
Srdan VerstovsekDepartment of Leukemia and.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Despite significant improvements in the signs and symptoms of myelofibrosis (MF), and possible prolongation of patients' survival, some have disease that is refractory to ruxolitinib and many lose their response over time. Furthermore, patients with ≥3 mutations are less likely to respond to ruxolitinib. Here we describe outcomes after ruxolitinib discontinuation in MF patients enrolled in a phase 1/2 study at our center. After a median follow-up of 79 months, 86 patients had discontinued ruxolitinib (30 of whom died while on therapy). The median follow-up after ruxolitinib discontinuation for the remaining 56 patients was 32 months, with median survival after discontinuation of 14 months. Platelets <260 × 10

Indexed as

Withholding TreatmentAdultAgedAged, 80 and overClonal EvolutionFemaleHumansKaplan-Meier EstimateMaleMiddle AgedNitrilesPrimary MyelofibrosisPyrazolesPyrimidinesTreatment OutcomeNitrilesPyrazolesPyrimidinesruxolitinib

Identifiers

PMID28674026
PMCPMC5580275
OpenAlexW2731573311

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.