Evidence map›Paper›PMID 27434660›Full record

ArticleBritish journal of haematology2016

Haematopoietic cell transplantation with and without sorafenib maintenance for patients with FLT3-ITD acute myeloid leukaemia in first complete remission.

Andrew M Brunner, Shuli Li, Amir T Fathi, Martha Wadleigh, Vincent T Ho, Kerry Collier, Christine Connolly, Karen K Ballen, Corey S Cutler, Bimalangshu R Dey and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of haematology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed, 3 pooled it
19.1field-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.

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

90 citing papers in PubMed, 3 syntheses or guidelines pooled it, 174 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Reduced-Intensity Conditioning Followed by Related and Unrelated Allografts for Hematologic Malignancies: Expanded Analysis and Long-Term Follow-Up.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Trial
  7. Article
  8. Article
  9. Review
  10. Review
  11. Clinical Outcomes and Treatment Patterns in Adults With FLT3-ITDTransplantation and cellular therapy · 2024
    Observational
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Sorafenib in Combination With Standard Chemotherapy for Children With High Allelic RatioJournal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    Article

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

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

21 authors at 2 institutions in 1 country.

Andrew M BrunnerMassachusetts General Hospital, Boston, MA, USA.
Shuli LiDana-Farber Cancer Institute, Boston, MA, USA.
Amir T FathiMassachusetts General Hospital, Boston, MA, USA.
Martha WadleighDana-Farber Cancer Institute, Boston, MA, USA.
Vincent T HoDana-Farber Cancer Institute, Boston, MA, USA.
Kerry CollierMassachusetts General Hospital, Boston, MA, USA.
Christine ConnollyMassachusetts General Hospital, Boston, MA, USA.
Karen K BallenMassachusetts General Hospital, Boston, MA, USA.
Corey S CutlerDana-Farber Cancer Institute, Boston, MA, USA.
Bimalangshu R DeyMassachusetts General Hospital, Boston, MA, USA.
Areej El-JawahriMassachusetts General Hospital, Boston, MA, USA.
Sarah NikiforowDana-Farber Cancer Institute, Boston, MA, USA.
Steven L McAfeeMassachusetts General Hospital, Boston, MA, USA.
John KorethDana-Farber Cancer Institute, Boston, MA, USA.
Daniel J DeangeloDana-Farber Cancer Institute, Boston, MA, USA.
Edwin P AlyeaDana-Farber Cancer Institute, Boston, MA, USA.
Joseph H AntinDana-Farber Cancer Institute, Boston, MA, USA.
Thomas R SpitzerMassachusetts General Hospital, Boston, MA, USA.
Richard M StoneDana-Farber Cancer Institute, Boston, MA, USA.
Robert J SoifferDana-Farber Cancer Institute, Boston, MA, USA.
Yi-Bin ChenMassachusetts General Hospital, Boston, MA, USA. ychen6@partners.org.
Dana-Farber Cancer Institute · USMassachusetts General Hospital · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI A. Heather Eliassen · 1985 to 2026
$330.6M
Dana Farber/Harvard Cancer Consortium Career Development Program in Clinical OncologyK12CA087723 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI David Tsai Ting · 2002 to 2026
$17.9M
Training Program in Cancer Biology and TherapeuticsT32CA071345 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Daniel A. Haber, Lecia V. Sequist · 1997 to 2026
$10.6M
Manipulation of Immune Responsiveness after Hematopoietic Cell TransplantationR01CA183559 · NCI · DANA-FARBER CANCER INST · PI RITZ, JEROME, SOIFFER, ROBERT JON · 2013 to 2017
$3.7M
NCI NIH HHS K12 CA087723NCI NIH HHS P30 CA006516NCI NIH HHS R01 CA183559NCI NIH HHS T32 CA071345
6 · The paper itself

Abstract

We performed a retrospective study analysing the effect of sorafenib, an oral fms-Like Tyrosine Kinase 3 (FLT3)/multikinase inhibitor, as post-transplant maintenance in adult patients with FLT3-internal tandem duplication (ITD) acute myeloid leukaemia (AML). We identified consecutive patients with FLT3-ITD AML diagnosed between 2008 and 2014 who received haematopoietic cell transplantation (HCT) in first complete remission (CR1). Post-HCT initiation of sorafenib (yes/no) was evaluated as a time-varying covariate in the overall survival/progression-free survival (OS/PFS) analysis and we performed a landmark analysis of controls alive without relapse at the median date of sorafenib initiation. We identified 26 sorafenib patients and 55 controls. Median follow-up was 27·2 months post-HCT for sorafenib survivors, and 38·4 months for controls (P = 0·021). The median time to initiating sorafenib was 68 days post-HCT; 43 controls were alive without relapse at this cut-off. Sorafenib patients had improved 2-year OS in the d+68 landmark analysis (81% vs. 62%, P = 0·029). Sorafenib was associated with improved 2-year PFS (82% vs. 53%, P = 0·0081) and lower 2-year cumulative incidence of relapse (8·2% vs. 37·7%, P = 0·0077). In multivariate analysis, sorafenib significantly improved OS [Hazard ratio (HR) 0·26, P = 0·021] and PFS (HR 0·25, P = 0·016). There was no difference in 2-year non-relapse mortality (9·8% vs. 9·3%, P = 0·82) or 1-year chronic graft-versus-host disease (55·5% vs. 37·2%, P = 0·28). These findings suggest potential benefit of post-HCT sorafenib in FLT3-ITD AML, and support further evaluation of post-HCT FLT3 inhibition.

Indexed as

Hematopoietic Stem Cell TransplantationTandem Repeat SequencesAdultAgedAntineoplastic AgentsCombined Modality TherapyFemalefms-Like Tyrosine Kinase 3HumansLeukemia, Myeloid, AcuteMaintenance ChemotherapyMaleMiddle AgedNiacinamidePhenylurea CompoundsProtein Kinase InhibitorsAntineoplastic Agentsfms-Like Tyrosine Kinase 3NiacinamidePhenylurea CompoundsProtein Kinase InhibitorsSorafenibacute myeloid leukaemiaallogeneic transplantationfms-Like Tyrosine Kinase 3maintenance chemotherapysorafenib

Identifiers

PMID27434660
PMCPMC5083189
OpenAlexW2502940040

What OpenQuestion holds

Textmetadata
LicenceTDM
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.