Evidence map›Paper›PMID 20085935›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2010

Single cycle of arsenic trioxide-based consolidation chemotherapy spares anthracycline exposure in the primary management of acute promyelocytic leukemia.

Steven D Gore, Ivana Gojo, Mikkael A Sekeres, Lawrence Morris, Marcel Devetten, Katarzyna Jamieson, Robert L Redner, Robert Arceci, Ibitayo Owoeye, Tianna Dauses and 2 more

Open access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 3% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 88 citations in OpenAlex.

  1. Pooled it
  2. Arsenic trioxide replacing or reducing chemotherapy in consolidation therapy for acute promyelocytic leukemia (APL2012 trial).Proceedings of the National Academy of Sciences of the United States of America · 2021
    Trial
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

12 authors at 4 institutions in 1 country.

Steven D GoreSidney Kimmel Comprehensive Cancer Center at Johns Hopkins, CRB1-288, 1650 Orleans St, Baltimore, MD 21231, USA. gorest@jhmi.edu
Ivana Gojo
Mikkael A Sekeres
Lawrence Morris
Marcel Devetten
Katarzyna Jamieson
Robert L Redner
Robert Arceci
Ibitayo Owoeye
Tianna Dauses
Esther Schachter-Tokarz
Robert E Gallagher
University of Maryland, Baltimore · USSidney Kimmel Comprehensive Cancer Center · USUniversity of Pittsburgh · USUniversity of Iowa · US

Funding

Arsenic Trioxide in Primary Curative APL TherapyR01CA100904 · NCI · JOHNS HOPKINS UNIVERSITY · PI GORE, STEVEN D · 2004 to 2008
$2.3M
Targeting Epigenomics in Myeloid NeoplasmsK24CA111717 · NCI · YALE UNIVERSITY · PI GORE, STEVEN D · 2005 to 2015
$1.7M
NCI NIH HHS K24 CA111717NCI NIH HHS R01 CA100904
6 · The paper itself

Abstract

PURPOSE Event-free survival following all-trans-retinoic acid (ATRA) -based therapy for acute promyelocytic leukemia (APL) averages 70% at 5 years. While arsenic trioxide (ATO) can induce remissions in 95% of relapsed patients, few studies have addressed the integration of ATO into the primary management of APL. This study examines the efficacy of a single cycle of ATO-based consolidation therapy in a treatment regimen designed to decrease exposure to other cytotoxic agents. PATIENTS AND METHODS After induction with ATRA and daunorubicin (DRN), untreated patients with APL received 3 days of cytarabine and DRN followed by 30 doses of ATO beginning on day 8. Molecular remitters received 2 years of risk-based maintenance therapy. Results Forty-one of 45 patients receiving induction therapy achieved remission; four patients died (one before treatment was initiated). Thirty-seven patients received consolidation and maintenance; of these one patient relapsed (CNS) and one died in remission during maintenance therapy (hepatic sickle cell crisis). With a median follow-up of 2.7 years, estimated disease-free survival was 90%; overall survival for all patients was 88%. Despite a total anthracycline dose of only 360 mg/m(2), cardiac ejection fraction decreased by > or = 20% in 20% of patients. CONCLUSION These data, combined with other recent studies using ATO in the primary management of APL, demonstrate the important role that ATO can play in the primary management of this curable disease. Future studies should continue to focus on reducing the toxicity of treatment without increasing the relapse rate.

Indexed as

AdolescentAdultAgedAntineoplastic Combined Chemotherapy ProtocolsArsenicalsArsenic TrioxideChildChild, PreschoolCytarabineDaunorubicinFemaleHumansLeukemia, Promyelocytic, AcuteMaleMiddle AgedNeoplasm Recurrence, LocalArsenicalsArsenic TrioxideCytarabineDaunorubicinOxidesTretinoin

Identifiers

PMID20085935
PMCPMC2834430
OpenAlexW2096318892

What OpenQuestion holds

Textmetadata
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.