Evidence map›Paper›PMID 26740870›Full record

ArticleMediterranean journal of hematology and infectious diseases2016

Treatment with Low-Dose Cytarabine in Elderly Patients (Age 70 Years or Older) with Acute Myeloid Leukemia: A Single Institution Experience.

Maël Heiblig, Mohamed Elhamri, Isabelle Tigaud, Adriana Plesa, Fiorenza Barraco, Hélène Labussière, Sophie Ducastelle, Mauricette Michallet, Franck Nicolini, Claudiu Plesa and 3 more

Abstract read
In one paragraph

Article in Mediterranean journal of hematology and infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Review
  6. Review
  7. Venetoclax-based therapies for acute myeloid leukemia.Best practice & research. Clinical haematology · 2019
    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

13 authors.

Maël HeibligDepartment of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre Bénite, France.
Mohamed ElhamriDepartment of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre Bénite, France.
Isabelle TigaudLaboratory of Cytogenetics, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre Bénite, France.
Adriana PlesaLaboratory of Cytology and Immunology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre Bénite, France.
Fiorenza BarracoDepartment of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre Bénite, France.
Hélène LabussièreDepartment of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre Bénite, France.
Sophie DucastelleDepartment of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre Bénite, France.
Mauricette MichalletDepartment of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre Bénite, France.
Franck NicoliniDepartment of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre Bénite, France.
Claudiu PlesaTrarieux Clinic, Lyon, France.
Eric WattelDepartment of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre Bénite, France.
Gilles SallesDepartment of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre Bénite, France.
Xavier ThomasDepartment of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre Bénite, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesLow-dose cytarabine (LD-AraC) is still regarded as the standard of care in elderly patients with acute myeloid leukemia (AML) 'unfit' for intensive chemotherapy. In this study, we reported our experience with LD-AraC in patients ≥ 70 years old and compared the results to those of intensive chemotherapy, best supportive care (BSC), or hypomethylating agents in the same age population.

methodsBetween 2000 and 2014, 60 patients received LD-AraC at 20 mg once or twice daily by subcutaneous injection for 10 consecutive days every 4-6 weeks.

resultsComplete remission rate with LD-AraC was 7% versus 56% with intensive chemotherapy and 21% with hypomethylating agents. Median overall survival (OS) of patients treated with LD-AraC was 9.6 months with 3-year OS of 12%. Survival with LD-AraC was better than with BSC only (P = 0.001). Although not statistically significant, intensive chemotherapy and hypomethylating agents tended to be better than LD-AraC in terms of OS (median: 12.4 months and 16.1 months, respectively). There was no clear evidence that a beneficial effect of LD-AraC was restricted to any particular subtype of patients, except for cytogenetics. There was a trend for a better OS in LD-AraC treated patients in the setting of clinical trials as compared with those treated outside of a clinical trial.

conclusionsDespite a trend in favor of intensive chemotherapy and hypomethylating agents over LD-AraC, no real significant advantage could be demonstrated, while LD-AraC showed a significant advantage comparatively to BSC. All this tends to confirm that LD-AraC can still represent a baseline against which new promising agents may be compared either alone or in combination.

Identifiers

PMID26740870
PMCPMC4696467

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.