Evidence map›Paper›PMID 22980425›Full record

ReviewJournal of hematology & oncology2012

Therapeutic advancement of chronic lymphocytic leukemia.

Kang Lu, Xin Wang

Abstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–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

23 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. A Comparison of Cytotoxic Effects ofIranian journal of pharmaceutical research : IJPR · 2019
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Ibrutinib for B cell malignancies.Experimental hematology & oncology · 2014
    Article
  12. Role of high expression of IL-9 in prognosis of CLL.International journal of clinical and experimental pathology · 2014
    Article
  13. Article
  14. Article
  15. STAT inhibitors for cancer therapy.Journal of hematology & oncology · 2013
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Ibrutinib and novel BTK inhibitors in clinical development.Journal of hematology & oncology · 2013
    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

2 authors.

Kang LuDepartment of Hematology, Provincial Hospital Affiliated to Shandong University, No, 324 Jingwu Road, Jinan, Shandong, 250021, P R China.
Xin Wang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the combinations of chemotherapy with monoclonal antibodies have further improved response rates, chronic lymphocytic leukemia (CLL) remains an incurable disease with an extremely variable course. This article reviews the ongoing clinical advances in the treatment of CLL in both previously untreated and relapsed disease and focuses on the benefit of different therapeutic strategies, the most effective therapy combinations and the potential activity of novel agents. Novel agents and combination therapies have been investigated by several studies in both the upfront and relapsed setting, particularly for patients with 17p deletion, TP53 mutation and fludarabine-refractory CLL. While these agents and combination therapies have improved initial response rates, ongoing studies are continued to determine and improve the efficacy and safety. Despite advancements in the treatment of CLL have led to high response rates, allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains the only curative option and reduced-intensity conditioning (RIC) allo-HSCT must be strongly considered whenever feasible. As such, ongoing studies of these agents and other novel approaches in clinical development are needed to expand and improve treatment options for CLL patients.

Indexed as

AgedAntibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsCombined Modality TherapyFemaleHumansLeukemia, Lymphocytic, Chronic, B-CellMaleMiddle AgedAntibodies, Monoclonal

Identifiers

PMID22980425
PMCPMC3465197

What OpenQuestion holds

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Registered trials

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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.