Evidence map›Paper›PMID 19767778›Full record

ArticleBone marrow transplantation2010

Improved outcome of refractory Langerhans cell histiocytosis in children with hematopoietic stem cell transplantation in Japan.

K Kudo, S Ohga, A Morimoto, Y Ishida, N Suzuki, D Hasegawa, Y Nagatoshi, S Kato, E Ishii

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Article in Bone marrow transplantation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Review
  3. Langerhans Cell Histiocytosis: Single Center Experience of 25 Years.Mediterranean journal of hematology and infectious diseases · 2019
    Article
  4. Article
  5. Article
  6. Liver involvement of Langerhans' cell histiocytosis in children.International journal of clinical and experimental medicine · 2015
    Article
  7. Article
  8. Transplantation in rare lymphoproliferative and histiocytic disorders.Cancer control : journal of the Moffitt Cancer Center · 2014
    Review
  9. Article
  10. FrequentBiomedical reports · 2013
    Article
  11. Article
  12. 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

9 authors at 7 institutions in 1 country.

K KudoDivision of Hematology and Oncology, Shizuoka Children's Hospital, Shizuoka, Japan. kazukok@med.nagoya-u.ac.jp
S Ohga
A Morimoto
Y Ishida
N Suzuki
D Hasegawa
Y Nagatoshi
S Kato
E Ishii
Japan Pediatric Society · JPEhime University · JPKobe Children's Hospital · JPKyushu University · JPNational Hospital Organization Kyushu Cancer Center · JPShizuoka Children's Hospital · JPSt. Luke's International Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Langerhans cell histiocytosis (LCH) that is refractory to conventional chemotherapy has a poor outcome. Hematopoietic stem cell transplantation (SCT) is a promising approach for refractory LCH because of its immunomodulatory effect. In this study, the outcomes of children with refractory LCH undergoing SCT in Japan were analyzed. Between November 1995 and March 2007, 15 children younger than 15 years (9 males, 6 females) with refractory LCH underwent SCT. The patients' median age at diagnosis was 8 months (range, 28 days to 28 months), and all had failed conventional chemotherapy. The median age at SCT was 23 months (range, 13-178 months). Nine had risk organ involvement at diagnosis, including liver (n=6), spleen (n=5), lung (n=5), and/or hematopoietic system (n=4). For SCT, a myeloablative regimen was used for 10 patients, and a reduced-intensity conditioning regimen (RIC) was used for five. The donor source varied among the patients, but allogeneic cord blood was primarily used (n=10). Subsequently, 11 of 15 patients have survived with no evidence of disease, with a 10-year overall survival (OS) rate (median+/-standard error) of 73.3+/-11.4%. The 10-year OS rate of nine patients with risk organ involvement at diagnosis was 55.6+/-16.6%, whereas six without risk organ involvement have all survived with no evidence of disease (P=0.07). These results indicate that SCT is promising as a salvage approach for children with refractory LCH.

Indexed as

Hematopoietic Stem Cell TransplantationAntineoplastic Combined Chemotherapy ProtocolsChild, PreschoolFemaleHistiocytosis, Langerhans-CellHumansInfantInfant, NewbornJapanMaleSurvival RateTissue DonorsTreatment Outcome

Identifiers

PMID19767778
OpenAlexW2152707173

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.