Evidence map›Paper›PMID 15914366›Full record

Trial reportInternational journal of hematology2005

The maturation of myeloma cells correlates with sensitivity to chemotherapeutic agents.

Yoshiaki Kuroda, Akira Sakai, Yoshiko Okikawa, Shoso Munemasa, Yuta Katayama, Hideo Hyodo, Jun Imagawa, Yasuo Takimoto, Hajime Okita, Megu Ohtaki and 1 more

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in International journal of hematology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact, top 89% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Plasma cell maturity as a predictor of prognosis in multiple myeloma.Medical oncology (Northwood, London, England) · 2016
    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

11 authors at 2 institutions in 1 country.

Yoshiaki KurodaDepartment of Hematology and Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima734-8553, Japan.
Akira Sakai
Yoshiko Okikawa
Shoso Munemasa
Yuta Katayama
Hideo Hyodo
Jun Imagawa
Yasuo Takimoto
Hajime Okita
Megu Ohtaki
Akiro Kimura
Hiroshima University · JPKobatake Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We analyzed both morphologic and phenotypic findings of myeloma cells before and after chemotherapy in 21 patients with multiple myeloma. The morphologic analysis was based on the Greipp classification, and phenotypic analysis was performed by 3-color flow cytometry using the CD38 plasma gating method (Marrow plasma 38). Results with flow cytometry using a combination of MPC1, CD49e, and CD45 supported the morphologic findings for the myeloma cells. Treatment with 3 or 4 cycles of VAD (vincristine, doxorubicin, and dexamethasone) therapy was effective in reducing the total numbers of myeloma cells, but the proportion of immature myeloma cells increased after this treatment. However, the immature myeloma cells were reduced by high-dose melphalan (HD-Mel) therapy followed by autologous stem cell transplantation (ASCT). High-dose cyclophosphamide treatment for stem cell harvesting did not show an effect on the residual immature myeloma cells after VAD treatment. In addition, thalidomide was not effective in reducing the numbers of immature myeloma cells. These results suggest that VAD (3 or 4 cycles) therapy plus HD-Mel followed by ASCT is a reasonable treatment for multiple myeloma and that Marrow plasma 38 analysis is a useful method for monitoring the response of multiple myeloma to chemotherapy.

Indexed as

ADP-ribosyl CyclaseADP-ribosyl Cyclase 1AgedAntigens, CDAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsCell DifferentiationCyclophosphamideDexamethasoneDoxorubicinDrug Resistance, NeoplasmFemaleFlow CytometryHumansMaleMelphalanADP-ribosyl CyclaseADP-ribosyl Cyclase 1Antigens, CDAntineoplastic AgentsCD38 protein, humanCyclophosphamideDexamethasoneDoxorubicinMelphalanMembrane GlycoproteinsPrednisoneVincristine

Identifiers

PMID15914366
OpenAlexW2082799476

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.