Evidence map›Paper›PMID 25246802›Full record

ReviewOncoTargets and therapy2014

Arsenic trioxide-based therapy in relapsed/refractory multiple myeloma patients: a meta-analysis and systematic review.

Xuepeng He, Kai Yang, Peng Chen, Bing Liu, Yuan Zhang, Fang Wang, Zhi Guo, Xiaodong Liu, Jinxing Lou, Huiren Chen

Open access · goldAbstract readReview
In one paragraph

Review in OncoTargets and therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-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

2 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 1 institution in 1 country.

Xuepeng HeDepartment of Hematology, General Hospital of Beijing Military Area of PLA, Beijing, People's Republic of China.
Kai YangDepartment of Hematology, General Hospital of Beijing Military Area of PLA, Beijing, People's Republic of China.
Peng ChenDepartment of Hematology, General Hospital of Beijing Military Area of PLA, Beijing, People's Republic of China.
Bing LiuDepartment of Hematology, General Hospital of Beijing Military Area of PLA, Beijing, People's Republic of China.
Yuan ZhangDepartment of Hematology, General Hospital of Beijing Military Area of PLA, Beijing, People's Republic of China.
Fang WangDepartment of Hematology, General Hospital of Beijing Military Area of PLA, Beijing, People's Republic of China.
Zhi GuoDepartment of Hematology, General Hospital of Beijing Military Area of PLA, Beijing, People's Republic of China.
Xiaodong LiuDepartment of Hematology, General Hospital of Beijing Military Area of PLA, Beijing, People's Republic of China.
Jinxing LouDepartment of Hematology, General Hospital of Beijing Military Area of PLA, Beijing, People's Republic of China.
Huiren ChenDepartment of Hematology, General Hospital of Beijing Military Area of PLA, Beijing, People's Republic of China.
The Military General Hospital of Beijing PLA · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a clonal malignancy characterized by the proliferation of malignant plasma cells in the bone marrow and the production of monoclonal immunoglobulin. Although some newly approved drugs (thalidomide, lenalidomide, and bortezomib) demonstrate significant benefit for MM patients with improved survival, all MM patients still relapse. Arsenic trioxide (ATO) is the most active single agent in acute promyelocytic leukemia, the antitumor activity of which is partly dependent on the production of reactive oxygen species. Due to its multifaceted effects observed on MM cell lines and primary myeloma cells, Phase I/II trials have been conducted in heavily pretreated patients with relapsed or refractory MM. Therapy regimens varied dramatically as to the dosage of ATO and monotherapy versus combination therapy with other agents available for the treatment of MM. Although ATO-based combination treatment was well tolerated by most patients, most trials found that ATO has limited effects on MM patients. However, since small numbers of patients were randomized to different treatment arms, trials have not been statistically powered to determine the differences in progression-free survival and overall survival among the experimental arms. Therefore, large Phase III studies of ATO-based randomized controlled trials will be needed to establish whether ATO has any potential beneficial effects in the clinical setting.

Indexed as

arsenic trioxideclinical trialmeta-analysismultiple myelomatherapy

Identifiers

PMID25246802
PMCPMC4166211
OpenAlexW1995694039

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.