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Thrombopoietin (TPO)-Receptor Agonists In Myelodysplastic Syndromes (MDS): A Systematic Review and Meta-Analysis

2013· review· en· W48554944 on OpenAlexaff
Anca Prica, Michelle Sholzberg, Rena Buckstein

Bibliographic record

VenueBlood · 2013
Typereview
Languageen
FieldMedicine
TopicPlatelet Disorders and Treatments
Canadian institutionsSt. Michael's HospitalHealth Sciences CentreSunnybrook Health Science Centre
Fundersnot available
KeywordsEltrombopagRomiplostimMedicineMyelodysplastic syndromesThrombopoietin receptorThrombopoietinLenalidomideInternal medicineRandomized controlled trialPlaceboOncologyPlateletBone marrowMultiple myeloma

Abstract

fetched live from OpenAlex

Abstract Background Thrombocytopenia is a common (40-65%) manifestation of MDS. The incidence of bleeding ranges from 3% to 56% encompassing minor bleeds such as petechiae and gingival bleeding, and more serious bleeds (18%), such as gastrointestinal (GI, 6-7%) and intracranial (3-5%) bleeding. Lenalidomide and azacitidine are not specifically used or approved for the treatment of thrombocytopenia in MDS and while effective in some patients, may in fact engender a thrombocytopenia that is dose limiting. The interaction between thrombopoietin (TPO) and its receptor c-Mpl is essential for platelet production. Romiplostim and Eltrombopag are two TPO-receptor agonists presently approved by the FDA. They have been tested in MDS, with some evidence of benefit, but there are safety concerns regarding progression to acute myeloid leukemia (AML). Purpose To determine the safety, as well as the clinical outcomes of adding a TPO-receptor agonist to standard treatment in patients with myelodysplastic syndromes. Methods A systematic literature search strategy was conducted up to February 2013, using MEDLINE, EMBASE, the Cochrane Register of Controlled Trials, as well as conference proceedings. All randomized controlled trials (RCTs) that enrolled adult patients with myelodysplastic syndromes were included if the RCT compared a TPO-R agonist (Romiplostim or Eltrombopag) to placebo or no treatment. A meta-analysis of the effects was performed. Pooled treatment effects were calculated as risk ratios (RR) for binary data, using a random effects model. Bleeding and platelet transfusion rates were also reported as exposure-adjusted rates per patient-month, as it was felt to be a meaningful time period for this disease. The exposure adjusted rate was defined as the number of events per person-time at risk and captures the total cumulative bleeding events (even multiple events within the same patient). Months of person time were defined as months from first dose date to study end date. Results Four RCTs met all inclusion criteria, and a total of 358 patients were included in the systematic review. 2 studies included only lower risk MDS patients (IPSS low/int-1) and 2 studies included lower and higher risk patients (IPSS low/int-1 and int-2). Romiplostim was compared to placebo in all 4 trials, but each trial had a different backbone for MDS therapy (lenalidomide, azacitidine, decitabine and just placebo). Two trials compared 2 dosing regimens to placebo (500ug weekly and 750ug weekly) and 2 trials used the higher dosing of 750ug weekly. Three studies of eltrombopag vs. placebo are ongoing, and results were not available for inclusion. Relative risk (RR) of bleeding with romiplostim vs. placebo was 0.84 (95% CI: 0.57-1.24; I2:12%). Exposure-adjusted bleeding rate per patient month was significantly less with romiplostim vs. placebo at 0.92 (95% CI: 0.86-0.99; I2:0%). Only one study reported severe grade 3-4 bleeding events, and the rates were very low, at 1/27 in the intervention arms (4%) and 2/13 (13%) in the control group, giving a favourable RR of 0.24, but very wide 95% CI of 0.02 to 2.42. The exposure-adjusted platelet transfusion rate per patient month was also significantly less with romiplostim at 0.69 (95% CI: 0.53-0.88; I2:34%). The RR of AML progression with romiplostim vs. placebo was 1.36 (95% CI: 0.54-3.40; I2:0%), however the AML progression outcome data were felt to be at high risk of bias because of the early termination of one trial. Mortality was reported as a proportion of deaths during the study period for all 4 trials, giving a RR with romiplostim of 0.90 (95% CI: 0.54-1.50; I2: 30%). Conclusions Romiplostim is promising in its ability to decrease patient-important outcomes: cumulative bleeding events and the need for platelet transfusions. However, most of those bleeding events were likely grade 2, which are not necessarily clinically important, and platelet transfusion reduction may not be as relevant for those practicing therapeutic (not prophylactic) platelet transfusions. Although the risk of AML progression was not increased, the outcome data were felt to be at high risk for bias, and thus this safety concern cannot be ignored. Therefore, romiplostim cannot yet be routinely recommended. Results of ongoing eltrombopag studies are awaited. Disclosures: No relevant conflicts of interest to declare.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.008
metaresearch head score (Gemma)0.018
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Meta-analysis · Consensus signal: none
GenreCandidate signal: Review · Consensus signal: Review
Teacher disagreement score0.020
Threshold uncertainty score0.042

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0080.018
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0200.025
Bibliometrics0.0070.009
Science and technology studies0.0010.001
Scholarly communication0.0020.002
Open science0.0020.001
Research integrity0.0020.001
Insufficient payload (model declined to judge)0.0050.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.066
GPT teacher head0.334
Teacher spread0.268 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designMeta-analysis
Domainnot available
GenreReview

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations6
Published2013
Admission routes1
Has abstractyes

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