MétaCan
Menu
Back to cohort

Impact of Bone Marrow Fibrosis in MDS Patients Treated with Azacitidine

2016· article· en· W2761565001 on OpenAlexaff
Danielle Hammond, Mina Jamali, Richard A. Wells, Liying Zhang, Alex Mamedov, Martha Lenis, Rena Buckstein

Bibliographic record

VenueBlood · 2016
Typearticle
Languageen
FieldMedicine
TopicMyeloproliferative Neoplasms: Diagnosis and Treatment
Canadian institutionsHealth Sciences CentreSunnybrook Health Science CentreUniversity of Toronto
Fundersnot available
KeywordsMedicineMyelofibrosisAzacitidineInternal medicineInternational Prognostic Scoring SystemMyelodysplastic syndromesChronic myelomonocytic leukemiaBone marrowGastroenterologySurgeryOncology

Abstract

fetched live from OpenAlex

Abstract Background: Myelofibrosis (MF) in primary myelodysplastic syndromes (MDS) is a distinct clinicopathological entity from primary myelofibrosis. In the absence of therapy, it has been shown to be an independent predictor of worse overall survival (OS) and leukemia-free survival (LFS) in both low and high risk MDS (Della Porta, J. Clin. Oncol, 2009). However, there are conflicting reports as to whether this applies to higher-risk patients treated with azacitidine, the recommended first line therapy in this group (Fu, Mod. Pathol, 2014). Methods: 93 consecutive patients from our centre treated with azacitidine for MDS or CMML between 2008 and present were identified from a national prospective MDS registry. The pre-treatment marrows of 53 patients were available for independent and retrospective MF scoring by a hematopathologist (MJ) using both the European Consensus and Bauermeister criteriafor myelofibrosis grading. Qualitative fibrosis status of either none/mild or increased/marked were extracted from original reports in 8 additonal patients for which marrows were not available for hematopathologic review. The remaining patients were excluded due to: >20% blasts pre-treatment (1), lack of pre-treatment bone marrows (20), lack of fibrosis status indicated in original report and marrow not available for review (10), and lack of response data (1). Those with European Consensus MF <2 or qualitatively mild/none were compared to those with MF >or= 2 or qualitatively increased/marked. Patients were also compared as Bauermeister grades 1-2 or mild/none vs. Bauermeister grades 3-4 or increased/marked. Results: Median age of the 61 patients was 72 years and 74% were male. According to WHO classification, 2 had del(5q) syndrome, 5 RARS, 8 RCMD, 16 RAEB-1, 23 RAEB-2, 2 CMML1, 4 CMML2 and 1 MDS/MPN. Median hemoglobin level, neutrophil count, platelet count, LDH, ferritin, and marrow blast count were 91 g/L (range 64-136), 1 x109/L (0-46), 51 x109/L (2-459), 263 U/L (110-1442), 746 mcg/L (56-7983) and 7% (2-18), respectively. 58% were transfusion dependent at start of treatment. IPSS was High, Int-2, Int-1, and Low in 9%, 46%, 33%, and 4% of patients. 32 patients (53%) had European Consensus MF grades >or=2 or increased/marked fibrosis, and this was significantly (p=0.011) associated with higher pre-treatment ferritin levels (1110 vs. 532mcg/L). The increased MF group also showed trends towards younger age (68 vs 72 years), longer time from diagnosis until treatment (18.3 vs. 7.1 mos), greater transfusion dependence (69 vs. 45%), and pre-treatment LDH >250 U/L (61 vs. 42%), which did not meet statistical significance given limited sample size. Otherwise there were no significant relationships between MF score and WHO classification, IPSS/IPSSR, karyotype/cytogenetics, or other covariates. The results were similar when comparing groups by the alternative Bauermeister criteria, with increased fibrosis associated with a ferritin of >1000 mcg/L (p=0.038). After a median of 9 cycles (1-62) of azacitidine,complete remission (CR), marrow CR, and hematologic improvement (HI) was achieved in 9 (15%), 5 (8%), and 27 (44%) patients, respectively. Stable disease was seen in 29 (48%) patients. After a median follow-up of 3 years, median OS by Kaplan-Meier survival curve was 3.6 years in all treated patients and 2.7 years in IPSS Int-2/High patients. Regardless of which fibrosis grading system was used to compare patients, there were no significant differences in time to achieve best response, response rates, OS, or LFS based on pre-treatment MF grades (Figure 1). Conclusion: In this prospective registry series of azacitidine treated MDS with retrospective, pathology reviewed semi-quantitative MF grading, the degree of myelofibrosis did not significantly impact response to azacitidine, progression to leukemia, or overall survival. However, increased fibrosis was significantly associated with higher pre-treatment ferritin values and resulted in a non-significant trend towards younger age, longer time to treatment, transfusion dependence, and higher pre-treatment LDH levels. Figure 1 Overall Survival by MF Grade Figure 1. Overall Survival by MF Grade Disclosures Wells: Novartis: Honoraria, Membership on an entity's Board of Directors or advisory committees; Celgene: Honoraria, Membership on an entity's Board of Directors or advisory committees; Alexion: Honoraria, Membership on an entity's Board of Directors or advisory committees. Buckstein:Novartis: Honoraria; Celgene: Honoraria, Research Funding.

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)0.000
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.006

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

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 head0.009
GPT teacher head0.246
Teacher spread0.237 · 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 designObservational
Domainnot available
GenreEmpirical

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".

Quick stats

Citations3
Published2016
Admission routes1
Has abstractyes

Explore more

Same venueBloodSame topicMyeloproliferative Neoplasms: Diagnosis and TreatmentFrench-language works237,207