MétaCan
Menu
Back to cohort
Record W4405047930 · doi:10.1182/blood-2024-204999

Prognostic Implication of Framingham Risk Score As a Comorbidity Measure on Treatment Outcomes Following First-Line Tyrosine Kinase Inhibitor in Newly Diagnosed CML Patients

2024· article· en· W4405047930 on OpenAlexaffabout
May Chiu, María Agustina Perusini, Jaeyoon Kim, Danielle Pyne, Muzaffar Bhatti, Anthea Travas, Oyeronke Ayansola, Amirtha Ambalavanan, Jenny Ho, Dennis Dong Hwan Kim

Bibliographic record

VenueBlood · 2024
Typearticle
Languageen
FieldMedicine
TopicChronic Myeloid Leukemia Treatments
Canadian institutionsLondon Health Sciences CentrePrincess Margaret Cancer CentreUniversity Health Network
Fundersnot available
KeywordsMedicineComorbidityInternal medicineFramingham Risk ScoreTyrosine-kinase inhibitorOncologySecond line treatmentTyrosine kinaseDiseaseCancerOverall survival

Abstract

fetched live from OpenAlex

Introduction Comorbidities, including cardiovascular (CV) disease and risk factors, are crucial in selecting tyrosine kinase inhibitors (TKIs) for chronic myeloid leukemia (CML) patients (pts). About 40-60% of CML pts have at least 1 comorbid condition, and 30% present with CV risk factors at diagnosis. While the Framingham Risk Score (FRS) assesses the 10-year CV risk events in general population and is suggested to be accounted in the TKI selection in CML pts, prospective data on its impact on TKI choice and outcomes is limited. Patients and method The TCGA-GTA project, started in November 2020, is an ongoing, prospective, non-interventional registry study of newly diagnosed CML patients in the Greater Toronto Area, Canada. At initial evaluation, comorbidities and FRS were assessed. Pts with low FRS have ≤10% CV risk at 10 years, intermediate risk is 10-20%, and high risk is >20%. Event-free survival (EFS), failure-free survival (FFS), and TKI-switch-free survival were compared between pts with low FRS (FRSlow) and those with intermediate to high FRS (FRSint/hi). Events included TKI switch, treatment failure (TF), or death, with TF defined by European LeukemiaNet (ELN) 2013 guidelines. Results From Nov 2020 to Jun 30, 2024, the study enrolled 101 newly diagnosed CML pts. Of these, 74.3% were in the FRSlow group and 25.7% in the FRSint/hi group. The median age was 49 years, with the FRSint/hi cohort being older (67.5 vs. 41 years, p<0.001). Males constituted 59% of the the FRSlow group vs. 81% of the FRSint/high group (p=0.057). Chronic phase presentation was seen in 96% of the FRSlow group and 92.3% of the FRSint/hi group. High-risk cytogenetic abnormalities were present in 9.5% of the FRSlow group and 7.7% of the FRSint/hi group. The median SOKAL score was 0.8 in the FRSlow and 0.9 in the FRSint/hi group (p=0.198). The median EUTOS score was 1.25 in the FRSlow and 1.80 in FRSint/hi group (p=0.001). Comorbidities were present in 44% of patients, with hypertension (27.7%) and hyperlipidemia (25.7%) being most common, followed by diabetes mellitus (12.9%), chronic lung disease (11.9%), and vascular disease (9.9%), including coronary artery disease, stroke and peripheral vascular disease. Comorbidities were more prevalent in the FRSint/hi cohort (80.8% vs. 30.7%, p<0.001), with a median of 3 vs. 0 comorbidities per patient. Imatinib was more frequently prescribed in the FRSint/hi group (69.2% vs. 14.9%), while 2nd generation (2G) TKI were more common in the FRSlow group including nilotinib (40.5%) and dasatinib (36.5%). With a median follow-up of 21.3 months, the FRSint/hi group had more adverse events (AEs) (56% vs. 38.6%, p=0.161), including gastrointestinal AEs (19.2% vs. 5.4%, p=0.049) and fatigue (15.4% vs. 1.4%, p=0.016). Overall, 66% of pts achieved BCR::ABL1 <10% at 3 months, 60.5% achieved BCR::ABL1 <1% at 6 months, and 71.9% achieved BCR::ABL1 <0.1% at 12 months. These molecular response rates were higher in the FRSlow group but the differences were not statistically significant. Twenty-seven percent experienced TF, and 31% required a TKI switch, with higher rates in the FRSint/hi cohort. Resistance was the main reason for switching therapy (17.6% in the FRSlow vs. 23.1% in FRSint/hi), followed by intolerance (12.2% in FRSlow vs. 15.4% in the FRSint/hi). At 12 months, EFS and FFS were 69.6% and 75.4% in the FRSlow group vs. 57.2% and 66% in the FRSint/hi group. The probability of remaining on the 1L TKI was also higher in the FRSlow group (67% vs. 49.8%, p=0.142). Progression to advanced phase was similar between the groups (4-5% at 12 months). Multivariable analysis showed that the type of TKI was the only independent factor associated with EFS, FFS, and TKI-switch/discontinuation-free survival, with 2G-TKIs demonstrating superior outcomes compared to imatinib. Conclusion FRS is a key tool for evaluating CV comorbidities and guiding the choice of 1L TKI in CML practice, with FRSint/hi group more likely to receive imatinib. However, intolerance and resistance to imatinib remain significant issues in the FRSint/hi group, and FRS itself does not independently predict treatment outcomes. The type of 1L TKI drug is the most important independent factor influencing treatment outcomes, with 2G-TKIs showing superior results compared to imatinib. Therefore, there is an unmet need for alternative treatments with better efficacy and tolerability, such as asciminib, in the FRSint/hi group.

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)0.001
metaresearch head score (Gemma)0.003
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 score0.016
Threshold uncertainty score0.033

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.003
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

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 head0.020
GPT teacher head0.281
Teacher spread0.261 · 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

Citations0
Published2024
Admission routes2
Has abstractyes

Explore more

Same venueBloodSame topicChronic Myeloid Leukemia TreatmentsFrench-language works237,207