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Record W4310119285 · doi:10.1182/blood-2022-169406

Real-World Outcomes and Adverse Events of Elderly Patients with Ph-Negative Acute Lymphoblastic Leukemia Treated with a Pediatric-Inspired Protocol

2022· article· en· W4310119285 on OpenAlexaff
María Agustina Perusini, Jad Sibai, Eshetu G. Atenafu, Aniket Bankar, Mark D. Minden, Vikas Gupta, Dawn Maze, Marta Davidson, Steven M. Chan, Aaron D. Schimmer, Guillaume Richard‐Carpentier, Josephine Anne Lucero, Claire Andrews, Dennis Dong Hwan Kim, Karen Yee, Andre C. Schuh, Hassan Sibai

Bibliographic record

VenueBlood · 2022
Typearticle
Languageen
FieldMedicine
TopicAcute Lymphoblastic Leukemia research
Canadian institutionsPrincess Margaret Cancer CentreUniversity of TorontoUniversity Health Network
Fundersnot available
KeywordsMedicineAdverse effectRegimenInduction chemotherapyConfidence intervalAsparaginaseProportional hazards modelChemotherapy regimenInternal medicinePediatricsChemotherapyLymphoblastic LeukemiaLeukemia

Abstract

fetched live from OpenAlex

Poor outcomes in elderly patients with Acute Lymphoblastic Leukemia (ALL) result from the disease's adverse biology and poor tolerance to chemotherapy, leading to dose reductions, treatment delays, and high rates of early death and treatment-related mortality. Some reports indicate that pediatric-inspired chemotherapy protocols can be safely and efficiently used in older adults, resulting in improved median overall survival (mOS) ranging from 17 to 40 months. Despite such reports, front-line implementation of pediatric-inspired approaches to elderly patients with ALL remains a topic of discussion. Our goal is to estimate OS and define adverse events (AEs) in patients with ALL, aged > 60 years, and treated with a pediatric-inspired protocol. Methods All newly diagnosed patients aged > 60 years with Ph-negative ALL who received induction chemotherapy with a modified, asparaginase-intense, pediatric-inspired regimen between January 2002 and January 2022 were included. The treatment regimen consisted of induction, central nervous system prophylaxis, 7 cycles of intensification, and 24 cycles of maintenance. During these 20 years, we switched from native to pegylated E.coli asparaginase. Standard descriptive statistics were used to summarize patients’ demographics and outcomes of interest. 95% confidence intervals were provided where possible. Fisher's exact test was used to assess the impact of categorical covariates of interest on induction mortality. Using Fine-Gray methods, the Multivariable Cox proportional hazards regression model was used to determine the joint effect of potential factors for outcomes. P<0.05 was considered significant. Results A total of 76 patients were included. Patient and disease characteristics are presented in table 1. The median dose of Peg-asparaginase and L- asparaginase were 935 iu/m2 (477-1,111 iu/m2) and 5,944 iu/m2 (4,388-15,000 iu/m2) respectively. AEs rates found were severe pancreatitis 3.9%, thrombosis at any time during treatment 43.2%, hypofibrinogenemia <1g/L 30.6%, CTCAE grade IV transaminases, and total bilirubin 35.2%, and 17.3% respectively. The induction mortality rate was 12% (N=9) and the complete remission rate after induction (CR1) was achieved at 79% (n=60). Allogeneic hematopoietic stem cell transplantation in CR1 was carried out for 9.2% (N=7). The median follow-up among survivors was 49.7 months (range: 9-155) and the mOS was 35.1 months (95%CI: >19.3) (figure 1). OS rate at 1 and 4 years was 73.6% (95%CI: 62 - 82) and 42.2% (95%CI: 29.3 - 54.6) respectively, with a cumulative incidence of relapse from the date of diagnosis at 12 months of 12% (95% CI: 5.8 - 20). Leukemia-free survival rate at 4 years was 42.4% (95% IC 30 - 53). For the patients with early mortality, 5 patients had L-asparaginase, 3 patients had no asparaginase, and one Peg-asparaginase (11.11%). In contrast, in the no early mortality group, 46 (68.6%) patients received L-asparaginase, 2 (2.9%) patients had no asparaginase, and 19 (28.3%) patients received Peg-asparaginase (p=0.011). In univariate analysis, variables significantly associated with worse OS were: older age [<70 years old (n=46) median OS 70.8 months (95%CI >31.1) vs >70 years old (n=30)14.4 months (95%CI 9.2-54.2) (p=0.016)], higher WBC count [<11x10e9/L (n=54) median OS was 70 months (95%CI 27-NA), while in those with WBC >11x10e9/L (n=22) was 17.2 months (95%IC 6-31) (p= 0.004)], and no asparaginase given [OS at 12 months was: 85% (95%CI 60.4 -94.9) in patients treated with Peg-asparaginase; 72.4% (95%CI 57.9-82.6) in patients treated with L-asparaginase, and 40% (95%CI 5.2-75.3) in patients that did not receive asparaginase (p=0.0021). In multivariable analysis, younger age and lower WBC remained independent significant prognostic factors for increased OS [Patients <70 years old HR 2.67 (95% CI[1.38 - 5.17], p=0.0034) and patients with WBC <11x10e9/L HR 2.5 (95% CI [1.30- 4.82], p= 0.007)]. Conclusions The use of a pediatric-inspired chemotherapy protocol is shown to be effective and well tolerated in patients with Ph-negative ALL aged >60 years. Although AE rates were not negligible, outcomes were excellent and, early mortality improved over prior reports (Marc Poch Martell et al, BJH 2013, early mortality 20%). Further research will be needed to understand how the outcomes could be improved further using newer targeted treatments. Figure 1View largeDownload PPTFigure 1View largeDownload PPT Close modal

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)0.002
metaresearch head score (Gemma)0.006
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 score0.012

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.006
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0000.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

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 head0.262
Teacher spread0.253 · 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".

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Published2022
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