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Record W4405049116 · doi:10.1182/blood-2024-198044

Outcomes of Patients with Primary Central Nervous System Lymphoma Treated with Matrix Followed By High-Dose Chemotherapy and Autologous Stem Cell Transplant - a Multicentre, Retrospective Study

2024· article· en· W4405049116 on OpenAlexaffabout
Adam Suleman, Michael Crump, Robert Kridel, Sita Bhella, Chloe Yang, Vishal Kukreti, S.R. Foley, Tom Kouroukis, Amaris Balitsky, John Kuruvilla, Abi Vijenthira, Gwynivere A Davies, Anca Prica

Bibliographic record

VenueBlood · 2024
Typearticle
Languageen
FieldMedicine
TopicCNS Lymphoma Diagnosis and Treatment
Canadian institutionsMcMaster UniversityJuravinski HospitalUniversity Health NetworkUniversity of TorontoHamilton Health SciencesPrincess Margaret Cancer Centre
Fundersnot available
KeywordsPrimary central nervous system lymphomaMedicineAutologous stem-cell transplantationStem cellChemotherapyLymphomaChemotherapy regimenCentral nervous systemOncologyRetrospective cohort studyInternal medicineSurgery

Abstract

fetched live from OpenAlex

Background: Methotrexate, cytarabine, thiotepa and rituximab (MATRix) followed by high-dose chemotherapy (HDC) with a thiotepa-containing regimen and autologous stem cell transplant (ASCT) has become standard in Canadian centers for treatment of primary central nervous system lymphoma (PCNSL). However, there remains variation in high-dose chemotherapy regimens used, including thiotepa dosing. In Ontario, Canada's most populous province, patients at Princess Margaret Cancer Centre (PM) until 2021 underwent conditioning with carmustine and thiotepa 10mg/kg divided over 2 days. In December 2021, the thiotepa dose in the conditioning regimen was increased to 20mg/kg divided over 2 days aligning with the IELSG32 trial. At Juravinski Hospital (JH), patients are treated with busulfan (9.6mg/kg over 3 days) and thiotepa 600mg/m2 over 2 days. In a 70kg patient, with 1.9m2 BSA this would result in a 50% reduced dose of thiotepa at PM prior to December 2021, and a 17% reduced dose of thiotepa if treated at JH, compared to PM from December 2021 onwards (the IELSG32 dosing). Aim: As it is not clear if differences in thiotepa dosing impact clinical outcomes, we aimed to assess overall survival (OS), progression-free survival (PFS) and transplant toxicities of patients treated with MATRix followed by three different HDC regimens and ASCT at 2 large transplant centres in Ontario, Canada. Methods: We performed a retrospective review of patients with PCNSL treated with MATRix followed by HDCT and ASCT from 2017-2022 at PM, and from 2017-2020 at JH. Patients were included if they were >18 years, treated with MATRix first-line or for relapsed/refractory disease, and underwent consolidation with ASCT. Data on stem cell collection, conditioning regimen, and transplant toxicities were collected. OS and PFS were calculated using Kaplan-Meier method, and Cox regression analysis was used to assess the impact of patient and treatment variables on outcomes. Results: At PM and JH, 52 patients were treated with MATRix followed by HDC and ASCT and were included: 18 at JH with busulfan and thiotepa 600mg/m2 over 2 days (Cohort 1), 23 at PM with carmustine and thiotepa 10mg/kg over 2 days (Cohort 2), and 11 at PMCC with carmustine and thiotepa 20mg/kg over 2 days (Cohort 3). Patients were followed for a median of 26 months, 41 months and 15 months, respectively. There were no differences between cohorts in age or use of MATRix as first-line therapy. Most patients achieved a complete response (CR) or partial response (PR) on pre-ASCT MRI (83% in cohort 1, 87% in cohort 2, 100% in cohort 3, p=0.592). One patient in cohort 1 and 1 in cohort 2 had progressive disease after MATRix requiring salvage chemotherapy prior to ASCT. The median number of CD34+ cells infused per kg was 4.7 in cohort 1, 3.45 in cohort 2, 6.04 in cohort 3, p=0.036. Patients in cohorts 1 and 3 had higher rates of febrile neutropenia compared to patients in cohort 2 (94.4% and 81.8% compared to 65.2%, p=0.014). Median days to neutrophil recovery and platelet count recovery were similar (p=0.292 and 0.226 respectively). CR after ASCT was achieved in 13/18 patients (72%) in cohort 1, 13/23 patients (57%) in cohort 2 and 8/11 patients (73%) in cohort 3, p=0.288. The 18-month OS was 94.4% in cohort 1, 94.7% in cohort 2 and 90.9% in cohort 3 (p=0.545). The 18-month PFS was 94.1% in cohort 1, 86.3% in cohort 2, and 90.0% in cohort 3 (p=0.790). Over a median follow up of 26 months (range 1-79), there were 8 deaths. Causes of death included progression of lymphoma in 5 patients, infectious complications in 2 (pneumocystis pneumonia and bacterial sepsis), and an unrelated cause in 1 patient. Results from a Cox proportional hazard model showed no impact of baseline demographic features (age, sex, CD34+ cell dose collected), or treatment-related factors (conditioning regimen, achieving CR prior to ASCT, achieving CR after ASCT) on OS or PFS. Conclusion: These data from 2 academic transplant centres shows outcomes with MATRix followed by HDC with a thiotepa-based regimen and ASCT for patients with PCNSL are encouraging. Acknowledging the limited sample size and non-randomized comparison, differences in conditioning regimens including the use of carmustine versus busulfan and thiotepa dosing do not appear to significantly impact outcomes.

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)0.001
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 score0.003
Threshold uncertainty score0.006

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0010.001
Open science0.0000.001
Research integrity0.0010.001
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 head0.003
GPT teacher head0.198
Teacher spread0.194 · 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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Citations0
Published2024
Admission routes2
Has abstractyes

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