Chemoradiation or standard radiation followed by adjuvant temozolomide (TMZ) and 13-cis-retinoic acid (CRA) for high grade glioma in adults - a regional cancer centre study
Bibliographic record
Abstract
1557 Background: A recent phase II study reported activity of TMZ and cRA for recurrent/progressive malignant gliomas with 43% 6 month progression-free survival (PFS); 32% for glioblastoma multiforme (GBM) patients (Jaeckle KA et al, 2003). Methods: From 2000–2003, we retrospectively analyzed adults with malignant glioma who received, following surgery and radiation therapy (RT) ± low dose TMZ (75 mg/m2/d x 42d), TMZ (150–200mg/m2/d, d1–5) and cRA (100 mg/m2/d, d1–21) every 28d for up to 24 cycles or until progression on neuroimaging. Time to progression (TTP) was the primary end-point and overall survival (OS) was the secondary end-point. Results: Of 33 patients (29 GBM, 2 anaplastic astrocytoma, AA, 2 malignant glioma, MG), 18 remain alive. The 33 patients received 308 cycles of TMZ/cRA (mean 9.3 cycles); 9 patients received greater than 10 cycles, but only 2 completed more than 15 cycles. Responses to TMZ/cRA were documented in 15/33 (45%) patients (10 partial responses/5 stable disease). For all patients, median TTP was 38.6 weeks, 50.5 weeks for chemoradiation patients and 27.1 weeks for those who received RT alone prior to TMZ/cRA, NS). Median OS was 103.2 for all 33 patients, 55.3 weeks for RT alone and median time not yet reached for RT/low dose TMZ, p=0.01). 6, 12 and 24 month TTP was 63%/39%/39% (53%/27%/27% for RT alone and 72%/49%/49% for RT/low dose TMZ). OS at 6, 12 and 24 months was 94%, 69% and 43%, respectively, for all 33 patients (86%/50%/25% for RT alone and 100%/86%/75% for RT/low dose TMZ). Conclusions: Our data for malignant glioma patients who received concurrent low dose temozolomide with RT prior to adjuvant temozolomide/cRA compares favourably with the results of the recently completed EORTC/NCIC trial (Stupp R et al, ASCO 2004). The chemoradiation strategy using concurrent low dose temozolomide provides a significant survival advantage when compared to radiation alone. Our study demonstrates that TMZ/cRA prolongs TTP for patients with malignant gliomas when compared to historical controls and supports use of this regimen in a Phase III clinical trial. No significant financial relationships to disclose.
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How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot 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.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.001 | 0.001 |
| Meta-epidemiology (narrow) | 0.001 | 0.000 |
| Meta-epidemiology (broad) | 0.001 | 0.001 |
| Bibliometrics | 0.000 | 0.001 |
| Science and technology studies | 0.000 | 0.000 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.001 | 0.000 |
| Research integrity | 0.000 | 0.001 |
| Insufficient payload (model declined to judge) | 0.002 | 0.000 |
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.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
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".