Real-world evidence evaluation of the safety and efficacy of intensive chemotherapy with or without gemtuzumab ozogamicin (GO) in patients with newly diagnosed Acute Myeloid Leukemia (AML) and favorable or intermediate risk cytogenetics
Bibliographic record
Abstract
Abstract Introduction Gemtuzumab ozogamicin (GO) is approved for use in combination with cytarabine plus daunorubicin (7+3) for the treatment of de novo acute myeloid leukemia (AML) with favorable or intermediate risk cytogenetics. This study aimed to describe real-world evidence comparing the safety and efficacy of 7+3 alone or with GO in patients (pts) with AML. Patients and methods This retrospective study included adult pts with AML and favorable/intermediate risk cytogenetics who received 7+3 induction alone or with GO at the Princess Margaret Cancer Center (Toronto) from October 1st 2018 to October 1st 2024. GO was dosed at 3 mg/m2 on days 1, 4 and 7 with 7+3 per the ALFA-0701 protocol. Endpoints included composite complete remission (CRc) rates, measurable residual disease (MRD) negativity rates, overall survival (OS) and relapse-free survival (RFS) with analysis of key genetic subgroups (core binding factor [CBF], NPM1-mutated [NPM1mut], intermediate-risk cytogenetics without NPM1mut [INT]). Propensity score matching with inverse probability treatment weighting (IPTW) compared outcomes with 7+3 vs 7+3+GO, matching for age, sex, ECOG, WBC, NPM1mut and CBF-AML. Veno-occlusive disease (VOD), bleeding, and hepatotoxicity were adverse events (AEs) evaluated with severity graded by CTCAE v5.0. Results In total, 162 pts were included, 62 received 7+3+GO and 100 received 7+3. Median age was 58 years (range, 22-85), 51% were male, 85% had ECOG of 0-1 and median WBC was 9.0 x 109/L (range, 0.5 – 288.0), with no differences between groups. Twenty-six (42%) pts who received 7+3+GO had CBF AML (15 [24%] t(8;21), 11 [18%] inv(16)), vs 10 (10%) pts who received 7+3 (3 [3%] t(8;21), 7 [7%] inv(16)) (p<0.05). Twenty-eight (45%) pts who received 7+3+GO had intermediate-risk cytogenetics vs 81 (81%) pts who received 7+3 (p<0.05), including 14 (23%) and 45 (45%), respectively, without NPM1mut (INT). In pts who received 7+3+GO, 17 (27%) had NPM1mut AML vs 41 (41%) in pts who received 7+3 (p=0.20). CRc was achieved in 56 (90%) pts with 7+3+GO and in 77 (77%) pts with 7+3 (p<0.05). CRc rates were similar within each genetic subgroup: 96% vs 100% (CBF); 88% vs 90% (NPM1mut); and 57% vs 51% (INT) for pts who received 7+3+GO vs 7+3, respectively. MRD negativity by flow cytometry was achieved in 46 (81%) vs 58 (58%) in pts after 7+3+GO and 7+3, respectively (p<0.05). MRD negativity rates were not significantly different within each genetic subgroups: 92% vs 80% (CBF, p=0.30); 65% vs 73% (NPM1mut, p=0.54); and 57% vs 42% (INT, p=0.54) for pts who received 7+3+GO vs 7+3, respectively. With a median follow-up of 28.6 months (7+3+GO) and 44.1 months (7+3), the 2-year OS was 78% (95% CI, 68-90) and 64% (95% CI, 55-75), respectively, (HR, 0.71, 95% CI 0.38-1.33, p=0.29). In pts with inv(16) AML, the 2-year OS was 91% (95% CI, 75-100) with 7+3+GO and 86% (95% CI, 63-100) with 7+3 (p=0.87). In pts with t(8;21) AML, the 2-year OS was 66% with 7+3+GO and 3/3 pts with 7+3 were alive at last follow-up. In pts with INT AML, the 2-year OS was 78% (95% CI, 59-100) with 7+3+GO vs 58% (95% CI, 44-76) with 7+3 (p=0.40). In pts with NPM1mut AML, the 2-year OS was 74% (95% CI, 54-100) with 7+3+GO and 70% (95% CI, 57-86) with 7+3 (p=1.00). Among patients achieving CRc, the 2-year RFS was 68% (95% CI, 56-83) with 7+3+GO and 65% (95% CI, 55-77) with 7+3 (p=1.00). There were no significant differences in 2-year RFS between pts who received GO or not within each pre-specified subgroup. The frequency of AEs was higher in pts treated with 7+3+GO: VOD 4 (6%) vs 0 (0%); grade 3-4 AST/ALT elevation 9 (15%) vs 10 (10%); and grade 3-4 bleeding 15 (24%) vs 11 (11%). Grade 5 bleeding was reported in 3 (5%) and 1 (1%) pts, respectively. The 60-day mortality rate was 7% both with 7+3+GO and with 7+3 (p=1.00). With propensity score matching with IPTW, 2-year OS was 81% (95% CI, 71-92) with 7+3+GO and 68% (95% CI, 59-79) with 7+3 (p=0.39), (HR 0.73, 95% CI 0.36-1.5, p=0.39). The 2-year RFS was 73% (95% CI, 60-87) and 69% (CI 95%, 58-81) with 7+3+GO and 7+3, respectively. Conclusion Within key subgroups of AML (CBF, NPM1mut and INT), the use of GO did not result in significant improvements in CRc, MRD negativity rates and survival outcomes in this retrospective study. VOD, liver enzymes elevation, and bleeding were more frequent with GO. Further research, including larger sample size is needed to identify pts who benefit from GO and to optimize clinical outcomes.
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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 | 0.020 | 0.046 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.002 | 0.006 |
| Bibliometrics | 0.001 | 0.002 |
| Science and technology studies | 0.000 | 0.001 |
| Scholarly communication | 0.002 | 0.001 |
| Open science | 0.001 | 0.001 |
| Research integrity | 0.001 | 0.001 |
| Insufficient payload (model declined to judge) | 0.003 | 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".