Chemotherapy-induced neutropenia with FOLFOX in the adjuvant treatment of colorectal cancer.
Bibliographic record
Abstract
38 Background: Patients undergoing adjuvant treatment with FOLFOX for colorectal cancer (CRC) are at risk of developing chemotherapy-induced neutropenia (CIN). We assessed the risk of CIN and the use of granulocyte colony stimulating factor (GCSF). Methods: We performed a retrospective chart review of patients with CRC treated with FOLFOX at our institution from 2013 - 2015. Demographic and treatment data were collected. CIN was defined as ANC <1.5, and all episodes of neutropenia were assumed to be the result of chemotherapy. Results: A total of 302 patients were included (baseline demographics in Table). In the overall cohort, 174 (58%) of patients had at least 1 episode of CIN. The risk CIN was 47% in stage II, 60% in low risk stage III (T1-3 and N1), and 58% in high risk stage III (T4 or N2). Among patients with at least 1 episode of CIN, the 1st CIN event occurred during the 1st 3 months of treatment in 76%, and the median cycle of 1st occurrence was 4 (95% CI 4-5), which did not differ by stage. Among patients who had at least 1 episode of CIN, 112 (64%) had a 2nd episode at a median cycle of 9 (95% CI 8-10). Among patients with at least 1 episode of CIN, 79 (45%) received subsequent GCSF, initiated 1 cycle after the 1st CIN event 37% of the time. Among patients with at least 2 episodes of CIN (n=112), 58 (52%) received GCSF after the 1st or 2nd event. Of these, 40 patients (69%) started GCSF newly after the 2nd CIN event. Among patients starting GCSF after the 2nd CIN event, 47% initiated GCSF 1 cycle later. The median cycle at which the relative dose intensity of FOLFOX decreased to <85% was cycle 6 (95% CI 5-8) in those with no CIN events, cycle 3 (95% CI 2-4) in those with at least 1 CIN event treated with GCSF, and cycle 5 (95% CI 4-6) in those with at least 1 CIN event treated without GCSF. Conclusions: CIN is a frequent occurrence during the adjuvant treatment of CRC with FOLFOX and most often occurs in the first 3 months of treatment. While oncologists may treat some patients with 3 months of FOLFOX rather than 6, physicians must be aware of CIN regardless of the planned duration of treatment. Early initiation of GCSF may be a consideration. [Table: see text]
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How this classification was reachedexpand
Full frame distilled prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.
Codex and Gemma teacher scores by category
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.000 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.001 | 0.000 |
| Bibliometrics | 0.000 | 0.000 |
| Science and technology studies | 0.000 | 0.000 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.000 | 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 teacher head, 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".