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Eloxatin
Clinical Pharmacology
Eloxatin
The length of a treatment cycle was 2 weeks for the ELOXATIN and 5-FU/LV regimen; 6 weeks for the irinotecan plus 5-FU/LV regimen; and 3 weeks for the ELOXATIN plus irinotecan regimen. The median number of cycles administered per patient was 10 (23.9 weeks) for the ELOXATIN and 5-FU/LV regimen, 4 (23.6 weeks) for the irinotecan plus 5-FU/LV regimen, and 7 (21.0 weeks) for the ELOXATIN plus irinotecan regimen. Patients treated with the ELOXATIN and 5-FU/LV combination had a significantly longer time to tumor progression based on investigator assessment, longer overall survival, and a significantly higher confirmed response rate based on investigator assessment compared to patients given irinotecan plus 5-FU/LV. The following table summarizes the efficacy results.
Table 21 – Summary of Efficacy
| ELOXATIN + 5-FU/LV N=267 |
irinotecan + 5-FU/LV N=264 |
ELOXATIN + irinotecan N=264 |
|
| Survival (ITT) | |||
| Number of deaths N (%) | 155 (58.1) | 192 (72.7) | 175 (66.3) |
| Median survival (months) | 19.4 | 14.6 | 17.6 |
| Hazard Ratio and (95% confidence interval) | 0.65 (0.53-0.80)* | ||
| P-value | < 0.0001* | - | - |
| TTP (ITT, investigator assessment) | |||
| Percentage of progressors | 82.8 | 81.8 | 89.4 |
| Median TTP (months) | 8.7 | 6.9 | 6.5 |
| Hazard Ratio and (95% confidence interval) | 0.74 (0.61-0.89)* | ||
| P-value | 0.0014* | - | - |
| Response Rate (investigator assessment)** | |||
| Patients with measurabledisease | 210 | 212 | 215 |
| Complete response N (%) | 13 (6.2) | 5 (2.4) | 7 (3.3) |
| Partial response N (%) | 82 (39.0) | 64 (30.2) | 67 (31.2) |
| Complete and partial response N (%) | 95 (45.2) | 69 (32.5) | 74 (34.4) |
| 95% confidence interval | (38.5 – 52.0) | (26.2 – 38.9) | (28.1 – 40.8) |
| P-value | 0.0080* | - | - |
| *Compared to irinotecan plus 5-FU/LV (IFL)
arm **Based on all patients with measurable disease at baseline |
|||
The numbers in the response rate and TTP analysis are based on unblinded investigator assessment.
Figure 4 illustrates the Kaplan-Meier survival curves for the comparison of ELOXATIN and 5-FU/LV combination and ELOXATIN plus irinotecan to irinotecan plus 5-FU/LV.
Figure 4 – Kaplan-Meier Overall Survival by treatment arm
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A descriptive subgroup analysis demonstrated that the improvement in survival for ELOXATIN plus 5-FU/LV compared to irinotecan plus 5-FU/LV appeared to be maintained across age groups, prior adjuvant therapy, and number of organs involved. An estimated survival advantage in ELOXATIN plus 5-FU/LV versus irinotecan plus 5-FU/LV was seen in both genders; however it was greater among women than men. Insufficient subgroup sizes prevented analysis by race.
Combination Therapy with ELOXATIN and 5-FU/LV in Previously Treated Patients with Advanced Colorectal Cancer
Generic Name: Oxaliplatin Injection
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