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G-CSF Slashes Irinotecan-Related Neutropenia and Diarrhea

February 1, 1999
Publication
Article
Oncology NEWS InternationalOncology NEWS International Vol 8 No 2
Volume 8
Issue 2

ATHENS-Early results from a phase III multicenter study suggest that the major dose-limiting side effects of irinotecan (Camptosar) in colon cancer-neutropenia and delayed diarrhea developing 24 hours after administration-can be controlled by the use of G-CSF (Neupogen).

ATHENS—Early results from a phase III multicenter study suggest that the major dose-limiting side effects of irinotecan (Camptosar) in colon cancer—neutropenia and delayed diarrhea developing 24 hours after administration—can be controlled by the use of G-CSF (Neupogen).

This preliminary analysis, presented at the European Society for Medical Oncology Congress, was based on data from 361 patients, two-thirds of whom had liver metastases and 80% of whom had received prior chemotherapy. Study participants were randomized to receive irinotecan, 350 mg/m² as a 30-minute IV infusion every 3 weeks, followed by 9 days of treatment with G-CSF, 150 g/m²/day, or irinotecan alone.

G-CSF treatment halved the incidence of grade 3-4 neutropenia and delayed diarrhea, as well as the incidence of concomitant severe neutropenia and diarrhea, reported investigator Paris Kosmidis, MD, of Hygeia Hospital, Athens. As a result, Dr. Kosmidis said, patients receiving growth factor were able to receive more of their chemotherapy courses on time. The relative dose intensity achieved, the rate of discontinuation due to adverse effects, and the frequency of febrile episodes were similar in both groups, however.

Irinotecan produced responses in 10% of patients and stabilized disease progression in more than half. “This is consistent with literature results for heavily pretreated patients with extensive disease,” he said. When irinotecan is combined with G-CSF, he said, “it seems there are fewer side effects, better quality of life, and less risk of severe dehydration.” Still to be explored are cost effectiveness of G-CSF and possible impact on survival.

Articles in this issue

Paclitaxel Plus Mitoxantrone for Poor-Prognosis Breast Cancer
Overview Shows Raloxifene Reduces Breast Cancer Incidence in Postmenopausal Women
Faslodex, Pure Antiestrogen, Studied in Tamoxifen-Resistant Breast Cancer
LHRH Agonist Plus Tamoxifen Improves Outcome in Young Metastatic Patients
Pros and Cons of Different Approaches to Chemoradiation
Less Cardiotoxicity With Liposomal Doxorubicin
Optimizing Docetaxel Tolerability in Anthracycline-Resistant Breast Cancer
Doxorubicin Appears to Change Natural History of HER-2+ Cancer’s
Tamoxifen After Surgery/RT Decreases Local Recurrence Risk in DCIS Patients
Single-Agent Herceptin Effective as First-Line Treatment of Metastatic Breast Cancer
Dose-Intensive Chemo Improves Disease-Free Survival in High-Risk Cancer
Opportunities and Challenges Mark New Era of Adjuvant Breast Cancer Therapy
Toremifene Appears Equivalent to Tamoxifen as Adjuvant Therapy for Breast Cancer: Interim Analysis
Combining Conventional and Biologic Therapies
Paclitaxel-Doxorubicin Effective as Neoadjuvant Chemotherapy

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