Annals of Oncology 6:609-612, 1995
© 1995 European Society for Medical Oncology
brief-report |
A phase II trial of mesna/ifosfamide, mitoxantrone and etoposide for refractory lymphomas
Department of Hematology, The University of Texas M.D. Anderson Cancer Center Houston, TX, U.S.A.
Correspondence to: M. Alma Rodriguez, M.D. U.T. M.D. Anderson Cancer Center, 1515 Holcombe Blvd., Box 68, Houston, TX 77030, USA.
BACKGROUND: We have previously reported that combination chemotherapy based on the drugs cytarabine/platinum is effective in recurring lymphomas. In this phase II study, we prospectively studied a combination regimen of mesna/ifosfamide, mitoxantrone and etoposide (MINE) in patients with recurring lymphoma who had already received cytarabine/ platinum but did not respond to the treatment.
PATIENTS AND METHODS: 48 patients received MINE at the following doses: mesna 1.33 g/m2 IV daily x3, and 500 mg p.o. daily 4 hours after each IV dose; ifosfamide 1.33 g/m2 IV daily, given concurrently with mesna, x3 d; mitoxantrone 8 mg/m2 IV on day 1; and etoposide 65 mg/m2 IV daily x3. Treatment cycles were 2128 days apart, depending on patients' blood counts, with a maximum number of 6 cycles in responding patients. The histologic grade of the lymphomas according to the Working Formulation was low in 8 patients and intermediate in 40 patients. In the latter group, 12 were transformed from low grade.
RESULTS: Overall, 48% of the patients responded, with 21% having a complete response (CR), and 27% having a partial response (PR). The median survival time was 9 months, and the median follow-up of survivors is 51 months at this writing. Median time to treatment failure was 12 months for patients with complete responses, and 5 months for patients with partial responses. The most serious complication was myelosuppression, with 2 deaths resulting from neutropenic infection.
CONCLUSION: The MINE regimen induced responses in a moderate fraction of patients after their prior exposure to cytarabine/platinum salvage therapy, indicating there is no absolute cross resistance between these drug regimens.
ifosfamide, salvage therapy, lymphoma
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