A phase II trial of mesna/ifosfamide, mitoxantrone and etoposide for refractory lymphomas

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Abstract

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 21-28 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. © 1994 Kluwer Academic Publishers.

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Rodriguez, M. A., Cabanillas, F. C., Hagemeister, F. B., Mclaughlin, P., Romaguera, J. E., Swan, F., & Velasquez, W. (1995). A phase II trial of mesna/ifosfamide, mitoxantrone and etoposide for refractory lymphomas. Annals of Oncology, 6(6), 609–612. https://doi.org/10.1093/oxfordjournals.annonc.a059252

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