ESHAP as salvage therapy for refractory non-Hodgkin's lymphoma: Taiwan experience

Citation
Ws. Wang et al., ESHAP as salvage therapy for refractory non-Hodgkin's lymphoma: Taiwan experience, JPN J CLIN, 29(1), 1999, pp. 33-37
Citations number
16
Categorie Soggetti
Oncology
Journal title
JAPANESE JOURNAL OF CLINICAL ONCOLOGY
ISSN journal
03682811 → ACNP
Volume
29
Issue
1
Year of publication
1999
Pages
33 - 37
Database
ISI
SICI code
0368-2811(199901)29:1<33:EASTFR>2.0.ZU;2-Q
Abstract
Background: The ESHAP regimen, a combination of the chemotherapeutic drugs etoposide, methylprednisolone (solumedrol), high-dose cytarabine (ara-C) an d cisplatin, has been shown to be active against refractory non-Hodgkin's l ymphoma in therapeutic trials. We were interested in determining whether th is regimen would be effective and tolerable for Chinese patients. Methods: Thirty-two patients with refractory/relapsed non-Hodgkin's lymphom a (23 intermediate-grade and nine high-grade) were enrolled in this study. Etoposide was administered at a dose of 40 mg/m(2)/day as a 1 h intravenous infusion from day 1 to day 4, solumedrol 500 mg/day was given as a 15 min intravenous infusion from day 1 to day 5, ara-C 2 g/m(2) was given as a 2 h intravenous infusion on day 5 and cisplatin was given at a dose of 25 mg/m (2)/day as a continuous infusion from day 1 to day 4. Clinical efficacy and toxicity were assessed on the basis of the WHO criteria. Results: Ten patients (31.3%, 95% CI 15.2-47.4%) attained complete remissio n (CR) and seven had partial remission (PR). The overall response rate was 53.1% (95% CI 35.8-70.4%). In eight of the 10 CR patients, the remission la sted for more than 8 months. The remaining two patients had CR of 5 and 6 m onths. The median duration of CR was 12.2 months (range 5-22 months). Myelo suppression with subsequent infections was the major toxicity. Severe leuko penia (WBC <1000/mu l) lasted for an average of 12 days and thrombocytopeni a (<25 000/mu l) 18 days. One patient (3.1%) died of neutropenia-associated sepsis within 4 weeks after treatment. Non-myeloid toxicities included alo pecia in 66% (28% grade 2, 22% grade 3), stomatitis in 72% (25% grade 2, 28 % grade 3, 13% grade 4), hepatotoxicity in 9% (3% grade 2), renal toxicity in 13% (6% grade 2, 3% grade 3) and infection in 56% (18% grade 2, 25% grad e 3, 13% grade 4). The majority of the responders relapsed within 2 years a fter ESHAP treatment. Median survival for all patients was 8.6 months. Conclusions: ESHAP is an active and tolerable regimen in Chinese patients w ith relapsed/refractory lymphoma, but the duration of remission is brief an d without significant impact on survival.