High‐dose cyclophosphamide without stem cell transplantation in systemic lupus erythematosus
Authors:
- 10 January 2003
- journal article
- clinical trial
- Published by Wiley in Arthritis & Rheumatism
- Vol. 48 (1) , 166-173
Abstract
Objective: High‐dose chemotherapy followed by hematopoietic stem cell transplantation is increasingly being studied as a treatment for severe autoimmune disorders, such as systemic lupus erythematosus (SLE). High‐dose cyclophosphamide, the foundation of virtually all conditioning regimens for stem cell transplantation, is not myeloablative; therefore, when high‐dose cyclophosphamide is used alone, autografting, with its potential for reinfusing autoreactive effector cells, is not required. We undertook this study to investigate the safety and efficacy of high‐dose cyclophosphamide without stem cell transplantation in refractory SLE.Methods: We treated 14 patients with moderate‐to‐severe SLE that had been refractory to corticosteroids and one or more additional immunosuppressive drugs. All patients received 50 mg/kg of cyclophosphamide for 4 consecutive days followed by 5 μg/kg granulocyte colony‐stimulating factor until the neutrophil count was 1 × 109/liter for 2 consecutive days. Patients were followed up monthly for disease activity using the physician's global assessment, SLE Disease Activity Index, and assessment of functioning of involved organs. The Responder Index for Lupus Erythematosus was used to define partial or complete response.Results: The median time to achieve a neutrophil count of 0.5 × 109/liter was 14 days (range 11–22 days) after the last dose of cyclophosphamide. Patients required a median of 2 units (range 2–5) of packed red blood cells, and a median of 16 days (range 0–23 days) elapsed from the last dose of cyclophosphamide to the last platelet transfusion. There were no deaths or fungal infections. Significant improvements in physician's global assessment (mean difference 1.4; P < 0.0001), SLE Disease Activity Index (mean difference 4.1; P = 0.0039), and prednisone dosage (mean difference 14.9 mg/day; P = 0.002) were observed. Responses, including 5 durable complete responses, were observed in all organ systems (renal, central nervous system, and skin) with involvement that had led to patient enrollment.Conclusion: High‐dose cyclophosphamide without stem cell transplantation leads to rapid hematopoietic reconstitution and has significant clinical benefit in patients with refractory SLE. Therefore, this approach deserves further study.Keywords
This publication has 22 references indexed in Scilit:
- Durable Treatment-Free Remission after High-Dose Cyclophosphamide Therapy for Previously Untreated Severe Aplastic AnemiaAnnals of Internal Medicine, 2001
- Increased cervical dysplasia in intravenous cyclophosphamidetreated patients with SLE: a preliminary studyLupus, 2000
- Methylprednisolone and Cyclophosphamide, Alone or in Combination, in Patients with Lupus NephritisAnnals of Internal Medicine, 1996
- Lupus nephritisCurrent Opinion in Rheumatology, 1996
- Risk for Sustained Amenorrhea in Patients with Systemic Lupus Erythematosus Receiving Intermittent Pulse Cyclophosphamide TherapyAnnals of Internal Medicine, 1993
- Derivation of the sledai. A disease activity index for lupus patientsArthritis & Rheumatism, 1992
- Clinical and Immunologic Effects of Monthly Administration of Intravenous Cyclophosphamide in Severe Systemic Lupus ErythematosusNew England Journal of Medicine, 1988
- 4-Hydroperoxycyclophosphamide inhibits proliferation by human granulocytemacrophage colony-forming cells (GM-CFC) but spares more primitive progenitor cellsLeukemia Research, 1985
- The 1982 revised criteria for the classification of systemic lupus erythematosusArthritis & Rheumatism, 1982
- Treatment of ongoing experimental myasthenia gravis with short term high dose cyclophosphamideMuscle & Nerve, 1982