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On-line version ISSN 1414-431X
Braz J Med Biol Res vol.33 n.7 Ribeirão Preto July 2000
Braz J Med Biol Res, July 2000, Volume 33(7) 791-798
Amifostine (WR-2721), a cytoprotective agent during high-dose cyclophosphamide treatment of non-Hodgkin's lymphomas: a phase II study
1Centro de Hematologia e Hemoterapia, Unidade de Transplante de Medula, Universidade Estadual de Campinas, Campinas, SP, Brasil
2Department of Hematology, San Martino Hospital, Genoa, Italy
Patients and Methods
Correspondence and Footnotes
Clinical trials indicate that amifostine may confer protection on various normal tissues without attenuating anti-tumor response. When administered prior to chemotherapy or radiotherapy, it may provide a broad spectrum of cytoprotection including against alkylating drugs. The mechanism of protection resides in the metabolism at normal tissue site by membrane-bound alkaline phosphatase. Toxicity of this drug is moderate with hypotension, nausea and vomiting, and hypocalcemia being observed. We report a phase II study using amifostine as a protective drug against high-dose cyclophosphamide (HDCY) (7 g/m2), used to mobilize peripheral blood progenitor cells (PBPC) and to reduce tumor burden. We enrolled 29 patients, 22 (75.9%) affected by aggressive and 7 (24.1%) by indolent non-Hodgkin's lymphoma (NHL), who were submitted to 58 infusions of amifostine and compared them with a historical group (33 patients) affected by aggressive NHL and treated with VACOP-B followed by HDCY. The most important results in favor of amifostine were the reduction of intensity of cardiac, pulmonary and hepatic toxicity, and a significant reduction of frequency and severity of mucositis (P = 0.04). None of the 29 patients died in the protected group, while in the historical group 2/33 patients died because of cardiac or pulmonary toxicity and 2 patients stopped therapy due to toxicity. Amifostine did not prevent the aplastic phase following HDCY. PBPC collection and hematological recovery were adequate in both groups. The number of CFU-GM (colony-forming units-granulocyte/macrophage) colonies and mononuclear cells in the apheresis products was significantly higher in the amifostine group (P = 0.02 and 0.01, respectively). Side effects were mild and easily controlled. We conclude that amifostine protection should be useful in HDCY to protect normal tissues, with acceptable side effects.
Key words: amifostine, cytoprotection, non-Hodgkin's lymphoma, high-dose cyclophosphamide, peripheral blood progenitor cell mobilization
The two major obstacles in an effective cancer therapy are drug resistance and toxicity to normal organs which prevent the use of optimal doses and schedules. A broad-spectrum selective cytoprotective agent which improves patient tolerance could allow the delivery of higher cumulative doses of chemotherapy and would improve life quality, a useful adjunct in cancer medicine.
Amifostine is a pro-drug that is dephosphorylated in the tissue by alkaline phosphatase to a free thiol, the active metabolite (WR-1065) (1-3). It acts as a potent scavenger of oxygen free radicals induced by ionising radiation and certain types of chemotherapy (1-3). The mechanism of protection is based on physiological differences between the two tissue types and on differential uptake of amifostine in normal and tumor tissue (4). Cytoprotection has been found to correlate only with intracellular levels of the thiol metabolite WR-1065 (2). Further reaction with other intracellular thiol groups forms either its symmetrical disulfide or mixed disulfides. The hydrogen atom donation from these metabolites facilitates direct chemical repair at sites of DNA damage. Amifostine selectively protects a broad range of normal tissues against the toxicity associated with chemotherapy and radiation without affecting the anti-tumor activity of the agents (3,5-7). Many experiments have demonstrated that there is no evidence of attenuation of the anti-tumor effect when amifostine protection is used (1,8,9). Pre-incubation with amifostine or WR-1065 enhanced the colony-forming capacity of the bone marrow progenitors, increasing recovery of CFU-GEMM (colony-forming units-granulocyte/erythroid/macrophage/mega-karyocytic) and BFU-E (burst-forming units-erythroid) up to seven-fold (1,10). Significant side effects related to amifostine include nausea, vomiting, and hypotension (1,11,12). An additional side effect is transient hypocalcemia because of inhibition of the release of parathyroid hormone (1,13). The most clinically significant and dose-limiting toxicity is hypotension generally at the end of the infusion and quickly reversible by discontinuation of the drug (1,11,12). The precise mechanism of hypotension is unclear but it seems to be related to a direct vasodilator (14).
In view of these considerations, we report here a phase II study using amifostine protection in patients treated with high-dose alkylating agent (cyclophosphamide (CY), 7 g/m2), in order to mobilize peripheral blood progenitor cells (PBPC) and to reduce the tumor mass in patients affected by non-Hodgkin's lymphomas (NHL). The objective of the present investigation was to study the feasibility, side effects, and the extent of tissue and organ protection by amifostine.
From February 1997 to June 1999, 29 patients (14 males and 15 females), median age 46 years (range 18-56), 22 (75.9%) affected by aggressive NHL and 7 (24.1%) by indolent NHL, were enrolled in the study. Seven of the 29 patients (24.1%) were in complete remission, 15 (51.8%) in partial remission, and 7 (24.1%) were non-responders. Twelve (41.3%) patients had previously received one line of chemotherapy; 11 (37.9%), two lines, and 6 (20.8%), three or more (median treatment, 2 chemotherapy lines; range 1-5). The 29 patients were submitted to a total of 58 CY infusions protected by amifostine during the progenitor cell mobilization procedure (15). The total CY dose (7 g/m2) was divided into 5 equal infusions (1.4 g/m2). Amifostine was infused 30 min before the first and 5th CY infusion, as shown in Table 1. Amifostine was infused for 15 min and CY was administered 15 min after the end of amifostine infusion. Urinary pH was determined before amifostine infusion and it had to be ³7.0. Patients presenting pH <7 were treated with sodium bicarbonate in order to achieve the ideal pH before infusion. Twenty-seven (93.1%) patients were protected with 740 mg/m2 amifostine twice, while only two (6.9%) patients received 910 mg/m2 in each of the two infusions. Echocardiography was used as the criterion for the procedure. Patients presenting ventricular ejection fraction below 60% did not undergo therapy and patients presenting limit values were submitted to scintigraphy prior to high-dose cyclophosphamide (HDCY).
We analyzed neutrophil and platelet recovery, median number and range of leukaphereses, total mononuclear cells, CD34+ cells and CFU-GM colonies obtained from leukapheresis products. CD34 cells were quantified using a modification of the method described by Sutherland et al. (16). In this modification, the CD14/FITC antibody was used instead of CD45 to exclude contamination with myeloid/monocytic cells of the CD34/PE-positive population defined as CD14 negative and presenting a low relative granularity or internal complexity. The in vitro colony-forming assay was performed by plating total unstimulated peripheral blood leukocytes obtained after red blood cell sedimentation in the presence of 33% Emagel, as described elsewhere (17). The total number of CD34+ cells (x 106/kg) and CFU-GM (x 104/kg) was determined by multiplying their frequency per ml by the total volume of cryopreserved cell suspension and dividing by body weight. We compared these results with a historical non-protected group consisting of 40 patients affected by aggressive NHL. Before receiving HDCY, these patients were treated with a median number of 8 courses of VACOP-B (18), and 33 patients underwent HDCY therapy followed by granulocyte colony-stimulating factor (G-CSF) in order to collect PBPC and reduce the tumor burden. Seven patients did not undergo HDCY due to early death or progression of the disease. Table 2 shows the patients' characteristics, and Table 1 shows the time schedule for HDCY administration.
Side effects related to amifostine and evaluation of toxicity
The most important short-term side effects of amifostine were the presence of nausea and/or vomiting, hypotension, hypocalcemia and flu-like symptoms. Blood pressure was determined each 5 min during amifostine infusion. The infusion was reduced when the systolic blood pressure decreased more than 10% or if it decreased >20 mmHg over a period of 5 min or if symptomatic hypotension was present. Serum calcium levels were determined before, during and after amifostine infusion and at 24-h intervals for 4 days. The side effects were treated using methylprednisolone and/or intravenous calcium injections. Thirteen patients were treated preventively with dexamethasone (20 mg, twice a day), intravenous calcium injection and glanisentron (3 mg, iv) about 90 min before amifostine infusion. HDCY toxicity was determined according to the World Health Organization (WHO). Informed consent was obtained from the patients according to institution regulations.
Analysis was based on data for the amifostine group versus the historical non-protected group. Our main objective was to compare the theoretical benefits of amifostine cytoprotection. All data were analyzed with descriptive statistical methods and the proportions of patients within each group of characteristics and outcome, including short-term side effects, were compared by the Fisher test. In addition, comparisons of the continuous variables were performed by the Mann-Whitney test, with the level of significance set at P<0.05.
The most important symptoms related to amifostine infusions were nausea and vomiting in 12/58 patients (20.6%), hypotension in 26/58 (44.8%), hypocalcemia in 4/58 (6.9%), and flu-like symptoms in 2/58 (3.5%). All symptoms were mild and easily controlled by the use of methylprednisolone (125 mg, iv) or calcium gluconate (100-300 mg, iv) when necessary. Twenty-three patients (79%) presented fever of undetermined origin which was controlled with antibiotics. One patient presented grade 1 mucositis, two patients presented line contamination by Staphylococcus aureus, controlled with vancomycin, and one patient died due to progressive disease. Two patients showed cardiac toxicity, grade 1 and grade 2, respectively. No severe toxicity (grades 3 and 4) was observed in liver, kidney or lung (Table 3). Regarding hypotension, Figure 1 shows a slight reduction in blood pressure (median reduction of about 7.5%), 15 to 30 min after the beginning of amifostine infusion. No infusions were stopped because of hypotension. Figure 2 shows a slight reduction in serum calcium 72 h after amifostine infusion (median reduction of about 6%). The median day for neutrophil counts above 0.5 x 109/l was the 12th (10th-18th), for counts >1.0 x 109/l it was the 13th (10th-19th), for platelets >20 x 109/l it was the 11th (9th-25th) and for platelets >50 x 109/l it was the 12th (9th-30th). The median number of aphereses was 2 (range 1-9), the median total mononuclear cell count was 8.26 x 108/kg (3.3-29.9), the median count of CD34+ cells was 12.35 x 106/kg (2.0-74.1), and the median number of CFU-GM colonies was 114.14 x 104/kg (27.7-680.0).
Forty patients with aggressive NHL were enrolled in the study and received a median of 8 cycles of VACOP-B as front line therapy. Seven patients did not undergo HDCY due to progression of the disease or early death. Thirty-three patients underwent HDCY without amifostine protection. Four patients did not undergo autologous bone marrow transplantation due to severe toxicity after HDCY. Two patients died, one due to cardiac failure and one due to pulmonary fibrosis. In addition, two patients had severe liver and kidney toxicity, grades 3 and 4, respectively. Table 3 shows the toxicity related to HDCY in this group. The median day for neutrophil counts above 0.5 x 109/l was the 10th (7th-17th), for counts >1.0 x 109/l it was the 10th (8th-21st), for platelets >20 x 109/l it was the 11th (7th-27th), and for platelets >50 x 109/l it was the 13th (8th-43th). Patients underwent leukapheresis on median day 12 (range 10-16). A median of 3 aphereses (range 1-7) was performed. The median number of harvested mononuclear cells was 6.10 x 108/kg (range 0.14-23.9), the median number of CD34+ cells was 17.08 x 106/kg (range 2.87-103.0), and the median number of CFU-GM colonies was 45.0 x 104/kg (range 1.16-681.0).
Comparison between two groups
Table 3 shows non-hematologic toxicity according to WHO grades in both groups analyzed and its statistical significance. Mucositis toxicity was more frequent in the non-protected group (P = 0.04). However, the most important clinical differences were observed in the severity of toxicity. In the historical group we observed severe cardiac, renal, hepatic and pulmonary toxicity, including two lethal cases. No differences in hematologic toxicity were observed between groups. Neutrophil recovery was faster in the historical group (P<0.001), while no difference was observed between groups in terms of platelet recovery. PBPC collections were similar in both groups in terms of CD34+ cell numbers. However, the number of CFU-GM colonies and mononuclear cells was significantly higher in the amifostine-protected group (P = 0.02 and P = 0.01, respectively). The median number of aphereses was 3 (1-9) in the historical group and 2 (1-7) in the amifostine group, showing a trend in favor of the amifostine group (P = 0.06). Table 4 shows the biological data concerning PBPC mobilization in both groups.
This phase II study using amifostine as a cytoprotective agent following an infusion of 7 g/m2 of cyclophosphamide indicates that amifostine and its free thiol derivative may confer protection on most tissues and organs against HDCY. Amifostine was able to prevent severe and lethal cardiac and pulmonary toxicity, and to reduce the frequency and severity of renal toxicity and mucositis. Many antineoplastic drugs have been studied using cytoprotective agents including the anthracyclines, daunorubicin and doxorubicin, the anthracenedione, mitoxanthrone, paclitaxel, diaziquone, cisplatin, and thiotepa (1). However, few studies have used high-dose alkylating drug protection in bone marrow transplantation and/or mobilization procedures (19). A one-way crossover phase II trial was conducted in order to evaluate the protective effect of amifostine against cyclophosphamide-induced hematologic toxicity (20). The patients received 1500 mg/m2 of CY alone, protected with 740 mg/m2 of amifostine. Amifostine significantly attenuated the neutrophil nadir (P<0.001) and reduced the duration of neutropenia grade 4 (P£0.016). However, the CY dosage was much lower than those used in our study, and organic toxicity was not evaluated. On the other hand, our study using 7 g/m2 CY did not present any advantage of hematologic protection in terms of hematologic recovery compared with the historical group. The number of CFU-GM and mononuclear cells, however, was significantly higher in spite of more chemotherapy cycles previously applied to most of the protected patients, suggesting amifostine protection of progenitor cells. In addition, we observed a trend in favor of the amifostine group in terms of number of aphereses, which was lower in the protected group (P = 0.06). An important difference in favor of amifostine protection was the reduction of severe non-hematologic toxicity, particularly renal, hepatic, pulmonary and cardiac toxicity. Besides, mucositis was observed only in one patient (grade 1) and no treatment-related death was observed in the protected group. The choice of the protective dosage of amifostine used in this study was defined previously (21,22), ranging from 740 to 910 mg/m2, and seems to be safe and to have low side effects. The side effects related to amifostine were mild and easily controlled. In 58 infusions, the most important side effects were nausea and vomiting, hypotension, and clinical and/or laboratory hypocalcemia. Nausea and vomiting should be treated with careful fluid balance monitoring, beginning before infusion and using anti-emetic medication prior to and in conjunction with amifostine. Hypotension may be controlled using hydration prior to amifostine infusion, maintaining patients in the supine position, and controlling their blood pressure every 5 min. Calcium level was the only parameter that needed daily control for four to five days after amifostine infusion.
The administration of amifostine as a cytoprotective drug against HDCY seems to be simple and to have an acceptable toxicity profile. There was no evidence of attenuation of the anti-tumor effects in many experiments performed (8,9). Careful patient selection, prophylactic therapy before amifostine and monitoring blood pressure during infusion can minimize some of the associated side effects. Further investigation of the cytoprotective effects of amifostine with high-dose alkylating chemotherapy, particularly HDCY in combination with growth factors, and its utility in the therapy and progenitor cell mobilization procedure is required to confirm the importance of this procedure for tissue and organ protection. Randomized trials, including cost-benefits analysis, are needed to demonstrate the clinical usefulness of amifostine in HDCY treatment.
1. List AF, Heaton R, Glinsmann-Gibson B & Capizzi RL (1996). Amifostine protects primitive hematopoietic progenitors against chemotherapy cytotoxicity. Seminars in Oncology, 23 (Suppl 8): 58-63. [ Links ]
2. Smoluk GD, Fahey RC, Calabro-Jones PM, Aguilera JA & Ward JF (1988). Radio-protection of cells in culture by WR-2721 and derivates: Form of the drug responsible for protection. Cancer Research, 48: 3641-3647. [ Links ]
3. Calabro-Jones PM, Agulera JA, Ward JF, Smoluk GD & Fahey RC (1988). Uptake of WR-2721 derivates by cells in culture: Identification of the transported form of the drug. Cancer Research, 48: 3634-3640. [ Links ]
4. Capizzi RL (1996). The preclinical basis for broad-spectrum selective cytoprotection of normal tissues from cytotoxic therapies by amifostine (Ethiol). European Journal of Cancer, 32 (Suppl 4): S5-S16. [ Links ]
5. Grdina DJ & Sigdestad CP (1989). Radiation protectors: The unexpected benefits. Drug, 20: 13-42. [ Links ]
6. Calabro-Jones PM, Fahey RC, Smoluk GD & Ward JF (1985). Alkaline phosphatase promotes radioprotection and accumulation of WR-1065 in V79-171 cells incubated in medium containing WR-2721. International Journal of Radiation Biology, 47: 23-27. [ Links ]
7. Schuchter LM & Glick JH (1993). The current status of WR-2721 (amifostine): A chemotherapy and radiation therapy protector. Biology Therapy Cancer Updates, 3: 1-10. [ Links ]
8. Yuhas JM, Spellman JM, Jordan SW, Pardini MC, Afzal SMJ & Culo F (1980). Treatment of tumors with the combination of WR-2721 and cisdichlorodiamineplatinum (II) or cyclophosphamide. British Journal of Cancer, 42: 574-585. [ Links ]
9. Yuhas JM (1980). A more general role for WR-2721 in cancer therapy. British Journal of Cancer, 41: 832-834. [ Links ]
10. Wasserman TH, Philips TL, Ross G & Kane LJ (1981). Differential protection against cytotoxic chemotherapeutic effects on bone marrow CFUs by WR-2721. Cancer Clinical Trials, 4: 3-6. [ Links ]
11. Bukowski RM (1996). Amifostine (Ethiol): Dosing, administration and patient management guidelines. European Journal of Cancer, 32A (Suppl 4): S46-S49. [ Links ]
12. Schuchter LM (1996). Guidelines for the administration of amifostine. Seminars in Oncology, 23 (Suppl 8): 40-43. [ Links ]
13. Glover DJ, Riley L & Carmichael K (1983). Hypocalcemia and inhibition of parathyroid hormone secretion after administration of WR-2721 (a radioprotective and chemoprotective agent). New England Journal of Medicine, 309: 1137-1141. [ Links ]
14. U.S. Bioscience (1992). A phase I study to determine whether Ethiol (WR-2721) is a vasodilator when infused into the brachial artery of healthy volunteers. ETH CLPH 1. [ Links ]
15. Gianni AM, Bregni M, Siena S, Brambilla C, Di Nicola M, Lombardi F, Gandola L, Tarella C, Pileri A, Ravagnani F, Valagussa P, Bonadonna G, Stern A, Magni M & Caracciolo D (1997). High-dose chemotherapy and autologous bone marrow transplantation compared with MACOP-B in aggressive B-cell lymphoma. New England Journal of Medicine, 336: 1290-1297. [ Links ]
16. Sutherland DR, Keating A, Nayar R, Anania S & Stewart AK (1994). Sensitive detection and enumeration of CD34+ cells in peripheral and cord blood by cytometry. Experimental Hematology, 22: 1003-1110. [ Links ]
17. Tarella C, Benedetti G, Caracciolo D, Castellino C, Cherasco C, Bondesan P, Omede P, Ruggieri D, Gianni M & Pileri A (1995). Both early and committed haematopoietic progenitors are more frequent in peripheral blood than in bone marrow during mobilization induced by high-dose chemotherapy + G-CSF. British Journal of Haematology, 91: 535-543. [ Links ]
18. O'Reilly SE, Hoskins P, Klimo P & Connors JM (1991). MACOP-B and VACOP-B in diffuse large cell lymphomas and MOPP/ABV in Hodgkin's disease. Annals of Oncology, 2 (Suppl 1): 17-23. [ Links ]
19. Schering-Plough International (1994). Ethiol (Amifostine) for the Prevention of Chemotherapy-Induced Toxicity [Product Monograph]. Schering-Plough International, Kenilworth, NJ, 37-44. [ Links ]
20. Glover DJ, Glick JH, Weiler C, Hurowitz S & Kligerman MM (1986). WR-2721 protects against the hematologic toxicity of cyclophosphamide: A controlled phase II trial. Journal of Clinical Oncology, 4: 584-588. [ Links ]
21. Glover DJ, Fox KR, Weiler C, Kligerman MM, Turrisi A & Glick JH (1988). Clinical trials of WR-2721 prior to alkylating agent chemotherapy and radiotherapy. Pharmacology and Therapeutics, 39: 3-7. [ Links ]
22. Adamson PC, Balis FM, Belasco JE, Lange B, Berg SL & Blaney SM (1995). A phase I trial of amifostine (WR-2721) and melphalan in children with refractory cancer. Cancer Research, 55: 4069-4072. [ Links ]
We thank Eliana C.M. Miranda for data management.
Address for correspondence: C.A. De Souza, Centro de Hematologia e Hemoterapia, Unidade de Transplante de Medula, UNICAMP, 13083-080 Campinas, SP, Brasil. Fax: +55-19-788-8750. E-mail: firstname.lastname@example.org
Publication supported by FAPESP. Received August 10, 1999. Accepted March 9, 2000.