Introduction: the evolving role of bisphosphonate therapy in multiple myeloma.

Bone disease is a hallmark of multiple myeloma (MM) and contributes to most of the debilitating morbidity associated with this disease. Bone lesions result not only from the direct deposits of MM cells within the bone, but also from the release of soluble factors by both the tumor and the microenvironment, resulting in the stimulation of osteoclast activity and bone resorption. The use of pharmacologic intervention with bisphosphonate therapy has resulted in a significant reduction in skeletally related events such as the occurrence of pathologic fractures, lytic lesions, bone pain, and hypercalcemia. In addition, their use has been recently shown to provide a survival benefit in a subset of MM patients. In this issue of Blood, Kunzmann et al1 reveal a novel antitumor effect of aminobisphosphonates through their stimulation of gdT cells and the induction of an anti–MM activity in patient samples. Their study is a seminal finding and possibly reflects an alternative mechanism by which these drugs might play an immunomodulatory role in MM. Bisphosphonates contain 2 phosphonate groups attached to a single carbon atom, forming a ‘‘P-C-P’’ structure,2 and represent stable analogues of naturally occurring pyrophosphate-containing compounds. Bisphosphonates adsorb to bone mineral and inhibit bone resorption. On the basis of the presence of a hydroxyl group, these molecules display a high binding affinity for hydroxyapatite crystals in mineralized bone matrix, resulting in interference with osteoclastic activity and an inhibition of bone resorption. In addition to inhibition of osteoclasts, the ability of bisphosphonates to reduce the activation frequency and birth rates of new bone remodeling units, and possibly to enhance osteon mineralization, may also contribute to the reduction in pathologic fractures in patients with osteopenia. Recent studies show that bisphosphonates can be classified into at least 2 groups with different modes of action. Bisphosphonates that closely resemble pyrophosphates (such as clodronate and etidronate) can be metabolically incorporated into nonhydrolyzable analogues of adenosine triphosphate (ATP) that may inhibit ATP-dependent intracellular enzymes. The more potent nitrogen-containing bisphosphonates (such as pamidronate, alendronate, risedronate, and ibandronate) are not metabolized in this way but can inhibit enzymes of the mevalonate pathway, thereby preventing the biosynthesis of isoprenoid compounds that are essential for the posttranslational modification of small guanidine triphosphateses (GTPases). The inhibition of protein prenylation and the disruption of the function of these key regulatory proteins explain the loss of osteoclast activity and induction of apoptosis. It is of interest to note that Mundy et al3 have shown stimulation of new bone formation by statins, a group of commonly used cholesterol-lowering drugs (hydroxymethylcoenzyme A reductase inhibitors) acting further upstream in the mevalonic acid pathway, which is also a target of bisphosphonates. MM is a clonal B-cell neoplasm that affects terminally differentiated B cells, ie, plasma cells.4 In the year 2000, MM will be diagnosed in approximately 13 700 people in the United States and will account for 20% of deaths from hematologic malignancies.5 Despite the use of aggressive approaches including myeloablative therapy, this disease remains fatal. These are, however, exciting times in myeloma research. Novel therapeutic interventions such as posttransplant immunotherapy approaches6 and the use of pharmacologic interventions including drugs such as thalidomide7 offer great promise. Kunzmann et al1 report an interesting effect of bisphosphonates on T cells resulting in indirect effects on MM cells. To date, the role of bisphosphonates has been as supportive therapy for MM bone disease. Although a weak bisphosphonate, etidronate, was not found to be effective in MM bone disease,8 clodronate, which is 10 times more potent, demonstrated a significant decrease in the development of osteolytic lesions and other skeletally related complications in 2 placebo controlled randomized trials.9,10 Pamidronate, a second-generation bisphosphonate, is 100-fold more potent than etidronate and can be given intravenously. In a prospective randomized trial,11 patients with stage III MM and at least 1 lytic lesion were treated with either placebo or pamidronate (90 mg) as a 4-hour intravenous infusion given every 4 weeks for 9 cycles as a supplement to antimyeloma therapy. Among 392 patients enrolled, the efficacy of treatment could be evaluated in 196 patients who received pamidronate and 181 patients who received placebo. The proportion of patients who had any skeletal events was significantly lower in the pamidronate group (24%) than in the placebo group (41%, P , .001). Patients who received pamidronate also had significant decreases in bone pain and maintained both performance status and quality of life. Subsequently, this study was extended to 21 cycles of pamidronate therapy.12 After 21 cycles, the proportion of patients who developed any skeletal event remained lower in the pamidronate group (P 5 .015). The mean number of skeletal events per year also remained lower in the pamidronate group (1.3) than in placebotreated patients (2.2; P 5 .008). Although overall survival did not differ between the pamidronate-treated group and placebo patients, those patients receiving a second or subsequent course of chemotherapy who were randomized to also receive pamidronate lived longer than patients on salvage therapy who did not receive pamidronate (14 vs 21 months, P 5 .041). Third-generation bisphosphonates include zoledronate and ibandronate. Zoledronate is 100 to 850 times more potent than pamidronate, and studies are underway comparing pamidronate with zoledronate. The antiresorptive effect of bisphosphonates and their molecular effects on osteoclasts and osteoblasts are now being defined. Even more intriguing, however, are the insights into their novel mechanisms of actions, such as stimulating T-cell proliferation and