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Following intravenous injection, soluble strontium compounds behave like their calcium analogs, clearing rapidly from the blood and selectively localizing in bone mineral. Uptake of strontium by bone occurs preferentially in sites of active osteogenesis; thus primary bone tumors and areas of metastatic invo l vement (blastic lesions) can accumulate significantly gre a ter concentrations of strontium than surrounding normal bone.
Strontium-89 Chloride is retained in metastatic bone lesions much longer than in normal bone, where turnover is about 14 days. In patients with extensive skeletal metastases, well over half of the injected dose is retained in the bones.
Excretion pathways are two-thirds urinary and one-third fecal in patients with bone metastases. Urinary excretion is higher in people without bone lesions. Urinary excretion is greatest in the first two days following injection.
Strontium-89 is a pure beta emitter and Strontium-89 Chloride selectively irradiates sites of primary and metastatic bone involvement with minimal irradiation of soft tissues distant from the bone lesions. (The maximum range in tissue is 8 mm; maximum energy is 1.463 MeV.) Mean absorbed radiation doses are listed under the Radiation Dosimetry section.
Clinical trials have examined relief of pain in cancer patients who have received therapy for bone metastases (external radiation to indexed sites) but in whom persistent pain recurred. In a multi-center Canadian placebo-controlled trial of 126 patients, pain relief occurred in more patients treated with a single injection of Metastron (strontium-89) than in patients treated with an injection of placebo. Results are given in the following tables.
Table 2 compares the percentage and number of patients treated with Metastron (strontium-89) or placebo who had reduced pain and no increase in analgesic or radiotherapy re-treatment.
Table 2: Comparison of the effects of St rontium-89 and placebo,
as adjunct to radiotherapy, on treatment outcome over time.
At each visit, treatment success, defined as a reduction in a patient's pain score without any increase in analgesic intake and without any supplementary radiotherapy at the index site, was more frequent among patients assigned to Metastron (strontium-89) than to placebo.
Table 3 compares the number and percentage of patients t re a ted with Metastron (strontium-89) or placebo as an adjunct to radiotherapy who were pain free without analgesic at the intervals shown.
Table 3: Comparison of the effects of Strontium-89 and placebo,
as adjunct to radiotherapy, on reduction of pain score and analgesic score to
The number of patients classified at each visit as treatment successes who were pain free at the index site and required no analgesics was consistently higher in the Metastron (strontium-89) group.
New pain sites were less frequent in patients treated with Metastron (strontium-89) .
In another clinical trial, pain relief was greater in a group of patients tre a ted with Metastron (strontium-89) compared with a group treated with non-radioactive strontium-88.
Last reviewed on RxList: 1/29/2009
This monograph has been modified to include the generic and brand name in many instances.
Additional Metastron Information
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