Dose escalation study with rhenium-188 hydroxyethylidene diphosphonate in prostate cancer patients with osseous metastases

Citation
H. Palmedo et al., Dose escalation study with rhenium-188 hydroxyethylidene diphosphonate in prostate cancer patients with osseous metastases, EUR J NUCL, 27(2), 2000, pp. 123-130
Citations number
20
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
Journal title
EUROPEAN JOURNAL OF NUCLEAR MEDICINE
ISSN journal
03406997 → ACNP
Volume
27
Issue
2
Year of publication
2000
Pages
123 - 130
Database
ISI
SICI code
0340-6997(200002)27:2<123:DESWRH>2.0.ZU;2-Y
Abstract
The aim of this study was to determine the maximum tolerated dose of rheniu m-188 hydroxyethylidene diphosphonate (HEDP) in prostate cancer patients wi th osseous metastases who are suffering from bone pain, Twenty-two patients received a single injection of escalating doses of carrier-added Re-188-HE DP [1.3 GBq (35 mCi), 2.6 GBq (70 mCi), 3.3 GBq (90 mCi) and 4.4 GBq (120 m Ci)]. Blood counts and biochemical parameters were measured weekly over a p eriod of 8 weeks. Haematological toxicity (WHO grading) of grade 3 or 4 was considered unacceptable. Clinical follow-up studies including methods of p ain documentation (medication, pain diary) were performed for 6 months afte r treatment, In the 1.3-GBq group. no haematological toxicity was observed. First haematotoxic results were noted in those patients with a dose of 2.6 GBq Re-188-HEDP. In the 3.3-GBq group, one patient showed a reversible thr ombopenia of grade 1, one a reversible thrombopenia of grade 2 and three a reversible leukopenia of grade 1. In the 4.4-GBq group, thrombopenia of gra des 3 and 4 was observed in one and two patients (baseline thrombocyte coun t <200 x 10(9)/l), respectively, and leukopenia of grade 3 was documented i n one patient. The overall nadir of thrombopenia was at week 4. The individ ual, maximum percentage decrease in thrombocytes in the 1.3-, 2.6-, 3.3- an d 4.4-GBq groups was 17%, 40%, 60% and 86%, respectively. In two patients, a transient increase in serum creatinine was observed (max, 1.6 mg/dl). Pai n palliation was reported by 64% of patients, with a mean duration of 7.5 w eeks. The response rate seemed to increase with higher doses, reaching 75% in the 4.4-GBq group, It is concluded that in prostate cancer patients, the maximum tolerated dose of Re-188-HEDP is 3.3 GBq if the baseline thrombocy te count is below 200x10(9)/l, In patients with thrombocyte counts signific antly above 200x10(9)/1, a dose of 4.4 GBq might be tolerable, Thrombo- and leukopenia are the most important side-effects, Pain palliation can be ach ieved in 60%-75% of patients receiving a dose of 2.6 GBq or more of Re-188- HEDP. Studies in a larger patient population are warranted to evaluate furt her the palliative effect of Re-188-HEDP.