首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >Bone marrow recovery following use of systemic (153)Sm-lexidronam and (89)Sr-chloride for bone pain palliation after myelosuppressive therapy.
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Bone marrow recovery following use of systemic (153)Sm-lexidronam and (89)Sr-chloride for bone pain palliation after myelosuppressive therapy.

机译:在骨髓抑制治疗后使用全身性(153)Sm-lexidronam和(89)Sr-氯化物缓解骨痛后,骨髓恢复。

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PURPOSE: Using plasma flt3 ((FMS (Friend murine strain))-like tyrosine kinase 3)-ligand cytokine (FL) as a biomarker, the purpose of this study was to determine whether patients receiving palliative radionuclide treatment following chemotherapy experienced enhanced myelosuppression. MATERIALS AND METHODS: A total of 48 patients with solid tumors who failed multi-agent chemotherapy were investigated; they previously received 1-3 cycles of combination chemotherapy over 4-10 months. Patients were divided into four cohorts including 10 patients with early stage solid tumors prior to chemotherapy induction (naive group), 10 patients with (non-metastatic) malignancy actively undergoing chemotherapy without radionuclide follow-up (chemotherapy-alone group), 13 patients who underwent standard (1.0 mCi/kg) dose (153)Sm ((153)samarium)-lexidronam therapy following chemotherapy ((153)Sm group), and 15 patients who underwent standard (4 mCi) dose (89)Sr ((89)strontium)-chloride therapy following chemotherapy ((89)Sr group). Plasma FL was measured using a quantitative sandwich enzyme immunoassay and CBC (complete blood count), measuring WBC (white blood cell) and PLT (platelet), was performed. RESULTS: Plasma FL concentration demonstrated a gradual decrease after chemotherapy. In patients who received (153)Sm within two weeks of completing chemotherapy, there is a distinguishable spike in FL concentration at approximately three weeks after dose administration, which precedes a decrease in WBC and PLT counts. On the other hand, a spike in FL levels in patients who received (89)Sr therapy is noted at approximately 10 weeks (p < 0.034). CONCLUSIONS: Increases in FL concentration associated with (153)Sm-lexidronam therapy following combination chemotherapy occurred earlier and returned to control levels more rapidly than did those in patients similarly treated with (89)Sr. These differences might be associated with the shorter decay half-life and lower particle emission energies of (153)Sm.
机译:目的:使用血浆flt3((FMS(Friend鼠类))酪氨酸激酶3)-配体细胞因子(FL)作为生物标志物,本研究的目的是确定化疗后接受姑息性放射性核素治疗的患者骨髓抑制是否增强。材料与方法:共调查了48例多药化疗失败的实体瘤患者。他们先前在4-10个月内接受了1-3个周期的联合化疗。将患者分为四组,其中包括10例在诱导化疗前出现早期实体瘤的患者(未治疗组),10例未进行放射性核素随访而积极接受化疗的(非转移性)恶性肿瘤(仅化疗组),13例化疗后((153)Sm组)接受标准剂量(1.0 mCi / kg)(153)Sm((153)))-来昔多南治疗,15例患者接受了标准剂量(4 mCi)(89)Sr((89 (89)锶组)。)使用定量夹心酶免疫测定法测量血浆FL,并进行CBC(全血细胞计数),测量WBC(白细胞)和PLT(血小板)。结果:化疗后血浆FL浓度逐渐降低。在完成化疗的两周内接受(153)Sm的患者,在给药后约三周,FL浓度明显升高,这是在WBC和PLT计数降低之前。另一方面,在大约10周时,接受(89)Sr治疗的患者的FL水平达到峰值(p <0.034)。结论:与(89)Sr相似的患者相比,联合化疗后与(153)Sm-lexidronam疗法相关的FL浓度升高更早发生,并更快地回到控制水平。这些差异可能与较短的衰减半衰期和较低的(153)Sm粒子发射能量有关。

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