Lewington Val J
Royal Marsden Hospital, Sutton, England, United Kingdom.
J Nucl Med. 2005 Jan;46 Suppl 1:38S-47S.
Systemic therapy using bone-seeking radiopharmaceuticals has clear advantages for the treatment of multisite metastatic pain. Evidence supporting the use of beta-particle, electron, and alpha-particle-emitting radiopharmaceuticals is reviewed here. Appropriate patient selection relies on correlating clinical symptoms with focal abnormalities on conventional bone scintigraphy. Time to symptom relief and response duration vary with the physical half-life and dose rate of the radionuclide used, offering the opportunity to tailor radiopharmaceutical choice to individual patient circumstances. Toxicity is limited to temporary myelosuppression, governed by the administered activity and underlying bone marrow reserve. Optimal responses are achieved in patients with a modest skeletal tumor burden, suggesting that targeted therapy should be considered early in the management of bone metastases. The development of reliable dosimetric models will facilitate patient-specific prescribing to deliver enhanced symptom response within acceptable toxicity limits. It is likely that targeted therapy will be most effective in the context of multimodality tumor management. Further research is required to examine the potential of radionuclides in combination with external-beam irradiation, bisphosphonates, or chemotherapy. This approach might allow targeted therapy to progress beyond symptom palliation to early intervention for survival gain.
使用亲骨性放射性药物的全身治疗在多部位转移性疼痛的治疗中具有明显优势。本文综述了支持使用发射β粒子、电子和α粒子的放射性药物的证据。合适的患者选择依赖于将临床症状与传统骨闪烁显像上的局灶性异常相关联。症状缓解时间和反应持续时间随所用放射性核素的物理半衰期和剂量率而变化,这为根据个体患者情况调整放射性药物的选择提供了机会。毒性仅限于暂时的骨髓抑制,其受给药活度和潜在骨髓储备的控制。骨骼肿瘤负荷适中的患者可实现最佳反应,这表明在骨转移的管理中应尽早考虑靶向治疗。可靠的剂量学模型的开发将有助于根据患者具体情况进行给药,以在可接受的毒性范围内实现更好的症状反应。在多模式肿瘤管理的背景下,靶向治疗可能最有效。需要进一步研究来考察放射性核素与外照射、双膦酸盐或化疗联合使用的潜力。这种方法可能使靶向治疗从症状缓解发展到早期干预以提高生存率。