Tu Shi-Ming, Kim Jeri, Pagliaro Lance C, Vakar-Lopez Funda, Wong Frankin C, Wen Sijin, General Rosales, Podoloff Donald A, Lin Sue-Hwa, Logothetis Christopher J
Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, 77030, USA.
J Clin Oncol. 2005 Nov 1;23(31):7904-10. doi: 10.1200/JCO.2005.01.2310.
Clinicians may have reservations about using strontium-89 for the treatment of bone metastases because of concerns that it may limit future use of chemotherapy. We assessed the rate of bone marrow failure in patients with prostate cancer who had received a dose of strontium-89.
This subgroup analysis involved 34 patients with androgen-independent prostate cancer who had been given a dose of strontium-89 and six weekly doses of doxorubicin after response to induction chemotherapy. We assessed subsequent hematotoxicity in terms of bone marrow failure and the ability to tolerate additional treatments during a median of 25 months (range, 7 to 76 months) after the strontium-89 was administered.
No patients developed bone marrow failure within 6 months of receiving strontium-89. Five (15%) of 34 patients developed bone marrow failure at a median 23 months (range, 6 to 53 months) after the strontium-89 treatment. Bone marrow biopsy performed in two of these five patients showed complete replacement of the marrow by tumor. Thirty-one patients (91%) received subsequent cytotoxic treatments at a median 11 months (range, 1 to 33 months) after the strontium-89 treatment.
This analysis demonstrated that a single dose of strontium-89 combined with chemotherapy did not affect the delivery of subsequent courses of chemotherapy in a select group of patients. However, a majority of these therapies were given off protocol and were administered at a dose schedule that might be considered inappropriate or inadequate. The clinical role and safety profile of radiopharmaceuticals combined with chemotherapy in prostate cancer therapy deserve further exploration.
临床医生可能对使用锶 - 89治疗骨转移有所保留,因为担心它可能会限制未来化疗的使用。我们评估了接受过一剂锶 - 89的前列腺癌患者的骨髓衰竭发生率。
这项亚组分析纳入了34例雄激素非依赖性前列腺癌患者,这些患者在诱导化疗有反应后接受了一剂锶 - 89和六周剂量的阿霉素。我们在给予锶 - 89后的中位25个月(范围7至76个月)内,根据骨髓衰竭情况以及耐受额外治疗的能力评估了后续的血液毒性。
在接受锶 - 89后的6个月内,没有患者发生骨髓衰竭。34例患者中有5例(15%)在锶 - 89治疗后的中位23个月(范围6至53个月)发生骨髓衰竭。在这5例患者中的2例进行的骨髓活检显示骨髓被肿瘤完全替代。31例患者(91%)在锶 - 89治疗后的中位11个月(范围1至33个月)接受了后续的细胞毒性治疗。
该分析表明,在一组特定患者中,单剂量锶 - 89联合化疗并不影响后续化疗疗程的进行。然而,这些治疗中的大多数是偏离方案进行的,并且是以可能被认为不合适或不足的剂量方案给药。放射性药物联合化疗在前列腺癌治疗中的临床作用和安全性值得进一步探索。