Piasentier Alberto, Fanti Alessandro, Birtolo Maria Francesca, Vena Walter, Colle Roberto, Gentile Lucrezia Maria Silvana, Jaafar Simona, Bossi Antonio Carlo, Lania Andrea G, Mazziotti Gherardo
Department of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Via Rita Levi Montalcini 4, Milan, Italy.
Endocrinology, Diabetology and Medical Andrology Unit, IRCCS Humanitas Research Hospital, Rozzano, MI, Italy.
J Endocrinol Invest. 2025 May;48(5):1249-1256. doi: 10.1007/s40618-025-02542-3. Epub 2025 Jan 31.
The real-world effectiveness of switching from denosumab to romosozumab remains controversial. Sequential therapy with romosozumab was shown to be associated with inadequate suppression of bone resorption and there was anecdotal evidence of major osteoporotic fractures (MOFs) after transitioning from denosumab to romosozumab. This study evaluated the effects on bone resorption of early romosozumab administration 3 months after denosumab withdrawal in fractured women with post-menopausal osteoporosis.
This prospective, single-center cohort study included 39 post-menopausal women with osteoporosis experiencing either MOFs or decrease in bone mineral density during long-term treatment with anti-resorptive drugs. Eighteen received romosozumab either 6 months (Group A) or 3 months (Group B) after their last denosumab dose, while 21 women switched from bisphosphonates to romosozumab and were enrolled as controls (Group C). Serum C-terminal telopeptide of type I collagen (CTX) levels were measured at baseline, 3 and 6 months.
All women of group A and 4 out of 8 women of group B showed a clinically significant increase of CTX values (i.e., change above the least significant change) (p = 0.023), which occurred earlier in group A as compared to group B. Moreover, 9/10 women of group A and 2/8 women of group B achieved values above the mean of reference range for pre-menopausal women (p = 0.013). In group C, serum CTX values did not change significantly during the follow-up. Two women in Group A experienced MOFs during the follow-up.
Early romosozumab administration after denosumab withdrawal may control bone turnover rebound and possibly prevent incidence of fractures in post-menopausal osteoporosis.
从地诺单抗转换为罗莫单抗在现实世界中的有效性仍存在争议。罗莫单抗序贯治疗显示与骨吸收抑制不足有关,并且有轶事证据表明从地诺单抗转换为罗莫单抗后发生了严重骨质疏松性骨折(MOF)。本研究评估了在绝经后骨质疏松性骨折女性中,地诺单抗停药3个月后早期使用罗莫单抗对骨吸收的影响。
这项前瞻性、单中心队列研究纳入了39名绝经后骨质疏松女性,她们在长期抗吸收药物治疗期间发生了MOF或骨密度下降。18名女性在最后一剂地诺单抗后6个月(A组)或3个月(B组)接受罗莫单抗治疗,而21名从双膦酸盐转换为罗莫单抗的女性作为对照组(C组)。在基线、3个月和6个月时测量血清I型胶原C末端肽(CTX)水平。
A组所有女性和B组8名女性中的4名显示CTX值有临床显著升高(即变化超过最小显著变化)(p = 0.023),A组比B组更早出现。此外,A组10名女性中的9名和B组8名女性中的2名达到了绝经前女性参考范围平均值以上的值(p = 0.013)。在C组中,随访期间血清CTX值没有显著变化。A组有2名女性在随访期间发生了MOF。
地诺单抗停药后早期使用罗莫单抗可能控制骨转换反弹,并可能预防绝经后骨质疏松症的骨折发生率。