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Efficacy of Subcutaneous Bortezomib in the Management of Patients with Multiple Myeloma or Relapsed Mantle Cell Lymphoma

机译:皮下硼替佐米治疗多发性骨髓瘤或复发性套细胞淋巴瘤的疗效

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The identification of the ubiquitin–proteasome system as a new therapeutic target has been one of the most recent successes in cancer treatment. The development and clinical approval of the first-in-class proteasome inhibitor, bortezomib has revolutionized the treatment of multiple myeloma (MM) and mantle cell lymphoma (MCL). In MM, bortezomib is now integrated in induction, conditioning, consolidation, maintenance, and salvage treatment protocols. Bortezomib-based regimens provide high remission rates and confer significant survival advantage compared to conventional chemotherapy in both the bone marrow transplant and non-transplant setting. In MCL, overall response rates in patients who have received at least one prior therapy range from 30 to 45%, even in chemotherapy resistant patients. Clinical trials to further improve the sequencing of bortezomib-containing combination therapies are ongoing. Until recently, intravenous injection was the standard route of bortezomib administration. However, severe adverse side effects, peripheral neuropathy in particular, were observed in up to 16% of MM patients and up to 54% of MCL patients treated with intravenous bortezomib, with grade 3 and 4 in 11 and 12% of patients, respectively. Moreover, complete remission rates, if at all, are low and duration of response is short both in MM and MCL. These limitations may be overcome by changing the method of bortezomib administration as well as by rationally combining bortezomib with other therapeutic agents. Indeed, recent data demonstrate that subcutaneous bortezomib administration is non-inferior to intravenous administration, with an improved systemic safety profile, good local tolerance, and a more convenient route of administration. Based on these data, subcutaneous bortezomib injection was approved as a supplemental new drug application for all approved indications in MM and MCL after at least one prior therapy. More than 30 clinical trials in MM and MCL are currently ongoing to evaluate the efficacy and safety profile of subcutaneous bortezomib also in induction, maintenance, and salvage therapy.
机译:将泛素-蛋白酶体系统鉴定为新的治疗靶点已成为癌症治疗领域的最新成功之一。一流的蛋白酶体抑制剂硼替佐米的开发和临床批准,彻底改变了多发性骨髓瘤(MM)和套细胞淋巴瘤(MCL)的治疗方法。在MM中,硼替佐米现已集成到诱导,调节,巩固,维护和挽救治疗方案中。与常规化疗相比,基于硼替佐米的方案在骨髓移植和非移植治疗中均具有较高的缓解率,并具有明显的生存优势。在MCL中,即使接受过化疗的患者,接受过至少一种先前治疗的患者的总体缓解率在30%至45%之间。正在进行进一步改善含硼替佐米的联合疗法测序的临床试验。直到最近,静脉注射一直是硼替佐米给药的标准途径。但是,在接受静脉注射硼替佐米治疗的MM患者中,多达16%和MCL患者中观察到严重的不良副作用,尤其是周围神经病变,分别在11%和12%的患者中达到3级和4级。此外,MM和MCL的完全缓解率(如果有的话)都很低,响应时间也很短。这些局限性可以通过改变硼替佐米的给药方法以及将硼替佐米与其他治疗药物合理组合来克服。实际上,最近的数据表明皮下注射硼替佐米不逊于静脉内给药,具有改善的全身安全性,良好的局部耐受性和更方便的给药途径。基于这些数据,在至少一种先前的治疗后,皮下注射硼替佐米注射液被批准作为MM和MCL中所有已批准适应症的补充新药应用。目前正在进行MM和MCL的30多项临床试验,以评估皮下硼替佐米在诱导,维持和挽救治疗中的功效和安全性。

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