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对于五例华氏巨球蛋白血症患者,奥妥珠单抗、苯达莫司汀和地塞米松的联合治疗比上一线治疗取得了更深的缓解。

The treatment combination of obinutuzumab, bendamustine and dexamethasone achieved a deeper response than the previous line of treatment in five patients with Waldenström's macroglobulinemia.

作者信息

Adam Z, Pour L, Krejčí M, Sandecká V, Štork M, Boichuk I, Král Z

出版信息

Klin Onkol. 2024;37(6):427-432. doi: 10.48095/ccko2024427.

Abstract

BACKGROUND

Rituximab is already a standard part of the treatment of patients with Waldenström's macroglobulinemia. However, a small proportion of patients develop intolerance to rituximab during administration or the treatment is not very effective. In these patients, we are faced with the question of whether another anti-CD20 monoclonal antibody can be used and what result will be achieved.

PATIENT POPULATION AND METHODS

Between 2020 and 2022, we administered the new anti-CD20 monoclonal antibody obinutuzumab in combination with bendamustine and dexamethasone in five patients with Waldenström's macroglobulinemia (WM). All patients completed eight cycles of the indicated treatment. Two of them received second-line treatment, another two received third-line treatment, and one patient received this treatment as part of fourth-line treatment. We did not observe significant toxicity (grade III and IV) in any patient.

RESULTS

All five patients achieved a deeper treatment response (once complete response, 4-times very good partial response) than in previous lines of treatment. At a median follow-up after treatment of 29 months (range 28-48), the disease relapsed in one patient only, the others are in remission.

CONCLUSION

Obinutuzumab in combination with bendamustine is a very effective treatment alternative for WM. In the described five patients, obinutuzumab with bendamustine and dexamethasone achieved a deeper therapeutic response than the previous treatment lines. Obinutuzumab represents a drug that will be of great benefit to selected patients with WM.

摘要

背景

利妥昔单抗已经是华氏巨球蛋白血症患者治疗的标准组成部分。然而,一小部分患者在给药过程中出现对利妥昔单抗不耐受,或者治疗效果不佳。对于这些患者,我们面临着是否可以使用另一种抗CD20单克隆抗体以及会取得什么结果的问题。

患者群体与方法

在2020年至2022年期间,我们对5例华氏巨球蛋白血症(WM)患者使用新型抗CD20单克隆抗体奥滨尤妥珠单抗联合苯达莫司汀和地塞米松进行治疗。所有患者均完成了8个周期的指定治疗。其中2例接受二线治疗,另外2例接受三线治疗,1例患者接受此治疗作为四线治疗的一部分。我们在任何患者中均未观察到显著毒性(III级和IV级)。

结果

所有5例患者均获得了比之前治疗线更深的治疗反应(1次完全缓解,4次非常好的部分缓解)。治疗后的中位随访时间为29个月(范围28 - 48个月),仅1例患者疾病复发,其他患者均处于缓解状态。

结论

奥滨尤妥珠单抗联合苯达莫司汀是WM非常有效的治疗选择。在所描述的5例患者中,奥滨尤妥珠单抗联合苯达莫司汀和地塞米松比之前的治疗线取得了更深的治疗反应。奥滨尤妥珠单抗是一种将对选定的WM患者大有裨益的药物。

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