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成功应用按需普乐沙福进行自体外周血造血干细胞移植治疗复发/难治性生殖细胞肿瘤。

Successful "on-demand" plerixafor for autologous peripheral blood stem-cells transplantation for relapsed/refractory germ cell tumors.

机构信息

Dipartimento di Diagnostica per Immagini, Radioterapia Oncologica ed Ematologia, Fondazione Policlinico A. Gemelli IRCCS, Rome, Italy.

Medical Oncology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

出版信息

J Clin Apher. 2022 Feb;37(1):65-69. doi: 10.1002/jca.21952. Epub 2021 Nov 25.

Abstract

BACKGROUND

Germ cell tumors represent, among solid cancers, a potentially curable disease even if up to 20% to 30% of patients (pts) relapse after first-line treatment especially considering intermediate and poor prognosis groups. In this scenario, patients are candidates for high-dose chemotherapy and autologous stem-cells transplantation as second-line treatment even though stem-cells mobilization potential can be affected by several cycles and regimens of chemotherapy. To date, plerixafor is authorized in poor mobilizer adult pts diagnosed with lymphoma or multiple myeloma and in pediatric solid tumors or lymphoma. Therefore, the use of plerixafor in adult pts with relapsing/refractory GCT is still off label.

MATERIALS AND METHODS

In our study, we describe mobilization and collection of peripheral blood stem cells for 10 pts with germ cell tumors. Six patients underwent plerixafor administration since classified as poor mobilizers based on WBC count (>5.000/μL) and CD34+ cell count (<15/μL) the day before apheresis procedure.

RESULTS

On the first day of apheresis, plerixafor administration in poor mobilizers made possible a remarkable boost of CD34+ cells in such a way to overlap that of good mobilizers' (32/μL vs 35/μL, respectively, P > .05).

CONCLUSION

Therefore, in our experience, plerixafor made a good fraction of poor mobilizer patients eligible for mobilization and collection and able to undergo the predicted autologous stem-cells transplantation; thus, the lack of access to the use of plerixafor in this setting of patients risks jeopardizing an effective treatment, especially in case of poor prognosis.

摘要

背景

在实体瘤中,生殖细胞肿瘤是一种潜在可治愈的疾病,即使在一线治疗后仍有 20%至 30%的患者(pts)复发,尤其是考虑到中危和高危预后组。在这种情况下,即使化疗的多个周期和方案可能会影响干细胞动员潜能,患者仍可作为二线治疗选择接受高剂量化疗和自体干细胞移植。迄今为止,plerixafor 已被批准用于治疗诊断为淋巴瘤或多发性骨髓瘤的低动员成人 pts,以及儿科实体瘤或淋巴瘤。因此,plerixafor 在复发/难治性生殖细胞肿瘤成人患者中的使用仍然是超适应证的。

材料和方法

在我们的研究中,我们描述了 10 例生殖细胞肿瘤患者外周血干细胞的动员和采集情况。6 例患者因白细胞计数(>5000/μL)和 CD34+细胞计数(<15/μL)在前一天的外周血干细胞采集前被归类为低动员者而接受了 plerixafor 治疗。

结果

在第一次采集日,低动员者使用 plerixafor 治疗后 CD34+细胞数量显著增加,与高动员者的 CD34+细胞数量相当(分别为 32/μL 和 35/μL,P>.05)。

结论

因此,根据我们的经验,plerixafor 使相当一部分低动员者有资格进行动员和采集,并能够进行预期的自体干细胞移植;因此,在这种情况下,缺乏对 plerixafor 的使用会危及有效的治疗,尤其是在预后较差的情况下。

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