BACKGROUND:The treatment landscape for multiple myeloma (MM) has progressed significantly, and over the past decade, bortezomib-based induction therapy has been a standard of care. However, the practice of antibacterial prophylaxis during induction therapy has been diverse. The aim of our study is to evaluate the proportion of patients with febrile episodes and bacteremia among patients with MM, during the first 12 weeks of bortezomib-based induction therapy, without routine fluoroquinolone prophylaxis, but with routine Pneumocystis Carinii prophylaxis (mostly with trimethoprim-sulfamethoxazole), in a region with high fluoroquinolone resistance rate. Of note, these patients have direct access to health care facilities and timely supportive care. PATIENTS AND METHODS:We evaluated newly diagnosed MM patients from 2014 to 2018 receiving bortezomib-based induction therapy for the proportion of patients who had febrile episodes and bacteremia in the first 12 weeks of bortezomib-based induction therapy. We also evaluated if there were factors associated with increased febrile episodes including age, absolute neutrophil count, creatinine clearance, M-band level at diagnosis, nadir platelet count, International Staging System, and Revised International Staging System. RESULTS:Of the 108 evaluable patients, there were a total of 25 (23.1%) patients who had febrile episodes, and 1 (0.9%) patient who had bacteremia during the first 12 weeks of bortezomib-based induction therapy. All patients recovered well. No deaths were seen. Febrile episodes were associated with lower absolute neutrophil count (P = .036), renal impairment (P = .013), and ISS stage (P = .026). CONCLUSION:The proportion of patients with significant bacterial infection during the first 12 weeks of bortezomib-based induction therapy without routine fluoroquinolone prophylaxis, but with routine Pneumocystis Carinii prophylaxis (mostly with trimethoprim-sulfamethoxazole), is low in a population with adequate access to health care facilities and timely supportive care.

译文

摘要背景:多发性骨髓瘤(MM)的治疗领域已取得重大进展,并且在过去的十年中,基于硼替佐米的诱导治疗已成为治疗的标准。但是,在诱导疗法中进行抗菌预防的方法多种多样。我们研究的目的是评估在基于硼替佐米的诱导治疗的前12周,没有常规氟喹诺酮预防措施,但有常规肺囊虫Carinii预防措施(主要是甲氧苄氨嘧啶,氟喹诺酮耐药率较高的区域。值得注意的是,这些患者可以直接使用卫生保健设施并及时获得支持治疗。
患者和方法:我们评估了2014年至2018年接受基于硼替佐米为基础的诱导治疗的新诊断MM患者在基于硼替佐米为基础的诱导治疗的前12周中出现高热发作和菌血症的患者的比例。我们还评估了是否有与高热发作相关的因素,包括年龄,绝对中性粒细胞计数,肌酐清除率,诊断时的M带水平,最低点血小板计数,国际分期系统和修订的国际分期系统。
结果:在108名可评估的患者中,在基于硼替佐米的诱导治疗的前12周中,共有25例(23.1%)出现高热发作,1例(0.9%)出现菌血症。所有患者康复良好。没有看到死亡。高热发作与较低的绝对中性粒细胞计数(P = .036),肾功能不全(P = .013)和ISS分期(P = .026)有关。
结论:在以硼替佐米为基础的诱导治疗的前12周,未常规预防氟喹诺酮但常规预防卡氏肺孢子虫(主要采用甲氧苄啶-磺胺甲基异恶唑)的患者中,发生严重细菌感染的患者比例较低。护理设施和及时的支持性护理。

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