Tessenow Hannah, Holzvogt Madlen, Holzvogt Bruno, Andrea Marc, Heyn Simone, Schliwa Thomas, Schwarz Maik, Zehrfeld Thomas, Becker Cornelia, Pfrepper Christian, Franke Georg Nikolaus, Krahl Rainer, Jentzsch Madlen, Leiblein Sabine, Schwind Sebastian, Bill Marius, Vucinic Vladan, Lange Thoralf, Niederwieser Dietger, Pönisch Wolfram
University Hospital Leipzig, Leipzig, Germany.
Hospital Weissenfels, Weissenfels, Germany.
J Cancer Res Clin Oncol. 2017 Oct;143(10):2049-2058. doi: 10.1007/s00432-017-2439-x. Epub 2017 May 22.
Patients with light chain myeloma frequently have a light chain tubular cast nephropathy, which can lead to severe renal impairment. In the present retrospective study, bortezomib was combined with other active substances like bendamustine and prednisone (BPV), in order to assess the efficacy and toxicity of the combination therapy in patients with light chain multiple myeloma.
Between September 2008 and May 2015, 25 patients with newly diagnosed light chain multiple myeloma were treated with bendamustine 60 mg/m on days 1 and 2, bortezomib 1.3 mg/m on days 1, 4, 8 and 11, and prednisone 100 mg on days 1, 2, 4, 8 and 11 once every 21 days (BPV). Prior to treatment, 4 patients (16%) had moderate renal dysfunction and 14 patients (56%) severe renal dysfunction or renal failure/dialysis.
The median number of the BPV cycles was 2 (1-5). 24 patients (96%) responded with 4 stringent complete responses, 6 near-complete responses, 5 very good partial responses and 9 partial responses. The myeloma light chains decreased rapidly, reaching the best response after the first cycle in 9 and after the second cycle in additional 12 patients. 17 patients discontinued therapy after median 2 cycles of BPV treatment to receive autologous or allogeneic SCT. All together 12 of 18 patients with at least moderate renal failure improved their renal function. 3 of the 6 dialysis-dependent patients became dialysis-independent. With a median follow-up of 27 months, median progression-free survival and overall survival for patients at 30 months were 68 and 96%, respectively. The most common severe side effect was grade 3/4 leukocytopenia in 20% of the patients. Grade 3/4 thrombocytopenia was observed in 12% of the patients. Moderate to severe infection were seen in six patients. We conclude that BPV is effective and well tolerated in patients with newly diagnosed/untreated light chain multiple myeloma.
轻链型骨髓瘤患者常伴有轻链管型肾病,可导致严重肾功能损害。在本回顾性研究中,硼替佐米与苯达莫司汀和泼尼松等其他活性物质联合使用(BPV),以评估该联合疗法对轻链多发性骨髓瘤患者的疗效和毒性。
2008年9月至2015年5月期间,25例新诊断的轻链多发性骨髓瘤患者接受治疗,第1天和第2天给予苯达莫司汀60mg/m²,第1、4、8和11天给予硼替佐米1.3mg/m²,第1、2、4、8和11天给予泼尼松100mg,每21天一次(BPV)。治疗前,4例患者(16%)有中度肾功能不全,14例患者(56%)有严重肾功能不全或肾衰竭/透析。
BPV治疗周期的中位数为2(1 - 5)。24例患者(96%)有反应,其中4例严格完全缓解,6例接近完全缓解,5例非常好的部分缓解,9例部分缓解。骨髓瘤轻链迅速下降,9例患者在第一个周期后达到最佳反应,另外12例患者在第二个周期后达到最佳反应。17例患者在接受BPV治疗中位数2个周期后停止治疗,接受自体或异基因造血干细胞移植。18例至少有中度肾衰竭的患者中,共有12例肾功能得到改善。6例依赖透析的患者中有3例不再依赖透析。中位随访27个月,30个月时患者的无进展生存期和总生存期的中位数分别为68%和96%。最常见严重副作用是20%的患者出现3/4级白细胞减少。12%的患者观察到3/4级血小板减少。6例患者出现中度至重度感染。我们得出结论,BPV对新诊断/未治疗的轻链多发性骨髓瘤患者有效且耐受性良好。