医学
来那度胺
Carfilzomib公司
达拉图穆马
梅尔法兰
多发性骨髓瘤
耐受性
内科学
硼替佐米
肿瘤科
地塞米松
蛋白酶体抑制剂
不利影响
外科
作者
Ola Landgren,Malin Hultcrantz,Benjamin Diamond,Alexander M. Lesokhin,Sham Mailankody,Hani Hassoun,Carlyn Tan,Urvi Shah,Sydney X. Lu,Meghan Salcedo,Kelly Werner,Jenna Rispoli,Julia Caple,Allison Sams,Dennis Verducci,Katie Jones,Isabel Concepcion,Ciardello Amanda,Aisara Chansakul,Julia Schlossman,Elizabet Tavitian,Tala Shekarkhand,Angela Harrison,C Piacentini,Even H Rustad,Venkata D. Yellapantula,Kylee Maclaughlan,Francesco Maura,Heather Landau,Michael Scordo,David J. Chung,Gunjan L. Shah,Oscar Lahoud,Katie Thoren,Kazunori Murata,Lakshmi V. Ramanathan,Maria E. Arcila,Caleb Ho,Mikhail Roshal,Ahmet Doğan,Andriy Derkach,Sergio Giralt,Neha Korde
出处
期刊:JAMA Oncology
[American Medical Association]
日期:2021-04-17
卷期号:7 (6): 862-862
被引量:83
标识
DOI:10.1001/jamaoncol.2021.0611
摘要
Recently, the benefit of adding daratumumab to the proteasome inhibitor-based, 3-drug combination of bortezomib, lenalidomide, and dexamethasone for patients with newly diagnosed multiple myeloma who underwent high-dose melphalan chemotherapy and autologous hemopoietic cell transplant was assessed. Here, we examine the addition of daratumumab to the second-generation proteasome inhibitor-based, 3-drug combination of carfilzomib, lenalidomide, and dexamethasone.To assess the safety and effectiveness of carfilzomib-lenalidomide-dexamethasone-daratumumab combination therapy for patients with newly diagnosed multiple myeloma, in the absence of high-dose melphalan chemotherapy and autologous hemopoietic cell transplant.Clinical and correlative pilot study at the Memorial Sloan Kettering Cancer Center in New York, New York. Patients with newly diagnosed multiple myeloma were enrolled between October 1, 2018, and November 15, 2019. The median follow-up from start of treatment was 20.3 months (95% CI, 19.2-21.9 months).Eight 28-day cycles with intravenous carfilzomib, 20/56 mg/m2 (days 1, 8, and 15); oral lenalidomide, 25 mg, (days 1-21); dexamethasone, 40 mg weekly, orally or intravenously (cycles 1-4), and 20 mg after cycle 4; and intravenous daratumumab, 16 mg/kg (days 1, 8, 15, and 22 [cycles 1-2]; days 1 and 15 [cycles 3-6]; and day 1 [cycles 7 and 8]).The primary end point was the minimal residual disease (MRD) rate, in the absence of high-dose melphalan chemotherapy and autologous hemopoietic cell transplant. Secondary end points included determining safety and tolerability, evaluating rates of clinical response per the International Myeloma Working Group, and estimating progression-free survival (PFS) and overall survival (OS) rates.Forty-one evaluable patients were enrolled (median age, 59 years; range, 30-70 years); 25 (61%) were female, and 20 (49%) had high-risk multiple myeloma. The primary end point (MRD negativity in the bone marrow; 10-5 sensitivity) was achieved in 29 of 41 patients (71%; 95% CI, 54%-83%), and therefore the trial was deemed successful. Median time to MRD negativity was 6 cycles (range, 1-8 cycles). Secondary end points of the overall response rate and the very good partial response or complete response rate were 100% (41 of 41 patients) and 95% (39 of 41 patients), respectively. At 11 months of the median follow-up, the 1-year PFS rate and the OS rate were 98% (95% CI, 93%-100%) and 100%, respectively. Most common (≥2 patients) grade 3 or 4 adverse events were neutropenia (12 patients [27%]), rash (4 patients [9%]), lung infection (3 patients [7%]), and increased alanine aminotransferase level (2 patients [4%]). There were no deaths.In this nonrandomized clinical trial, carfilzomib-lenalidomide-dexamethasone-daratumumab combination therapy was associated with high rates of MRD negativity in patients with newly diagnosed multiple myeloma and high rates of PFS.