Assessment of rituximab-abbs, a biosimilar, and rituximab outcomes in patients with CLL or NHL: A real-world UK study

被引:7
|
作者
McBride, Ali [1 ]
Daniel, Shoshana [2 ]
Driessen, Maurice T. [3 ]
Szende, Agota [4 ]
Choudhry, Azhar [5 ]
Tian, Marc [5 ]
Ariely, Rinat [6 ]
Thompson, Stephen [6 ]
机构
[1] Univ Arizona, Dept Pharm, Hematol Oncol, Canc Ctr, 3838 N Campbell Ave, Tucson, AZ 85749 USA
[2] Covance, 9801 Washingtonian Blvd, Gaithersburg, MD 20878 USA
[3] Teva Pharmaceut Inc, Piet Heinkade 107, NL-1019 BRA Amsterdam, Netherlands
[4] Covance, Springfield House,Hyde St,Woodhouse, Leeds LS2 9LH, W Yorkshire, England
[5] Teva Pharmaceut Ind Inc, 145 Brandywine Pkwy, W Chester, PA 19380 USA
[6] Teva Pharmaceut Inc, 400 Interpace Pkwy 3, Parsippany, NJ 07054 USA
关键词
Acquisition costs; Adverse events; Clinical practice; Efficacy; Healthcare resource utilization; FOLLICULAR LYMPHOMA; DOUBLE-BLIND; CT-P10; EFFICACY; CANCER; SAFETY; PHARMACOKINETICS; PHASE-3; BURDEN;
D O I
10.1016/j.leukres.2021.106671
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Rituximab (chimeric anti-CD20 monoclonal antibody) treatment is approved for chronic lymphocytic leukemia (CLL) and non-Hodgkin lymphoma (NHL). Rituximab-abbs (first biosimilar approved in 2017) is expected to significantly reduce healthcare economic burden due to lower acquisition costs. This non interventional, non-comparative study assessed real-world effectiveness and tolerability of rituximab-abbs and rituximab in treatment-naive patients with CLL or NHL. Materials and methods: Via an online physician survey, 46 UK-registered hematologists and oncologists retrospectively reported on randomly selected patients aged >= 18 years with CLL or NHL with rituximab-abbs or rituximab as first-line immunotherapy. Overall, 201 patient charts were examined across 4 cohorts: rituximababbs in CLL, rituximab-abbs in NHL, rituximab in CLL, rituximab in NHL. Results: Demographic profiles across cohorts were similar. Most patients (94 %-100 %) received combination therapy (rituximab-abbs or rituximab mainly with chemotherapy). For both treatments, overall response rate (94 %-98 %) and 1-year overall survival (98 %-100 %) were very high for patients with CLL or NHL. Most common serious adverse events were neutropenia, fatigue, anemia and infusion reactions. The majority of patients (54 %- 66 %) did not experience a grade >= 3 adverse event. Healthcare resource utilization was similarly high across cohorts, driven by diagnostic testing, oncologist office visits, and day-case hospital admissions; many patients required supportive medical therapies. Mean annual savings of similar to 1000 pound/patient driven by acquisition costs occurred with rituximab-abbs versus rituximab, administration costs were similar. Conclusion: Rituximab-abbs and rituximab demonstrated similar effectiveness and tolerability in treating CLL and NHL in routine UK clinical practice and demonstrate the utility of the biosimilar as a cost-saving alternative treatment.
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页数:8
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