Abstract

BackgroundThe efficacy and safety of rituximab-based chemotherapy (R-chemo), the standard regimen for patients with diffuse large B-cell lymphoma (DLBCL), which is more common in Asia than in Western countries, are well confirmed in randomized controlled trials (RCTs). However, the safety and effectiveness of R-chemo in patients who are largely excluded from RCTs have not been well characterized. This real-world study investigated the safety and effectiveness of R-chemo as first-line treatment in Chinese patients with DLBCL.MethodsTreatment-naive DLBCL patients who were CD20 positive and eligible to receive R-chemo were enrolled with no specific exclusion criteria. Data collected at baseline included age, gender, disease stage, international prognostic index (IPI), B symptoms, extranodal involvement, performance status, and medical history. In the present study, data on safety, treatment effectiveness, and HBV infection management were collected 120 days after the last R-chemo administration.ResultsOverall, R-chemo was well tolerated. The safety profile of R-chemo in patients with a history of heart or liver disease was well described without any additional unexpected safety concerns. The overall response rate (ORR) in the Chinese patients from this study was 94.2 % (complete response [CR], 55.0 %; CR unconfirmed [CRu] 18.2 %; and partial response [PR], 20.9 %). Compared to patients with no history of disease, the CR and PR rates of patients with a history of heart or liver disease were lower and higher, respectively; this tendency could be in part explained by treatment interruptions in patients with heart or liver diseases. HBsAg positivity and a maximum tumor diameter of ≥7.5 cm negatively correlated with CR + CRu, whereas age and HBsAg positivity negatively correlated with CR.ConclusionsThis study further validated the safety and effectiveness of R-chemo in Chinese patients with DLBCL. Patients with a history of heart or liver disease may further benefit from R-chemo if preventive measures are taken to reduce hepatic and cardiovascular toxicity. In addition to IPI and tumor diameter, HBsAg positivity could also be a poor prognostic factor for CR in Chinese patients with DLBCL.Trial registrationClinicalTrials.gov #NCT01340443, April 20, 2011.Electronic supplementary materialThe online version of this article (doi:10.1186/s12885-016-2523-7) contains supplementary material, which is available to authorized users.

Highlights

  • The efficacy and safety of rituximab-based chemotherapy (R-chemo), the standard regimen for patients with diffuse large B-cell lymphoma (DLBCL), which is more common in Asia than in Western countries, are well confirmed in randomized controlled trials (RCTs)

  • The FDA recently issued a warning that patients receiving immune-suppressing rituximab or ofatumumab are at an increased risk of hepatitis B virus (HBV) reactivation [13]

  • Because HBV infection is highly endemic in China, 12–27 % of all Chinese patients with non-Hodgkin lymphoma (NHL) are positive for hepatitis B surface antigen (HBsAg), which increases the risk of HBV reactivation [14,15,16,17]

Read more

Summary

Introduction

The efficacy and safety of rituximab-based chemotherapy (R-chemo), the standard regimen for patients with diffuse large B-cell lymphoma (DLBCL), which is more common in Asia than in Western countries, are well confirmed in randomized controlled trials (RCTs). The safety and effectiveness of R-chemo in patients who are largely excluded from RCTs have not been well characterized. The FDA recently issued a warning that patients receiving immune-suppressing rituximab or ofatumumab are at an increased risk of hepatitis B virus (HBV) reactivation [13]. Because HBV infection is highly endemic in China, 12–27 % of all Chinese patients with NHL are positive for hepatitis B surface antigen (HBsAg), which increases the risk of HBV reactivation [14,15,16,17]. A recent study in China reported HBV reactivation in approximately 17.1 % of HBsAg-positive (pos) patients receiving R-chemo [20]

Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call