Cancer Res Treat.  2015 Apr;47(2):173-181. 10.4143/crt.2014.055.

Treatment Outcomes of Rituximab Plus Hyper-CVAD in Korean Patients with Sporadic Burkitt or Burkitt-like Lymphoma: Results of a Multicenter Analysis

Affiliations
  • 1Department of Internal Medicine, Gachon University Gil Medical Center, Incheon, Korea.
  • 2Department of Medicine, Samsung Medical Center, Sunkyunkwan University School of Medicine, Seoul, Korea. kstwoh@skku.edu
  • 3Department of Hematology-Oncology, Chonnam National University Hwasun Hospital, Hwasun, Korea.
  • 4Department of Hematology-Oncology, Pusan National University Hospital, Busan, Korea.
  • 5Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
  • 6Department of Internal Medicine, Kosin University Gospel Hospital, Busan, Korea.
  • 7Department of Internal Medicine, Chonbuk National University Hospital, Jeonju, Korea.
  • 8Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • 9Department of Internal Medicine, Yeungnam University Medical Center, Daegu, Korea.
  • 10Department of Internal Medicine, Dong-A University Hospital, Busan, Korea.
  • 11Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
  • 12Department of Internal Medicine, Ewha Womans University Mokdong Hospital, Seoul, Korea.
  • 13Department of Hematology-Oncology, Keimyung University Dongsan Medical Center, Keimyung University School of Medicine, Daegu, Korea.
  • 14Department of Internal Medicine, Daegu Catholic University Medical Center, Daegu, Korea.

Abstract

PURPOSE
This study was conducted to evaluate outcomes in adult patients with Burkitt lymphoma (BL) or Burkitt-like lymphoma treated with an rituximab plus hyper-CVAD (R-hyper-CVAD) regimen by focusing on tolerability and actual delivered relative dose intensity (RDI).
MATERIALS AND METHODS
Patients > or = 20 years of age and pathologically diagnosed with BL or Burkitt-like lymphoma were treated with at least one cycle of R-hyper-CVAD as the first-line treatment in this study. Eligible patients' case report forms were requested from their physicians to obtain clinical and laboratory data for this retrospective study.
RESULTS
Forty-three patients (median age, 51 years) from 14 medical centers in Korea were analyzed, none of which were infected with human immunodeficiency virus. The majority of patients had advanced diseases, and 24 patients achieved a complete response (75.0%). After a median follow-up period of 20.0 months, 2-year event-free and overall survival rates were 70.9% and 81.4%, respectively. Eleven patients (25.6%) were unable to complete the R-hyper-CVAD regimen, including six patients due to early death. The RDIs of adriamycin, vincristine, methotrexate, and cytarabine were between 60% and 65%, which means less than 25% of patients received greater than 80% of the planned dose of each drug. Poor performance status was related to the lower RDIs of doxorubicin and methotrexate.
CONCLUSION
R-hyper-CVAD showed excellent treatment outcomes in patients who were suitable for dose-intense chemotherapy. However, management of patients who are intolerant to a dose-intense regimen remains problematic due to the frequent occurrence of treatmentrelated complications.

Keyword

Burkitt lymphoma; Rituximab; CVAD protocol

MeSH Terms

Adult
Burkitt Lymphoma
Cytarabine
Doxorubicin
Drug Therapy
Follow-Up Studies
HIV
Humans
Korea
Lymphoma*
Methotrexate
Retrospective Studies
Survival Rate
Vincristine
Cytarabine
Doxorubicin
Methotrexate
Vincristine

Figure

  • Fig. 1. Kaplan-Meier curves of time to progression, event-free survival, and overall survival of the analyzed patients.


Cited by  1 articles

The Consortium for Improving Survival of Lymphoma (CISL): recent achievements and future perspective
Cheolwon Suh, Byeong-Bae Park, Won Seog Kim
Blood Res. 2017;52(1):3-6.    doi: 10.5045/br.2017.52.1.3.


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