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DOI 10.1056/nejmoa1308392

Медицинская библиотека · The New England journal of medicine · 2013

Low-intensity therapy in adults with Burkitt's lymphoma.

Dunleavy Kieron, Pittaluga Stefania, Shovlin Margaret, Steinberg Seth M, Cole Diane, Grant Cliona, Widemann Brigitte, Staudt Louis M, Jaffe Elaine S, Little Richard F, Wilson Wyndham H

Клиническое исследованиеСтатьяПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

BACKGROUND

Burkitt's lymphoma is an aggressive B-cell lymphoma that occurs in children and adults and is largely curable with the use of intensive and toxic chemotherapy. Current treatments are less effective and have more severe side effects in adults and patients with immunodeficiency than in children.

METHODS

We studied low-intensity treatment consisting of infused etoposide, doxorubicin, and cyclophosphamide with vincristine, prednisone, and rituximab (EPOCH-R) in patients with untreated Burkitt's lymphoma. Two EPOCH-R regimens were tested: a standard dose-adjusted combination in human immunodeficiency virus (HIV)-negative patients (DA-EPOCH-R group) and a lower-dose short-course combination with a double dose of rituximab in HIV-positive patients (SC-EPOCH-RR group).

RESULTS

A total of 30 consecutive patients were treated; 19 patients were in the DA-EPOCH-R group, and 11 in the SC-EPOCH-RR group. The overall median age of the patients was 33 years, and 40% were 40 years of age or older; 73% of the patients had intermediate-risk disease, and 10% had high-risk disease. The principal toxic events, fever and neutropenia, were observed during 22% of the DA-EPOCH-R treatment cycles and 10% of the SC-EPOCH-RR treatment cycles. The tumor lysis syndrome developed in 1 patient; no treatment-related deaths occurred. The median cumulative doses of doxorubicin-etoposide and cyclophosphamide administered in the SC-EPOCH-RR group were 47% and 57% lower, respectively, than those administered in the DA-EPOCH-R group. With median follow-up times of 86 months in the DA-EPOCH-R group and 73 months in the SC-EPOCH-RR group, the rates of freedom from progression of disease and overall survival were, respectively, 95% and 100% with DA-EPOCH-R and 100% and 90% with SC-EPOCH-RR. None of the patients died from Burkitt's lymphoma.

CONCLUSIONS

In this uncontrolled prospective study, low-intensity EPOCH-R-based treatment was highly effective in adults with sporadic or immunodeficiency-associated Burkitt's lymphoma. (Funded by the National Cancer Institute; ClinicalTrials.gov numbers, NCT00001337 and NCT00006436.).

Для цитирования: Dunleavy Kieron, Pittaluga Stefania, Shovlin Margaret, Steinberg Seth M, Cole Diane, Grant Cliona, Widemann Brigitte, Staudt Louis M, Jaffe Elaine S, Little Richard F, Wilson Wyndham H. Low-intensity therapy in adults with Burkitt's lymphoma.. The New England journal of medicine. 2013. DOI: 10.1056/nejmoa1308392.

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