BEACOPP regimen associated with 97% OS in high-risk Hodgkin’s lymphoma

Kelly KM. Blood. 2011;117:2596-2603.

  • March 29, 2011

Results from a study of 98 children and adolescents with high-risk Hodgkin’s lymphoma show that early intensification with BEACOPP chemotherapy followed by less intense response-based therapy for rapidly responding patients was associated with high rates of event-free and overall survival.

Researchers said these results “demonstrate that early dose intensification with escalated-dose BEACOPP chemotherapy is not only feasible but highly effective.”

From October 1999 to May 2001, patients aged younger than 21 years who had been diagnosed with advanced Hodgkin’s lymphoma were assigned to four courses of induction chemotherapy with escalated-dose BEACOPP administered every 21 days. Patients who responded slowly to treatment were assigned another four more courses of escalated-dose BEACOPP followed by 21 Gy of radiotherapy. Patients with residual disease identified on imaging studies were assigned to an additional 35 Gy.

Most patients (57%) had stage IV disease and the majority presented with high-risk features including B-symptoms (70%), hilar adenopathy (73%), nodal aggregate greater than 10 cm (61%) and three or more nodal regions involved (74%). Sixty-four patients had bulk disease at diagnosis.

Median follow-up among patients with no reported event was 6.3 years and 91% of patients were followed for a minimum of 3 years. Five-year event-free survival was 94% ± 2.4%. Five-year OS was 97% ± 1.9%.

Neutropenia (83%), anemia (79%) and thrombocytopenia (62%) were the most common grade-3/grade-4 toxicities. Stomatitis, dysphagia, esophagitis and odynophagia were the most common non-hematologic toxicities reported.

PERSPECTIVE

Cindy Schwartz, MD
Cindy Schwartz

We certainly know the BEACOPP regimen is effective. What we’re trying to do now is avoid using so much of the alkylator, and find children who may not need so much doxorubicin which affects for the heart. We know BEACOPP works, we know it’s a maximal therapy. For the vast majority of patients, we can probably come up with less therapy and something that works faster. These results present a wonderful outcome that is not compared anywhere else and our hope is that we can continue to tailor therapy so that we can get these sorts of outcomes across the board by knowing exactly who needs the extra therapy.

– Cindy Schwartz, MD
Director of Pediatric Hematology/Oncology
Hasbro Children's Hospital in Providence, RI

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