BEACOPP chemotherapy is a highly effective regimen in children and adolescents with high-risk Hodgkin lymphoma: a report from the Children's Oncology Group

Author:

Kelly Kara M.1,Sposto Richard23,Hutchinson Raymond4,Massey Vickie5,McCarten Kathleen6,Perkins Sherrie7,Lones Mark8,Villaluna Doojduen9,Weiner Michael1

Affiliation:

1. Division of Pediatric Oncology, Columbia University Medical Center, New York, NY;

2. Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA;

3. Children's Center for Cancer and Blood Diseases, Children's Hospital Los Angeles, Los Angeles, CA;

4. Division of Pediatric Hematology/Oncology, University of Michigan Medical School, Ann Arbor, MI;

5. Children's Mercy Hospital, Kansas City Cancer Center, Overland Park, KS;

6. Departments of Diagnostic Imaging and Pediatrics, Warren Alpert Medical School, Brown University, and Rhode Island Hospital, Providence, RI;

7. University of Utah and ARUP Laboratories, Department of Pathology, Salt Lake City, UT;

8. Pathology Department, Children's Hospital of Orange County/St Joseph Hospital, Orange, CA; and

9. Children's Oncology Group, Arcadia, CA

Abstract

AbstractDose-intensified treatment strategies for Hodgkin lymphoma (HL) have demonstrated improvements in cure but may increase risk for acute and long-term toxicities, particularly in children. The Children's Oncology Group assessed the feasibility of a dose-intensive regimen, BEACOPP (bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, prednisone) in children with high-risk HL (stage IIB or IIIB with bulk disease, stage IV). Rapidity of response was assessed after 4 cycles of BEACOPP. Rapid responders received consolidation therapy with guidelines to reduce the risk of sex-specific long-term toxicities of therapy. Females received 4 cycles of COPP/ABV (cyclophosphamide, vincristine, procarbazine, prednisone, doxorubicin, bleomycin, vinblastine) without involved field radiation therapy (IFRT). Males received 2 cycles of ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine) with IFRT. Slow responders received 4 cycles of BEACOPP and IFRT. Ninety-nine patients were enrolled. Myelosuppression was frequent. Rapid response was achieved by 74% of patients. Five-year event-free-survival is 94%, IFRT with median follow-up of 6.3 years. There were no disease progressions on study therapy. Secondary leukemias occurred in 2 patients. Overall survival is 97%. Early intensification followed by less intense response-based therapy for rapidly responding patients is an effective strategy for achieving high event-free survival in children with high-risk HL. This trial is registered at http://www.clinicaltrials.gov as #NCT00004010.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference35 articles.

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