Targeted radiotherapy for early-stage, low-risk pediatric Hodgkin lymphoma slow early responders: a COG AHOD0431 analysis

Author:

Parekh Akash1ORCID,Keller Frank G.2,McCarten Kathleen M.3,Kessel Sandy3,Cho Steve4,Pei Qinglin5,Wu Yue5,Castellino Sharon M.2,Constine Louis S.6,Schwartz Cindy L.7,Hodgson David8ORCID,Kelly Kara M.9,Hoppe Bradford S.10ORCID

Affiliation:

1. 1Department of Radiation Oncology, University of Florida, Gainesville, FL;

2. 2Aflac Cancer and Blood Disorders Center, Children’s Healthcare of Atlanta and Emory University, Atlanta, GA;

3. 3Imaging and Radiation Oncology Core, Lincoln, RI;

4. 4Nuclear Medicine Section, Department of Radiobiology, University of Wisconsin Carbone Comprehensive Cancer Center, Madison, WI;

5. 5Department of Biostatistics, University of Florida College of Public Health and Health Professions and College of Medicine, Gainesville, FL;

6. 6Departments of Radiation Oncology and Pediatrics, University of Rochester Medical Center, Rochester, NY;

7. 7Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI;

8. 8Department of Radiation Oncology, University of Toronto, Toronto, ON, Canada;

9. 9Department of Pediatrics, Roswell Park Comprehensive Cancer Center, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, NY; and

10. 10Department of Radiation Oncology, Mayo Clinic, Jacksonville, FL

Abstract

Abstract Children’s Oncology Group (COG) trial AHOD0431 reduced systemic therapy and used response-adapted involved-field radiotherapy (IFRT) in early-stage pediatric classic Hodgkin lymphoma. We investigated the impact of positron emission tomographic response after 1 cycle (PET1) and on IFRT outcomes and pattern of relapse. Patients in AHOD0431 underwent PET1 response assessment after AVPC (doxorubicin, vincristine, prednisone, and cyclophosphamide). “Rapid early responders” (RERs) had a negative PET1 (PET1−); “slow early responders” (SERs) had a positive PET1 (PET1+). Patients with a partial response by computed tomographic and functional imaging after 3 chemotherapy cycles received 21-Gy IFRT, whereas complete responders had no IFRT. Progression-free survival (PFS) was evaluated for RERs and SERs treated with or without IFRT. Recurrence sites were initial, new, or both. Relapses involving initial sites were characterized as “within the PET1+ site” or “initially involved but outside the PET1+ site.” Median follow-up was 118 months. The 10-year PFS rate among RERs was 96.6% with IFRT and 84.1% without IFRT (P = .10), whereas SERs were 80.9% with IFRT and 64.0% without IFRT (P = .03). Among 90 RERs who did not receive IFRT, all 14 relapses included an initial site. Among 45 SERs receiving no IFRT, 14 of 16 relapses were in the initial site (9 PET1+ site only). Among 58 patients receiving IFRT, 5 of 10 relapses were in the PET1+ site. After 3 cycles of AVPC alone, RERs showed favorable results. Conversely, SERs had unfavorable outcomes with AVPC alone, although they improved with 21-Gy IFRT. RT remains an important component of treatment for SERs. This trial was registered at www.clinicaltrials.gov as #NCT00302003.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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