Positron Emission Tomography–Adapted Therapy in Bulky Stage I/II Classic Hodgkin Lymphoma: CALGB 50801 (Alliance)

Author:

LaCasce Ann S.1ORCID,Dockter Travis2ORCID,Ruppert Amy S.3ORCID,Kostakoglu Lale4ORCID,Schöder Heiko5ORCID,Hsi Eric6ORCID,Bogart Jeffrey7ORCID,Cheson Bruce8ORCID,Wagner-Johnston Nina9,Abramson Jeremy10ORCID,Blum Kristie11ORCID,Leonard John P.12,Bartlett Nancy L.9ORCID

Affiliation:

1. Dana-Farber Cancer Institute, Boston, MA

2. Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN

3. Alliance Statistics and Data Management Center, The Ohio State University, Columbus, OH

4. University of Virginia, Charlottesville, VA

5. Memorial Sloan Kettering Cancer Center, New York, NY

6. Wake Forest University Health Sciences, Winston-Salem, NC

7. State University of New York Upstate Medical University Syracuse-Health Science Center, Syracuse, NY

8. Scientific Advisor, Lymphoma Research Foundation, New York, NY

9. Washington University School of Medicine, St Louis, MO

10. Massachusetts General Hospital Cancer Center, Boston, MA

11. The Ohio State University, Columbus, OH

12. Weill Medical College of Cornell University, New York, NY

Abstract

PURPOSE Patients with bulky stage I/II classic Hodgkin lymphoma (cHL) are typically treated with chemotherapy followed by radiation. Late effects associated with radiotherapy include increased risk of second cancer and cardiovascular disease. We tested a positron emission tomography (PET)–adapted approach in patients with bulky, early-stage cHL, omitting radiotherapy in patients with interim PET-negative (PET−) disease and intensifying treatment in patients with PET-positive (PET+) disease. METHODS Eligible patients with bulky disease (mass > 10 cm or 1/3 the maximum intrathoracic diameter on chest x-ray) received two cycles of doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) followed by interim fluorodeoxyglucose PET (PET2). Patients with PET2–, defined as 1-3 on the 5-point scale, received four additional cycles of doxorubicin, bleomycin, vinblastine, and dacarbazine. Patients with PET2+ received four cycles of escalated bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone followed by 30.6 Gy involved-field radiation. RESULTS Of 94 evaluable patients, 53% were female with median age 30 years (range, 18-58 years). Eight-five (90%) had stage II disease, including 48 (51%) with stage IIB/IIBE. Seventy-eight (78%) were PET2– and 21 (22%) were PET2+. The predominant toxicity was neutropenia, with 9% of patients developing febrile neutropenia and one developing sepsis. The primary end point of 3-year progression-free survival (PFS) was 93.1% in PET2– and 89.7% in PET2+ patients. Three-year overall survival was 98.6% and 94.4%, respectively. The estimated hazard ratio comparing PFS of patients with PET2+ and patients with PET2− was 1.03 (85% upper bound 2.38) and was significantly less than the null hypothesis of 4.1 (one-sided P = .04). CONCLUSION Our study of PET-adapted therapy in bulky stage I/II cHL met its primary goal and was associated with an excellent 3-year PFS rate of 92.3% in all patients, with the majority being spared radiotherapy and exposure to intensified chemotherapy.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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