Patterns of progression after immune checkpoint inhibitors for Hodgkin lymphoma: implications for radiation therapy

Author:

Burlile Jessica F.1ORCID,Frechette Kelsey M.1,Breen William G.1,Hwang Steven R.2ORCID,Higgins Alexandra S.2,Nedved Adrienne N.3,Harmsen William S.4,Pulsipher Sydney D.4ORCID,Witzig Thomas E.2ORCID,Micallef Ivana N.2,Hoppe Bradford S.5ORCID,Habermann Thomas M.2,Thanarajasingam Gita2,Johnston Patrick B.2,Inwards David J.2,Bennani N. Nora2ORCID,Peterson Jennifer L.5ORCID,Stish Bradley J.1,Rule William G.6,Ansell Stephen M.2,Lester Scott C.1

Affiliation:

1. 1Department of Radiation Oncology, Mayo Clinic, Rochester, MN

2. 2Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN

3. 3Department of Pharmacy, Mayo Clinic, Rochester, MN

4. 4Department of Biostatistics and Health Sciences Research, Mayo Clinic, Rochester, MN

5. 5Department of Radiation Oncology, Mayo Clinic, Jacksonville, FL

6. 6Department of Radiation Oncology, Mayo Clinic, Phoenix, AZ

Abstract

Abstract Immune checkpoint inhibitors (ICIs) have demonstrated remarkable response rates in relapsed or refractory Hodgkin lymphoma (HL). Still, most patients eventually progress. Patterns of progression after ICIs are not well described and are essential to defining the role of local therapies in combination with ICIs. We identified patients who received ICIs for HL between 2013 and 2022. Fludeoxyglucose-18 positron emission tomography (FDG-PET) before initiating ICI and at progression on/after ICI were reviewed, and areas of active HL were recorded. An exploratory analysis of treatable progression included patients with ≤5 sites of disease on pre-ICI FDG-PET and progression only at pre-ICI sites. Ninety patients were identified; 69 had complete records, and of these, 32 (52%) had relapsed at ICI initiation, 17 (25%) were refractory, and 16 (23%) received ICI as first-line therapy. Forty-five of 69 patients had ≤5 sites of disease (limited) on pre-ICI FDG-PET. Patients with >5 sites of disease had a higher risk of progression, and every site of disease >5 sites conferred an additional 1.2x higher chance of progression. At a median follow-up of 4.0 years, 41 of 69 patients had progressed on/after ICIs (cumulative incidence 66.4%), and of these, 22 of 41 patients progressed only at pre-ICI sites (cumulative incidence 39.4%). In an exploratory analysis, the cumulative incidence of a treatable progression among 45 patients with limited disease was 34%. The cumulative incidence of any progression among this cohort was 58.9%. More than one-third of patients with limited disease before ICIs experienced progression only at pre-ICI sites of disease. These patients could be candidates for radiation during or after ICIs.

Publisher

American Society of Hematology

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