SWOG S1826 is an open-label trial that enrolled patients with newly diagnosed stage III or IV classical Hodgkin lymphoma who were randomly assigned to receive either nivolumab/AVD or brentuximab vedotin/AVD.
Patients with advanced-stage classical Hodgkin lymphoma (cHL) who were treated with nivolumab (Opdivo) plus doxorubicin, vinblastine, and dacarbazine (AVD) experienced progression-free survival (PFS) benefit vs brentuximab vedotin (Adcetris)/AVD, according to data from the phase 3SWOG S1826 trial (NCT03907488) that were shown during the 2023 American Society of Clinical Oncology (ASCO) Annual Meeting.
At a median follow-up of 12.1 months, results showed that patients who received nivolumab plus AVD (n = 489) experienced a 1-year estimated PFS rate of 94% (95% CI, 91%-96%) compared with 86% (95% CI, 82%-90%) among patients treated with brentuximab vedotin plus AVD (n = 487; HR, 0.48; 99% CI, 0.27-0.87; 1-sided log-rank P = .0005). Importantly, nivolumab plus AVD improved PFS compared with brentuximab vedotin plus AVD across subgroups.
“At the second planned interim analysis, the primary PFS end point crossed the protocol-specified statistical boundary, signifying that the trial had met its primary end point,” Alex F. Herrera, MD, an associate professor in the Division of Lymphoma of the Department of Hematology & Hematopoietic Cell Transplantation at City of Hope in Duarte, California, said. “Nivolumab/AVD reduced the risk of disease progression or death by [approximately] half.”
To be eligible for the study, patients needed to be at least 12 years of age, have a Zubrod performance status of 2 or less, and have a left ventricular ejection fraction of at least 50%. Patients with interstitial lung disease or pneumonitis, active autoimmune disease, or peripheral neuropathy of grade 2 or greater severity were excluded. HIV-positive patients were eligible if their disease was controlled.
SWOG S1826 was an open-label trial that enrolled patients with newly diagnosed stage III or IV cHL. Patients were randomly assigned 1:1 to receive either nivolumab at 240 mg on days 1 and 15 or brentuximab vedotin at 1.2 mg/kg on days 1 and 15. Both arms also received AVD on days 1 and 15, and treatment lasted for 6 cycles in each arm. Granulocyte colony–stimulating factor (G-CSF) use was optional in the nivolumab arm and required in the brentuximab vedotin arm.
Patients were stratified by age (12-17 vs 18-60 vs > 60), International Prognostic Score (IPS; 0-3 vs 4-7), and if end-of-treatment radiotherapy was intended (yes vs no). The primary end point was PFS. Secondary end points included event-free survival (EFS), overall survival (OS), complete response rate, and patient-reported outcomes.
Baseline patient characteristics were well-balanced between the 2 arms; the median ages were 27 years (range, 12-83) and 26 years (range, 12-81) in the nivolumab and brentuximab vedotin arms, respectively. Most patients in both arms were white (77% vs 75%), had stage IV disease (62% vs 65%), and had an International Prognostic Score (IPS) of 0 to 3 (68% vs 68%). Additionally, a majority of patients in both arms were men (55% vs 56%) and had B symptoms present (58% vs 56%).
“SWOG S1826 was a representative trial,” Herrera said. “A quarter of patients were under the age of 18 [years, and] 10% of patients were over the age of 60 [years]. A quarter of patients were Hispanic or Black. We had quite good representation from higher-risk clinical subgroups, more so than in [other] modern trials. This was a real-world trial. That’s the strength of the cooperative groups, you can enroll patients from all over the country out in the community.”
Additional findings revealed that the estimated 1-year EFS rates were 91% (95% CI, 80%-88%) vs 84% (95% CI, 80%-88%) in the nivolumab and brentuximab vedotin arms, respectively (HR, 0.56; 95% CI, 0.33-0.95; 1-sided log-rank P = .0019). The 1-year OS rates were 99% (95% CI, 98%-100%) vs 98% (95% CI, 96%-99%), respectively.
Subgroup efficacy data showed that the PFS benefit with nivolumab plus AVD over brentuximab vedotin plus AVD was consistent across subgroups, including age, IPS, and disease stage. The benefit was most pronounced among patients over 60 years of age (HR, 0.27; 95% CI, 0.10-0.76; P = .013), those with an IPS of 4 to 7 (HR, 0.40; 95% CI, 0.19-0.84; P = .015), and those with stage IV disease (HR, 0.44; 95% CI, 0.26-0.75; P = .003).
Safety findings from the study revealed that the most common any-grade adverse effects (AEs) in the nivolumab arm (n = 483) included neutropenia (55%), increased alanine transaminase (32%), and sensory neuropathy (29%). These AEs occurred at any-grade at rates of 32%, 41%, and 55%, respectively, in the brentuximab vedotin arm (n = 473).
In the nivolumab arm, grade 3 or higher AEs included neutropenia (47%), anemia (6%), and thrombocytopenia (2%). These AEs occurred at grade 3 or greater severity in the brentuximab vedotin arm at rates of 25%, 9%, and 3%, respectively.
Infectious toxicity, peripheral neuropathy, and immune-related toxicities were all AEs of special interest. Febrile neutropenia (5%), sepsis (2%), and infections/infestations (5%) were present sparingly in the nivolumab arm. These toxicities occurred at rates of 7%, 3%, and 8%, respectively, in the brentuximab vedotin arm.
Peripheral sensory neuropathy (29%) and peripheral motor neuropathy (4%) of any grade were reported in the nivolumab arm; the grade 3 or higher incidence of these events was 1% and 0%, respectively. In the brentuximab vedotin arm, rates of any-grade peripheral sensory neuropathy and peripheral motor neuropathy were 55% and 7%, respectively, and the grade 3 or higher rates for these AEs were 8%, and 1%, respectively.
G-CSF was received by 54% and 95% of patients in the nivolumab and brentuximab vedotin arms, respectively. Radiotherapy was given to 0.4% and 0.8% of patients, respectively.
“There was certainly more bone pain in the brentuximab vedotin arm, [which was] associated with [G-CSF] use,” Herrera said. “Most importantly though, there was no increase in infectious toxicity, even though there was more neutropenia in the nivolumab/AVD arm.”
Eleven percent of patients stopped treatment with nivolumab compared with 22% who ceased treatment with brentuximab vedotin. Reasons for discontinuation included AEs (8% vs 12%), progression/relapse (0% vs 1.4%), and death on treatment (0.4% vs 1.6%). Twenty-two and 30 patients, respectively, were still on treatment at the time of the analysis.
“SWOG S1826 was a key step towards harmonizing pediatric and adult therapy of Hodgkin lymphoma,” Herrera said. “Based on these data, nivolumab ABD is poised to be a new standard therapy for advanced stage Hodgkin lymphoma.”
Herrera AF, LeBlanc ML, Castellino SM, et al. SWOG S1826, a randomized study of nivolumab(N)-AVD versus brentuximab vedotin(BV)-AVD in advanced stage (AS) classic Hodgkin lymphoma (HL). J Clin Oncol. 2023;41(suppl 17):LBA4. doi:10.1200/JCO.2023.41.16_suppl.LBA4