Extending anti-PD-1–based options in the setting of Hodgkin lymphoma

Patients with relapsed or refractory classical Hodgkin lymphoma (cHL) who have failed high-dose chemotherapy and autologous stem cell transplantation (HDT/ASCT) have poor prognosis, which also applies to those with chemotherapy-resistant disease who are ineligible for HDT/ASCT [1-4]. The presence of chromosome 9p24.1 alterations in cHL provides a rationale for immune checkpoint inhibition as this leads to overexpression of the PD-L1 ligands [5-7]. Anti-PD-1 antibodies including nivolumab, pembrolizumab, tislelizumab, camrelizumab and sintilimab have changed the treatment paradigm of adults with relapsed/refractory cHL [8-14]. Data presented at ASCO, EHA and ICML 2021 demonstrated efficacy of new agents and established PD-1 inhibitors over extended periods of time.

CheckMate 205

The pivotal, multicenter, single-arm, phase II CheckMate 205 trial evaluated the PD-1 inhibitor nivolumab at a dose of 3 mg/kg 2-weekly in patients with relapsed/refractory cHL after ASCT failure in three cohorts. Cohort A included 63 brentuximab vedotin(BV)-naïve patients; those in Cohort B (n = 80) had received BV after ASCT, while those in Cohort C (n = 100) had been treated with BV before and/or after ASCT. Objective response rate (ORR) by independent review committee (IRC) was defined as the primary endpoint. In Cohort C, patients who achieved complete remission (CR) for ≥ 1 year could discontinue treatment and receive re-treatment if relapses occurred within two years.

At the time of the 33-month follow-up presented at the ASH 2018 Congress, the ORR was 71 %, with 21 % of patients obtaining CR [15]. Ansell et al. reported updated results from CheckMate 205 with a median follow-up of 58 months at ICML 2021 [16]. Median duration of treatment was 14 months in the entire cohort. In 24 %, patients had been able to receive subsequent hematopoietic stem cell transplant based on the benefit from the study treatment.

Response-related outcome improvements

The 5-year follow-up confirmed the efficacy and safety of nivolumab in patients with cHL who have progressed or relapsed after ASCT. ORRs were 65 %, 71 % and 75 % for Cohorts A, B and C, respectively. Complete remissions resulted in 32 %, 14 % and 21 %, respectively. The CR rate in the total population had increased from 16 % at 33 months to 21 % at 58 months. Remissions proved durable, particularly in patients who had obtained CR; here, the median duration of response was 30.3 months compared to 13.5 months in the group with partial remission (PR). Favorable overall survival (OS) results were observed over time. At 5 years, 71.4 % of all patients were alive, and median OS had not been reached in the groups with CR, PR, and stable disease, with those in the CR cohort showing the best survival outcome (Figure). Even in the group that progressed during the study and received salvage therapies, many patients survived.

The 5-year progression-free survival (PFS) rate in the total population amounted to 18 %, with median PFS of 15.1 months. Median PFS was longest in the CR cohort (37.4 months); this was more than double the result seen for patients with PR (15.2 months).

The adverse event (AE) profile resembled the findings reported previously. No new safety signals or increases in toxicity were noted over time. Any-grade serious treatment-related AEs (TRAEs) occurred in 15 %, and the treatment was discontinued due to TRAEs in 11 %. Immune-related AEs (irAEs) were mainly classified as grade 1 or 2. Rash occurred most frequently (12 %), followed by hepatitis (6 %), and pneumonitis (6 %). Overall, these proportions were relatively modest despite the patients being on treatment for a long time.

In Cohort C, 12 patients out of 100 discontinued nivolumab therapy after they had maintained CR for ≥ 1 year. Among these, six remained in CR with no additional intervention. Four of the other six patients experienced disease progression. Three were re-treated per protocol, with one continuing on treatment and being in remission at the time of the analysis. In their summary, the authors pointed out that it appears feasible to stop nivolumab therapy after one year of CR and to re-initiate treatment upon disease progression.

Figure: Overall survival by best response obtained with nivolumab in CheckMate 205

Figure: Overall survival by best response obtained with nivolumab in CheckMate 205

BGB-A317-203: tislelizumab

Optimized efficacy can be expected from the PD-1 inhibitor tislelizumab that was engineered to minimize binding to FcγR on macrophages, which compromises anti-tumor activity of PD-1 antibodies through activation of antibody-dependent macrophage-mediated killing of effector T cells [17, 18]. The pivotal, multicenter, single-arm, phase II BGB-A317-203 trial tested tislelizumab 200 mg i. v. every 3 weeks in 70 patients with relapsed/refractory cHL who were ineligible for intensive treatment after ≥ 2 lines of systemic therapy or had achieved no response or progressed after HDT/ASCT. All patients had received chemotherapy; immunotherapy and BV had been administered in 21.4 % and 5.7 %, respectively. Nineteen percent had undergone ASCT, while the remaining patients were no candidates for transplant. The ORR by IRC constituted the primary endpoint. Song et al. presented long-term data at EHA 2021 [19].

After a follow-up of 33.8 month, tislelizumab proved highly active. Objective responses occurred in 87.1 %, and CRs were achieved by 67.1 % of patients. Complete remissions emerged irrespective of the number of prior treatment lines and pretreatment with ASCT or BV (Table 1). The median time to response was 12 weeks, with 72 % of complete responders obtaining CR at the first post-baseline tumor assessment. Median PFS was 31.5 months. At the time of the 36-month landmark analysis, 40.8 % of patients remained progression-free. Patients who had achieved CR fared better in terms of PFS compared to those with PR and stable disease (not reached vs. 13.2 months). The OS results were immature; at 36 months, 84.8 % of patients lived, which is favorable considering the relapsed/refractory disease setting.

Grade ≥ 3 TRAEs occurred in 31.4 %, and in 8.6 %, AEs necessitated treatment discontinuation. irAEs were observed in 45.7 % and mainly included hypothyroidism (28.6 %), skin reactions (8.6 %), and pneumonitis (7.1 %). No new safety concerns were identified. In their summary, the authors noted that tislelizumab conferred a favorable benefit-risk profile and might represent an important treatment option for patients with relapsed or refractory cHL. A confirmatory phase III study is ongoing.

able 1 Responses to tislelizumab monotherapy irrespective of pretreatment

Update on camrelizumab

Camrelizumab has been approved in China based on the primary results of a multicenter, phase II trial in 75 patients with relapsed/refractory cHL in whom ASCT had failed to induce (lasting) remission or who had received ≥ 2 lines of systemic chemotherapies. The primary analysis yielded IRC-assessed objective responses in 76 % of patients, including CR in 28.0 % [14]. Follow-up data presented at EHA 2021 after 36.2 months demonstrated an ORR of 76.0 % by IRC assessment, with 26.7 % of patients experiencing CR [20]. Overall, 94.7 % achieved disease control. More than half showed ongoing responses at the time of the analysis. Median duration of response and median PFS were 31.7 and 22.5 months, respectively. Median OS had not been reached yet; at 36 months, 82.7 % of patients were alive.

The most common AE was cutaneous reactive capillary endothelial proliferation (RCEP) that occurred in almost all patients but was classified exclusively as grade 1 or 2. Complete resolution of RCEP lesions occurred in 67.1 %, with median time to complete resolution of 8.2 months. Most of the RCEP lesions regressed spontaneously, and none required systemic corticosteroids. At 12 and 24 months, the recurrence rates were 19.0 % and 6.3 %, respectively. No new toxicities emerged during the prolonged follow-up. AEs led to treatment interruption and discontinuation in 40.0 % and 6.7 %, respectively. The authors concluded that camrelizumab monotherapy continued to provide robust and durable responses as well as favorable survival and a manageable safety profile.

Promising results for penpulimab

Penpulimab is a novel IgG1 anti-PD-1 antibody engineered to eliminate binding to FcγRIa and FcγRIIIa receptors with the aim to avoid or reduce antibody-dependent cellular cytotoxicity, antibody-dependent cellular phagocytosis, and antibody-dependent cytokine release. A multicenter, single-arm, open-label, phase I/II study investigated penpulimab 200 mg i. v. 2-weekly in patients with relapsed/refractory cHL following ASCT or ≥ 2 lines of chemotherapy. Updated phase II findings from the trial were presented at ASCO 2021 for 94 and 85 patients included in the safety and full analysis sets, respectively [25]. Almost 65 % of patients in the full analysis set had stage IV disease, and ≥ 3 prior lines of therapy had been administered in more than half of cases.

Among 85 evaluable patients, ORR with penpulimab was 89.4 %, and 47.1 % achieved CR (Table 2). The ORR benefit prevailed in all evaluated subgroups. Median duration of response had not been reached, which also applied to median PFS and median OS. All patients were alive at 18 months. The most frequent TRAEs included hypothy­roidism (31.9 %), upper respiratory tract infection (25.5 %), fever (24.5 %) and alanine aminotransferase elevations (23.4 %). Grade 3 TRAEs were observed in 26.6 %, and treatment was discontinued in 5.3 %. Penpulimab showed a favorable immune-related safety profile. Grade 3 events occurred in 4.3 %, and no patient developed grade 4/5 events. Excluding thyroid disease, irAEs were reported in 17.0 % of the population.

Table 2 Efficacy outcomes observed for penpulimab in the evaluable patient population

Chidamide in addition to decitabine/camrelizumab

The combination of the anti-PD-1 antibody camrelizumab with the DNA-demethylating agent decitabine was evaluated in the clinical trial setting based on the observation that inhibition of de novo methylation can increase T-cell responses and tumor control during PD-1 inhibitor therapy in mice [21, 22]. Indeed, in a randomized phase II trial, camrelizumab plus decitabine elicited CRs in 79 % of patients with relapsed/refractory cHL, compared to 32 % with camrelizumab alone (p = 0.001) [23]. However, effective options have been lacking for patients who progressed on this regimen. A phase II study therefore tested a combined approach encompassing the histone deacetylase inhibitor chidamide in patients with relapsed/refractory cHL who had progressed or relapsed on camrelizumab/decitabine. Nineteen patients were treated with chidamide 10 mg (days 1–4) and 20 mg (days 8, 11,15, 18) plus decitabine 10 mg (days 1–5) and camrelizumab 200 mg (day 6) every 3 weeks.

According to preliminary results reported at ASCO 2021, the triple combination induced pronounced responses and showed an acceptable safety profile [24]. Among 14 patients who completed the response evaluation, 13 (93 %) experienced objective responses, including CRs in six cases (43 %). The most common AEs were leukopenia (58 %; grade 3, 16 %), nausea (53 %) and hypertriglyceridemia (26 %). No irAEs occurred.


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