Efficacy and safety of orelabrutinib combined with sintilimab in patients with relapsed/refractory primary central nervous system lymphoma: a prospective multicenter phase ii study

Relapsed or refractory primary central nervous system lymphoma (R/R PCNSL) has a poor prognosis, with limited effective salvage treatments. Bruton tyrosine kinase inhibitors (BTKis) showed considerable efficacy, although the duration of effect was unsatisfactory. Orelabrutinib, a new, highly selective BTK inhibitor, has demonstrated an improved ability to cross the blood-brain barrier. PD-1 inhibitors demonstrate efficacy in the treatment of PCNSL. The combination of BTK inhibitors with PD-1 blockade produces synergistic effects. BTK inhibition suppresses tumor proliferation, promotes T-cell infiltration, and reverses T-cell exhaustion, thereby enhancing the effectiveness of PD-1. This phase II study aims to evaluate the efficacy and safety of this combination in R/R PCNSL. This prospective, multicenter, single-arm phase II study (NCT04899427) enrolled 28 consecutive patients with R/R PCNSL who received orelabrutinib combined with sintilimab between March 2021 and October 2023. The primary endpoint was the overall response rate (ORR) after 4 treatment cycles. Secondary endpoints included 1-year progression-free survival (PFS), overall survival (OS), duration of response (DOR), and safety. The median age was 61.0 years, with 92.9% experiencing relapse and 7.1% having refractory disease. Among 28 evaluable patients, the ORR after 4 cycles was 60.7% (17/28), including 8 (28.6%) with complete responses, 2 (7.1%) with unconfirmed complete responses, and 7 (25.0%) with partial responses. The median PFS was 8.4 months; the 1- and 2-year PFS rates were 49.7% and 40.7%, respectively. Median OS was not reached, with 1- and 2-year OS rates of 77.4% and 73.3%. The median DOR was notably prolonged at 42.4 months. The combination of orelabrutinib and sintilimab was well tolerated. Treatment-emergent adverse events (TEAEs) of any grade occurred in 75.0% (21/28) of patients, with 71.4% (20/28) experiencing grade 1-2 events and 14.3% (4/28) experiencing grade 3-4 events. One grade 5 event (COVID-19 infection) was reported. No immune-related adverse events occurred. This prospective phase II study showed that combining orelabrutinib with sintilimab provided significant clinical benefits for patients with R/R PCNSL, including high response rates and notably durable responses. The manageable safety profile further supports this combination as a valuable treatment option for this challenging population. ClinicalTrials.gov NCT04899427. Last Update Posted: May 24, 2021.

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BMC Cancer
Published
2026-10-28
DOI
https://doi.org/10.1186/s12885-026-17092-x
Primary Topic
CNS Lymphoma Diagnosis and Treatment
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article
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article

Efficacy and safety of orelabrutinib combined with sintilimab in patients with relapsed/refractory primary central nervous system lymphoma: a prospective multicenter phase ii study

阮净, Chong Wei, Hui Liu, Daobin Zhou et al.
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BMC Cancer
CNS Lymphoma Diagnosis and Treatment
article

Efficacy and safety of orelabrutinib combined with sintilimab in patients with relapsed/refractory primary central nervous system lymphoma: a prospective multicenter phase ii study

阮净, Chong Wei, Hui Liu, Daobin Zhou, Jie Ma, Yan Zhang, Danqing Zhao, Wei Zhang
article en

Abstract

Relapsed or refractory primary central nervous system lymphoma (R/R PCNSL) has a poor prognosis, with limited effective salvage treatments. Bruton tyrosine kinase inhibitors (BTKis) showed considerable efficacy, although the duration of effect was unsatisfactory. Orelabrutinib, a new, highly selective BTK inhibitor, has demonstrated an improved ability to cross the blood-brain barrier. PD-1 inhibitors demonstrate efficacy in the treatment of PCNSL. The combination of BTK inhibitors with PD-1 blockade produces synergistic effects. BTK inhibition suppresses tumor proliferation, promotes T-cell infiltration, and reverses T-cell exhaustion, thereby enhancing the effectiveness of PD-1. This phase II study aims to evaluate the efficacy and safety of this combination in R/R PCNSL. This prospective, multicenter, single-arm phase II study (NCT04899427) enrolled 28 consecutive patients with R/R PCNSL who received orelabrutinib combined with sintilimab between March 2021 and October 2023. The primary endpoint was the overall response rate (ORR) after 4 treatment cycles. Secondary endpoints included 1-year progression-free survival (PFS), overall survival (OS), duration of response (DOR), and safety. The median age was 61.0 years, with 92.9% experiencing relapse and 7.1% having refractory disease. Among 28 evaluable patients, the ORR after 4 cycles was 60.7% (17/28), including 8 (28.6%) with complete responses, 2 (7.1%) with unconfirmed complete responses, and 7 (25.0%) with partial responses. The median PFS was 8.4 months; the 1- and 2-year PFS rates were 49.7% and 40.7%, respectively. Median OS was not reached, with 1- and 2-year OS rates of 77.4% and 73.3%. The median DOR was notably prolonged at 42.4 months. The combination of orelabrutinib and sintilimab was well tolerated. Treatment-emergent adverse events (TEAEs) of any grade occurred in 75.0% (21/28) of patients, with 71.4% (20/28) experiencing grade 1-2 events and 14.3% (4/28) experiencing grade 3-4 events. One grade 5 event (COVID-19 infection) was reported. No immune-related adverse events occurred. This prospective phase II study showed that combining orelabrutinib with sintilimab provided significant clinical benefits for patients with R/R PCNSL, including high response rates and notably durable responses. The manageable safety profile further supports this combination as a valuable treatment option for this challenging population. ClinicalTrials.gov NCT04899427. Last Update Posted: May 24, 2021.

BMC Cancer
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking Union Medical College Hospital (CN), Zhengzhou University (CN), Beijing Hospital (CN), First Affiliated Hospital of Zhengzhou University (CN)
Good health and well-being
Openalex Percentile: Top 14%
CNS Lymphoma Diagnosis and Treatment
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