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A Real-Life Multicenter Study of Checkpoint Inhibitors in Relapsed/Refractory Primary Mediastinal B-Cell Lymphoma
Gabriele Gugliotta1, Lisa Argnani2, Martina Cantelli2
1IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
American Journal of Hematology
|April 10, 2026
Summary
Immune checkpoint inhibitors (ICIs) show promise for relapsed or refractory primary mediastinal B-cell lymphoma (PMBCL). Long-lasting responses were observed, suggesting ICIs may offer a curative intent for some patients.
Area of Science:
- Hematology
- Oncology
- Immunotherapy
Background:
- Immune checkpoint inhibitors (ICIs) have improved outcomes for relapsed or refractory (R/R) primary mediastinal B-cell lymphoma (PMBCL).
- Real-world data on ICI efficacy and optimal consolidation strategies in R/R PMBCL are limited.
Purpose of the Study:
- To evaluate the real-world effectiveness and safety of ICIs (pembrolizumab or nivolumab-brentuximab vedotin) as salvage therapy for R/R PMBCL.
- To assess the impact of consolidation strategies on long-term outcomes in R/R PMBCL patients treated with ICIs.
Main Methods:
- Retrospective observational study (PRIMICI) of 74 R/R PMBCL patients treated with ICIs in an off-label setting.
- Patients received either pembrolizumab (42) or nivolumab-brentuximab vedotin (32).
- Median follow-up of 34 months, analyzing response rates, progression-free survival (PFS), and overall survival (OS).
Main Results:
- Overall response rate (ORR) was 64%, with a complete response (CR) rate of 50%.
- Four-year disease-free survival was 100% for patients achieving CR, irrespective of consolidation.
- Estimated 5-year PFS was 60.4% and OS was 77.5%; nivolumab-brentuximab vedotin showed superior response rates and OS compared to pembrolizumab.
Conclusions:
- Pembrolizumab and nivolumab-brentuximab vedotin are safe and effective salvage therapies for R/R PMBCL.
- Durable responses are achievable with ICIs, potentially with curative intent, regardless of consolidation strategies.
- Improved OS observed post-2020 likely due to the integration of CAR T-cell therapy as a salvage option.
Keywords:
brentuximab‐vedotinnivolumabpembrolizumabprimary mediastinal B‐cell lymphomarelapsed/refractory
