Background: Radioimmunotherapy (RIT) is effective in treating relapsed/refractory follicular lymphoma (FL), with durable remissions in first-line consolidation. We hypothesized that RIT with ibritumomab tiuxetan (Zevalin®) would result in durable remissions by eliminating minimal residual disease after cytoreduction.

Methods: Patients with FL received 2 cycles of ESHAP (etoposide, methylprednisolone, cytarabine, cisplatin) every 28 days, followed by Zevalin 4-6 weeks later if there was no disease progression and bone marrow biopsy showed < 25% involvement.

Results: Twenty-eight patients were treated, with a median age of 61 years, median of 3 prior therapies, 49% high-risk disease (Follicular Lymphoma International Prognostic Index, FLIPI), and 39% progressive disease. Three patients did not receive Zevalin due to residual bone marrow involvement. The main toxicities were cytopenias, with 11% febrile neutropenia. The overall response rate (ORR) was 72%, with 45% achieving complete response. With a median follow-up of 73 months, 1-year progression-free survival (PFS) was 38%, and median PFS was 10 months, but median overall survival (OS) was not reached.

Conclusion: The study did not reach its primary endpoint of a 1-year PFS of 67.3%. Reasons for this could include low accrual, high-risk disease, and inadequate debulking provided by 2 cycles of ESHAP. However, this protocol was associated with tolerable toxicity, high ORR, and high OS. Further studies would optimize debulking and focus on high-risk FL patients.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050637PMC
http://dx.doi.org/10.1159/000486788DOI Listing

Publication Analysis

Top Keywords

tiuxetan zevalin®
8
follicular lymphoma
8
durable remissions
8
cycles eshap
8
bone marrow
8
high-risk disease
8
patients
5
disease
5
median
5
yttrium-90-ibritumomab tiuxetan
4

Similar Publications

Recent preclinical and clinical advances in radioimmunotherapy for non-Hodgkin's lymphoma.

Explor Target Antitumor Ther

February 2024

Division of Hematopoiesis, Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto 860-0811, Japan.

Article Synopsis
  • * Two RIT agents, Zevalin and Bexxar, have been approved by the FDA for treating specific types of NHL, but their use has declined due to the rise of new therapies and complexities in administering them.
  • * New advancements in RIT include novel targets, therapeutic strategies using alpha-particle isotopes for better tumor targeting, and the development of immuno-PET imaging for personalized treatment monitoring.
View Article and Find Full Text PDF
Article Synopsis
  • The study reviews the clinical efficacy and safety of anti-CD20 radioimmunotherapy (RIT) for treating indolent B-cell lymphomas, highlighting two approved agents: 90Y-ibritumomab tiuxetan and 131I-tositumomab.
  • Numerous clinical trials support RIT's effectiveness, especially in high-risk and heavily pretreated patient populations, with manageable toxicity profiles.
  • Continued research is needed to explore long-term response biomarkers and optimize RIT within treatment strategies, as it shows promise for sustained remission and serves as a viable alternative to other therapies.
View Article and Find Full Text PDF

Patients with asymptomatic follicular lymphoma (AFL) are candidates for observation or immunotherapy. Given the effectiveness of radiation therapy in FL, another option is 90Yttrium-ibritumomab tiuxetan radioimmunotherapy (RIT). We conducted a trial where untreated AFL patients were randomized to rituximab 375 mg/m2 weekly × 4 or rituximab 250 mg/m days 1, 8, and 0.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!