TY - JOUR
T1 - Yttrium-90-Ibritumomab Tiuxetan (Zevalin®) Radioimmunotherapy after Cytoreduction with ESHAP Chemotherapy in Patients with Relapsed Follicular Non-Hodgkin Lymphoma
T2 - Final Results of a Phase II Study
AU - Puvvada, Soham D.
AU - Guillén-Rodríguez, José M.
AU - Yan, Jessica
AU - Inclán, Lora
AU - Heard, Kara
AU - Rivera, Xavier I.
AU - Anwer, Faiz
AU - Mahadevan, Daruka
AU - Schatz, Jonathan H.
AU - Persky, Daniel O.
N1 - Funding Information:
Research funding for this study was received from Spectrum Pharmaceuticals. The research reported in this publication was supported by the National Cancer Institute of the National Institutes of Health (award No. P30 CA023074).
Publisher Copyright:
© 2018 S. Karger AG, Basel.
PY - 2018/4/1
Y1 - 2018/4/1
N2 - 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.
AB - 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.
KW - CD20
KW - Follicular lymphoma
KW - Indolent non-Hodgkin lymphoma
KW - Phase II trial
KW - Relapsed/refractory lymphoma
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UR - http://www.scopus.com/inward/citedby.url?scp=85042373242&partnerID=8YFLogxK
U2 - 10.1159/000486788
DO - 10.1159/000486788
M3 - Article
C2 - 29471300
AN - SCOPUS:85042373242
SN - 0030-2414
VL - 94
SP - 274
EP - 280
JO - Oncology (Switzerland)
JF - Oncology (Switzerland)
IS - 5
ER -