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. 2022 Nov 18;14(22):5670.
doi: 10.3390/cancers14225670.

Allogeneic Hematopoietic Stem Cell Transplantation in Transformed Follicular Lymphoma (tFL): Results of a Retrospective Multicenter Study from GELTAMO/GETH-TC Spanish Groups

Affiliations

Allogeneic Hematopoietic Stem Cell Transplantation in Transformed Follicular Lymphoma (tFL): Results of a Retrospective Multicenter Study from GELTAMO/GETH-TC Spanish Groups

Beatriz Rey-Búa et al. Cancers (Basel). .

Abstract

Background: Transformation of follicular lymphoma into an aggressive lymphoma (tFL) worsens the prognosis and the standard treatment is not completely defined. Allogeneic hematopoietic stem cell transplantation (alloSCT) could be a potentially curative option for these patients, but it has not been widely explored.

Methods: We designed a retrospective multicenter study to analyze the efficacy and toxicity of alloSCT in tFL patients and potential prognostic factors of survival.

Results: A total of 43 patients diagnosed with tFL who underwent alloSCT in 14 Spanish centers between January 2000 and January 2019 were included. Median age was 44 (31-67) years. After a median follow-up of 58 months, estimated 5-year overall survival (OS) and progression-free survival (PFS) were both 35%. Estimated 100-day and 1-year non-relapse mortality (NRM) were 20% and 34%, respectively. The type of conditioning regimen (3-year OS of 52% vs. 20%, respectively, for reduced-intensity vs. myeloablative conditioning) and development of chronic graft versus host disease (cGVHD) (3-year OS of 75% vs. 40%) were the only factors significantly associated with OS. The only variable with an independent association with OS was cGVHD (HR, 3.4; 95% CI, 1.2-9.6).

Conclusions: Our results indicate that alloSCT continues to be a potentially curative option for patients with tFL.

Keywords: allogeneic stem cell transplantation; follicular lymphoma; non-Hodgkin lymphoma; transformed lymphoma.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
(a) Overall survival (OS) and (b) progression-free survival (PFS) in the global series.
Figure 1
Figure 1
(a) Overall survival (OS) and (b) progression-free survival (PFS) in the global series.
Figure 2
Figure 2
(a) Overall survival (OS) for reduced-intensity conditioning (RIC) and myeloablative conditioning (MAC) regimens. (b) OS according to chronic graft-vs-host disease (cGVHD). (c) OS according to lymphoma status pre-alloSCT, complete response (CR) or other response.
Figure 2
Figure 2
(a) Overall survival (OS) for reduced-intensity conditioning (RIC) and myeloablative conditioning (MAC) regimens. (b) OS according to chronic graft-vs-host disease (cGVHD). (c) OS according to lymphoma status pre-alloSCT, complete response (CR) or other response.
Figure 3
Figure 3
(a) Progression free-survival (PFS) for reduced-intensity conditioning (RIC) and myeloablative conditioning (MAC) regimens. (b) PFS according to chronic graft-vs-host disease (cGVHD). (c) PFS according to lymphoma status pre-alloSCT, complete response (CR) or other response.
Figure 3
Figure 3
(a) Progression free-survival (PFS) for reduced-intensity conditioning (RIC) and myeloablative conditioning (MAC) regimens. (b) PFS according to chronic graft-vs-host disease (cGVHD). (c) PFS according to lymphoma status pre-alloSCT, complete response (CR) or other response.
Figure 4
Figure 4
Non-relapse mortality (NRM) in global series.
Figure 5
Figure 5
(a) Non-relapse mortality (NRM) for RIC and MAC regimens. (b) NRM for sibling vs. unrelated vs. haploidentical transplanta-tion.

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