Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 May;59(5):604-614.
doi: 10.1038/s41409-024-02226-1. Epub 2024 Feb 8.

Hematopoietic stem cell transplantation for pediatric patients with non-anaplastic peripheral T-cell lymphoma. An EBMT pediatric diseases working party study

Affiliations

Hematopoietic stem cell transplantation for pediatric patients with non-anaplastic peripheral T-cell lymphoma. An EBMT pediatric diseases working party study

Olga Moser et al. Bone Marrow Transplant. 2024 May.

Abstract

Peripheral T-cell lymphomas (PTCL) other than anaplastic large-cell lymphoma are rare in children, and the role of hematopoietic stem cell transplantation (HSCT) has not been clarified yet. In a retrospective analysis of registry-data of the European Society for Blood and Marrow Transplantation we analyzed 55 patients aged < 18 years who received allogeneic (N = 46) or autologous (N = 9) HSCT for PTCL. Median age at HSCT was 13.9 years; 33 patients (60%) were in first remission, and 6 (19%) in progression at HSCT. Conditioning was myeloablative in 87% of the allogeneic HSCTs and in 27 (58.7%) based on total body irradiation. After allogeneic HSCT the 5-year overall- and progression-free survival was 58.9% (95% CI 42.7-71.9) and 52.6% (95% CI 36.8-66.1), respectively. 5-year relapse incidence was 27.6% (95% CI 15.1-41.6), the non-relapse mortality rate was 19.8% (95% CI 9.7-32.6). Five of the six patients with progression at HSCT died. Seven of nine patients after autologous HSCT were alive and disease-free at last follow-up. Our data suggest a role of allogeneic HSCT in consolidation-treatment of patients with high-risk disease, who reach at least partial remission after primary- or relapse-therapy, whereas patients with therapy-refractory or progressive disease prior to transplantation do not profit from HSCT.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Study population chart. Numbers of patients screened from the EBMT-database for inclusion in the present study.
Fig. 2
Fig. 2. Study population chart Numbers of patients screened from the EBMT-database for inclusion in the present study.
Outcome estimates after allogeneic HSCT: a Kaplan-Meier estimates of overall survival (OS). The 2-year OS was 66.8% (95% CI 51.1–78.5), the 5-year OS was 58.9% (95% CI 42.7–71.9), respectively. b Probability of progression-free survival (PFS): The 2-year PFS was 55.3% (95% CI 39.6-68.5), the 5-year PFS was 52.6% (95% CI 36.8-66.1), respectively. c Cumulative relapse incidence (RI): 2-year cumulative RI was 24.9% (95% CI 13.2–38.4), 5-year cumulative RI was 27.6% (95% CI 15.1–41.6), respectively. d Estimate of non-relapse mortality (NRM): the 2-year and 5-year NRM was 19.8% (95% CI 9.7–32.6).

Similar articles

Cited by

References

    1. Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, et al. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. IARC, Lyon. (2017).
    1. Kobayashi R, Yamato K, Tanaka F, Takashima Y, Inada H, Kikuchi A, et al. Retrospective analysis of nonanaplastic peripheral T-cell lymphoma in pediatric patients in Japan. Pediatr Blood Cancer. 2010;54:212–5. doi: 10.1002/pbc.22329. - DOI - PubMed
    1. Kontny U, Oschlies I, Woessmann W, Burkhardt B, Lisfeld J, Salzburg J, et al. Non-anaplastic peripheral T-cell lymphoma in children and adolescents—a retrospective analysis of the NHL-BFM study group. Br J Haematol. 2015;168:835–44. doi: 10.1111/bjh.13216. - DOI - PubMed
    1. Windsor R, Stilles C, Webb D. Peripheral T-cell lymphomas in childhood: population-based experience in the United Kingdom over 20 years. Pediatr Blood Cancer. 2008;50:784–7. doi: 10.1002/pbc.21293. - DOI - PubMed
    1. Flower A, Xavier AC, Cairo MS. Mature (non-anaplastic, non-cutaneous) T-/NK-cell lymphomas in children, adolescents and young adults: state of the science. Br J Haematol. 2019;185:418–35. doi: 10.1111/bjh.15767. - DOI - PubMed