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Outcomes of CHOP versus CHOEP/EPOCH in aggressive adult T-cell leukemia/lymphoma: an international cohort analysis

Bryan Valcarcel, Jule F. Vasquez, Daniel Enriquez‐Vera, Brady E. Beltran and 18 more

Haematologica | Sep 10, 2026

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CHOEP/EPOCH may be associated with improved survival in lymphomatous ATL, while results in acute ATL were inconclusive, and the need for prospective interventional studies to validate the subtype-specific benefits is supported.

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Aggressive adult T-cell leukemia/lymphoma (ATL) subtypes (i.e., acute and lymphomatous) are rare diseases, and the conventional management with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) has historically yielded poor outcomes. The benefit of etoposide-containing regimens (CHOEP/EPOCH) in the first-line setting is inconclusive. We compared the effectiveness of CHOEP/EPOCH versus CHOP in aggressive ATL. We conducted an international, multicenter retrospective cohort study among newly diagnosed patients with ATL during 2000-2023 across five Latin American countries and the United States. Study endpoints included overall response rate (ORR) and overall survival (OS). Propensity score weighting was used to balance the treatment groups, and findings are reported for each ATL subtype. Among 328 patients, 108 had acute ATL and 220 had lymphomatous ATL. In weighted analyses, CHOEP/EPOCH was not statistically associated with a higher ORR compared to CHOP in lymphomatous ATL (66% vs. 58%; Odds ratio [OR]=2.08, 95% confidence interval [CI]=0.76-5.75) or acute ATL (42% vs. 58%; OR=0.68, 95% CI=0.06-7.84). With a median follow-up of 34 months (interquartile range [IQR] 15-73) in lymphomatous ATL, CHOEP/EPOCH was associated with a higher 3-year OS (34% vs. 12%; HR=0.55, 95% CI=0.35-0.87). However, with a median follow-up of 63 months (IQR 16-110) in acute ATL, CHOEP/EPOCH was not associated with improved 3-year OS (8% vs. 11%; HR=0.95, 95% CI=0.51-1.77). In conclusion, CHOEP/EPOCH may be associated with improved survival in lymphomatous ATL, while results in acute ATL were inconclusive. These findings support the need for prospective interventional studies to validate the subtype-specific benefits.

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Bryan Valcarcel

first | The University of Texas MD Anderson Cancer Center | ORCID 0000-0003-3853-2603

Jule F. Vasquez

middle | Instituto Nacional de Enfermedades Neoplásicas

Daniel Enriquez‐Vera

middle | Universidad Privada San Juan Bautista

Brady E. Beltran

middle | Universidad San Ignacio de Loyola

Denisse Castro

middle | Universidad San Ignacio de Loyola | ORCID 0000-0002-5108-9493

Thanya Runciman

middle | Hospital Base Guillermo Almenara Irigoyen | ORCID 0000-0003-3915-4886

Henry Idrobo

middle | Technological University of Pereira | ORCID 0000-0002-7686-5874

Elizabeth Arrieta

middle | Fundación Valle del Lili | ORCID 0000-0002-3714-4476

Oriana Arias

middle | Fundación Valle del Lili

Macarena Roa

middle | Hospital del Salvador | ORCID 0000-0002-2351-8158

Camila Peña

middle | Hospital del Salvador | ORCID 0000-0002-8076-2077

Lorena Fiad

middle | Hospital Italiano La Plata | ORCID 0000-0003-4816-7523

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BibTeX

@article{Valcarcel2026Outcomes,
  title = {Outcomes of CHOP versus CHOEP/EPOCH in aggressive adult T-cell leukemia/lymphoma: an international cohort analysis},
  author = {Bryan Valcarcel and Jule F. Vasquez and Daniel Enriquez‐Vera and Brady E. Beltran and Denisse Castro and Thanya Runciman and Henry Idrobo and Elizabeth Arrieta and Oriana Arias and Macarena Roa and Camila Peña and Lorena Fiad and Juan C. Ramos and Jose Sandoval-Sus and Abat Khan and Alejandro Sica and Britney N. Bell and Yumeng Zhang and Veronica Leautaud and Eliana C M CM Miranda and Carlos Chiattone and Luis Malpica},
  journal = {Haematologica},
  year = {2026},
  doi = {10.3324/haematol.2026.300969},
  url = {https://doi.org/10.3324/haematol.2026.300969}
}

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