Real-world results of first-line ABVD in patients with classic Hodgkin's lymphoma at a neoplastic disease institute in Lima, Peru.

Objective: To evaluate the clinical characteristics and outcomes of first-line ABVD (doxorubicin, bleomycin, vinblastine, dacarbazine) in patients with classical Hodgkin lymphoma treated at a neoplastic disease institute in Lima, Peru. Methods: Retrospective study of previously untreated classical H...

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Published in:Revista Medica Herediana Vol. 36; no. 4; pp. 332 - 345
Main Authors: Salinas Agramonte, Luis, Valencia Laurel, Grethel, Alcarraz, Cindy, Mantilla, Raúl, Quintana, Shirley, Vásquez, Jule, Rioja, Patricia, Bendezú, Elmer, Motta Guerrero, Rodrigo, Vidaurre, Tatiana
Format: research tables/charts Journal Article
Published: Universidad Peruana Cayetano Heredia Oct-Dec2025
Online Access:View this record in EBSCOhost
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      dt: Oct-Dec2025
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      pub: Universidad Peruana Cayetano Heredia
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        10.20453/rmh.v36i4.6535
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        atl: Real-world results of first-line ABVD in patients with classic Hodgkin's lymphoma at a neoplastic disease institute in Lima, Peru.
      aug:
        au:
          Salinas Agramonte, Luis
          Valencia Laurel, Grethel
          Alcarraz, Cindy
          Mantilla, Raúl
          Quintana, Shirley
          Vásquez, Jule
          Rioja, Patricia
          Bendezú, Elmer
          Motta Guerrero, Rodrigo
          Vidaurre, Tatiana
        affil: Departamento de Medicina Oncológica. Instituto Nacional de Enfermedades Neoplásicas. Lima, Perú
      sug:
        subj:
          Hodgkin's Disease Drug Therapy
          Doxorubicin Therapeutic Use
          Bleomycins Therapeutic Use
          Vinblastine Therapeutic Use
          Dacarbazine Therapeutic Use
          Treatment Outcomes
          Human
          Peru
          Male
          Female
          Adult
          Middle Age
          Retrospective Design
          Record Review
          Nonexperimental Studies
          Descriptive Statistics
          Cox Proportional Hazards Model
          Prospective Studies
          Confidence Intervals
          Data Analysis Software
          Progression-Free Survival
          Overall Survival
          Neoplasm Staging
          Neutropenia
          Nausea
          Drug Combinations
          Adult: 19-44 years
          Middle Aged: 45-64 years
          Male
          Female
      ab:
        Objective: To evaluate the clinical characteristics and outcomes of first-line ABVD (doxorubicin, bleomycin, vinblastine, dacarbazine) in patients with classical Hodgkin lymphoma treated at a neoplastic disease institute in Lima, Peru. Methods: Retrospective study of previously untreated classical Hodgkin lymphoma diagnosed between 2014 and 2018. All received ABVD days 1 and 15 every 28 days. We described clinical features, objective response rate (ORR), overall survival (OS), and adverse events (AEs) per CTCAE v5.0, and explored associations between clinical variables and response using the chi-square test. Results: A total of 157 patients were included, with a median age of 31.5 years (interquartile range [IQR]: 22-49.25), of whom 56.7% were male. The most common histological type was nodular sclerosis (64.3%). Bulky disease was present in 17.8%, mediastinal mass in 45.2%, and B symptoms in 76.4%. Disease stages were distributed as follows: stage I (5.1%), stage II (36.9%), stage III (34.4%), and stage IV (22.9%). The complete response (CR) rate was 97.1%. Over the 36 months, overall survival (OS) was 83.1%. Regarding toxicity, grade 3-4 neutropenia occurred in 31.8%, while the most frequent non-hematological toxicity was nausea (24.8%). Conclusions: In this cohort, first-line ABVD showed effectiveness with a toxicity profile comparable to prior reports, supporting its use in resource-limited settings. Optimizing supportive care and incorporating PET/ CT may help refine treatment selection and follow-up.
        Objetivo: Evaluar las características clínicas y los resultados del tratamiento de primera línea con ABVD (doxorrubicina, bleomicina, vinblastina y dacarbazina) en pacientes con linfoma de Hodgkin clásico atendidos en un instituto de enfermedades neoplásicas en Lima, Perú. Material y métodos: Estudio retrospectivo de pacientes con linfoma de Hodgkin clásico no tratados previamente, diagnosticados entre 2014 y 2018. Todos recibieron ABVD días 1 y 15 cada 28 días. Se describieron características clínicas, tasa de respuesta objetiva (TRO), supervivencia global (SG) y eventos adversos (EA) según CTCAE v5.0. Se exploraron asociaciones entre variables clínicas y respuesta mediante prueba de chi cuadrado. Resultados: Se incluyeron 157 pacientes con una mediana de edad de 31,5 años (rango intercuartílico [RIC]: 22-49,25), de los cuales el 56,7% eran varones. El tipo histológico más frecuente fue la esclerosis nodular (64,3%). El 17,8% presentaron enfermedad bulky, el 45,2% masa mediastinal y el 76,4% síntomas B. La distribución por estadios fue: estadio I (5,1%), estadio II (36,9%), estadio III (34,4%) y estadio IV (22,9%). La tasa de respuesta completa (RC) alcanzó el 97,1%. A los 36 meses, la supervivencia global (SG) fue del 83,1%. En cuanto a la toxicidad, la neutropenia de grado 3-4 se observó en el 31,8%, mientras que la toxicidad no hematológica más frecuente fueron las náuseas (24,8%). Conclusiones: En esta cohorte, el ABVD de primera línea mostró efectividad y un perfil de toxicidad seguro. La optimización del soporte y el empleo de PET/CT podrían contribuir a racionalizar mejor el tratamiento.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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