CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2016; 37(02): 106-111
DOI: 10.4103/0971-5851.180142
ORIGINAL ARTICLE

ABVE-PC and modified BEACOPP regimen in Indian children with Hodgkin lymphoma: Feasibility and efficacy

Somasundaram Jayabose
Department of Pediatric Hematology and Oncology, Meenakshi Mission Hospital and Research Centre, Madurai, Tamil Nadu, India
,
Kasi Viswanathan
Department of Pediatric Hematology and Oncology, Meenakshi Mission Hospital and Research Centre, Madurai, Tamil Nadu, India
,
Vignesh Kumar
Department of Pediatric Hematology and Oncology, Meenakshi Mission Hospital and Research Centre, Madurai, Tamil Nadu, India
,
Annapoorani Annamalai
Department of Pediatric Hematology and Oncology, Meenakshi Mission Hospital and Research Centre, Madurai, Tamil Nadu, India
,
Arathi Srinivasan
Department of Pediatric Oncology, Kanchi Kamakoti Childs Trust Hospital, Chennai, Tamil Nadu, India
,
Julius Xavier Scott
Department of Pediatric Oncology, Kanchi Kamakoti Childs Trust Hospital, Chennai, Tamil Nadu, India
,
Krishnakumar Rathnam
Department of Pediatric Hematology and Oncology, Meenakshi Mission Hospital and Research Centre, Madurai, Tamil Nadu, India
› Author Affiliations
Financial support and sponsorship Nil.

Abstract

Aims: To study the toxicity of ABVE-PC (doxorubicin, bleomycin, vincristine, etoposide, prednisone and cyclophosphamide) and modified-BEACOPP (bleomycin, etoposide, doxorubicin, cyclophosphamide,vincristine, procarbazine, prednisone) in intermediate-risk and high-risk Hodgkin lymphoma patients. Methods: High-risk patients received 4 cycles of modified-BEACOPP (m-BEACOPP) plus 4 cycles of ABVD. Intermediate-risk patients received 4 cycles of ABVE-PC plus 2 cycles of ABVD. Results: From 2010 to 2014, 17 patients received 66 cycles of m-BEACOPP and 9 patients received 40 cycles of ABVE-PC. In the m-BEACOPP and ABVE-PC courses, respectively, significant thrombocytopenia (<50,000/mm3) occurred in 10.6% vs 0% of courses; anemia (Hb. <8 gm/dl) in 27.3% vs 15%; neutropenia (ANC<500/mm3) in 46.9% vs 32.5%; and febrile neutropenia in 33.3% vs. 22.5%. Only episode of documented infection (hepatic abscess) occurred in ABVE-PC. There were no episodes of sepsis, typhlitis or pneumonia in either group. All 26 patients are in remission with a median follow-up of 35 months (range, 17-61); and there have been no relapses. Two of 26 (7.7%) patients failed to achieve rapid early response after 2 cycles and complete remission after 4 cycles of chemotherapy; both achieved remission with more intensive regimens followed by radiation. The remaining 24 patients did not receive radiation therapy. Conclusions: Both m-BEACOPP and ABVE-PC regimens have acceptable toxicity; and thus can be used in most centres with optimum supportive care facilities. They offer promising response rate and relapse free survival without the need for radiation therapy in most patients; and thus may be considered for children with high-risk and intermediate-risk Hodgkin lymphoma.



Publication History

Article published online:
12 July 2021

© 2016. Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/.)

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