Early chemotherapy de-escalation strategy in patients with advanced-stage Hodgkin lymphoma with negative positron emission tomography scan after 2 escalated BEACOPP cycles.


Journal

Polish archives of internal medicine
ISSN: 1897-9483
Titre abrégé: Pol Arch Intern Med
Pays: Poland
ID NLM: 101700960

Informations de publication

Date de publication:
30 04 2019
Historique:
pubmed: 5 4 2019
medline: 5 6 2020
entrez: 5 4 2019
Statut: ppublish

Résumé

INTRODUCTION Escalated BEACOPP (escBEACOPP: bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, prednisone) significantly improves overall response rates (ORRs) and prolongs progression‑free survival (PFS) in patients with advanced‑stage Hodgkin lymphoma (HL). However, 6 to 8 cycles of escBEACOPP are associated with increased acute toxicity and late complications. OBJECTIVES We aimed to determine the role of early positron emission tomography-computed tomography (PET‑CT) response assessment in a de‑escalation strategy. PATIENTS AND METHODS We retrospectively analyzed 188 consecutive patients with advanced‑stage HL treated at diagnosis. Patients received 2 cycles of escBEACOPP followed by an early PET‑CT response assessment performed after 2 cycles of chemotherapy (PET2). Patients with an active disease continued therapy with escBEACOPP, while those with negative PET2 were de‑escalated to ABVD (doxorubicin, bleomycin, vinblastine, dacarbazine). Radiotherapy was allowed in patients with stage IIBX. RESULTS PET2 allowed for de‑escalation of therapy in 141 patients (75%). Their ORR was 92.2%, with a complete remission (CR) rate of 91.5%; 10‑year PFS and overall survival (OS) were 87.2% and 95%, respectively. In the whole cohort, ORR was 87.8% (CR, 85.6%), while the 10‑year PFS and OS were 79.3% and 89.4%, respectively. Hematological and thromboembolic complications were significantly more frequent in patients treated with 6 escBEACOPP cycles, including febrile neutropenia (25 patients, [53.2%] vs 7 [5%]), serious anemia (35 [74.5%] vs 11 [7.8%]), or thrombocytopenia (16 [34%] vs 7 [5%]) (P <0.001 for all comparisons with de‑escalation strategy) as well as pulmonary embolism (3 [6.4%] vs 0) (P = 0.02). CONCLUSIONS The early de‑escalation strategy allows for effective treatment of advanced HL, with a comparable efficacy to that of 6 to 8 cycles of escBEACOPP, but with significantly reduced toxicity.

Identifiants

pubmed: 30945698
doi: 10.20452/pamw.14786
doi:

Substances chimiques

Bleomycin 11056-06-7
Procarbazine 35S93Y190K
Vincristine 5J49Q6B70F
Etoposide 6PLQ3CP4P3
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
Prednisone VB0R961HZT

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

259-266

Auteurs

Monika Długosz-Danecka (M)

Department of Hematology, Jagiellonian University Medical College, Kraków, Poland

Sebastian Szmit (S)

Department of Pulmonary Circulation, Thromboembolic Diseases and Cardiology, Centre of Postgraduate Medical Education, European Health Centre, Otwock, Poland

Anna Kocurek (A)

Department of Medical Education, Jagiellonian University, Kraków, Poland

Paweł Koźlik (P)

Department of Allergy and Immunology, Jagiellonian University Medical College, Kraków, Poland

Agnieszka Giza (A)

Department of Hematology, Jagiellonian University Medical College, Kraków, Poland

Dagmara Zimowska-Curyło (D)

Department of Hematology, Jagiellonian University Medical College, Kraków, Poland

Bogdan Małkowski (B)

Department of Positron Emission Tomography and Molecular Imaging, Nicolaus Copernicus University, Collegium Medicum, Bydgoszcz, Poland

Anna Sowa-Staszczak (A)

Department of Endocrinology, Jagiellonian University Medical College, Kraków, Poland

Jarosław Kużdżał (J)

Department of Thoracic and Surgical Oncology, Jagiellonian University Medical College, John Paul II Hospital, Kraków, Poland

Wojciech Jurczak (W)

Department of Hematology, Jagiellonian University Medical College, Kraków, Poland

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Classifications MeSH