2-deoxy-2[F-18] fluoro-D-glucose positron emission tomography Deauville scale and core-needle biopsy to determine successful management after six doxorubicin, bleomycin, vinblastine and dacarbazine cycles in advanced-stage Hodgkin lymphoma.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
06 2020
Historique:
received: 27 11 2019
revised: 14 03 2020
accepted: 18 03 2020
pubmed: 26 4 2020
medline: 11 11 2020
entrez: 26 4 2020
Statut: ppublish

Résumé

The clinical impact of the positivity of the Deauville scale (DS) of positron emission tomography (PET) performed at the end of doxorubicin, bleomycin, vinblastine and dacarbazine (ABVD) in patients with advanced Hodgkin lymphoma (HL), in terms of providing rationale to shift poor responders onto a more intensive regimen, remain to be validated by histopathology. This prospective trial involved patients with stage IIB/IV HL who after six ABVD cycles underwent PET (PET6) and core-needle cutting biopsy (CNCB) of 2-deoxy-2[F-18] fluoro-d-glucose (FDG)-avid lymph nodes. Patients received high-dose chemotherapy/autologous haematopoietic stem cell rescue (HDCT/AHSCR) if CNCB was positive for HL, alternatively, if CNCB or PET was negative, received observation or consolidation radiotherapy (cRT) on residual nodal masses, as initially planned. The end-point was 5-year progression-free survival (PFS). In all, 43 of the 169 (25%) evaluable patients were PET6 positive (DS 4, 32; DS 5, 11). Among them, histology showed malignancy (HL) in 100% of DS 5 scores and in 12.5% of DS 4 scores. Fifteen patients with positive biopsy received HDCT/AHSCR, whereas 28 patients with negative biopsy, as well as 126 patients with negative PET6, continued the original plan (cRT, 78 patients; observation, 76 patients). The 5-year PFS in the negative PET6 group, negative biopsy group and positive biopsy group was 95.4%, 100% and 52.5%, respectively. DS positivity of end-of-ABVD PET in advanced HL carried a certain number of CNCB-proven non-malignant FDG-uptakes. The DS 4 scores which were found to have negative histology appeared to benefit from continuing the original non-intensive therapeutic plane as indicated by the successful outcome in more than 95% of them by obtaining similar 5-year PFS to the PET6-negative group. By contrast, the DS 5 score had consistently positive histology and was associated with unsuccessful conventional therapy, promptly requiring treatment intensification or innovative therapeutic approaches.

Sections du résumé

BACKGROUND
The clinical impact of the positivity of the Deauville scale (DS) of positron emission tomography (PET) performed at the end of doxorubicin, bleomycin, vinblastine and dacarbazine (ABVD) in patients with advanced Hodgkin lymphoma (HL), in terms of providing rationale to shift poor responders onto a more intensive regimen, remain to be validated by histopathology.
PATIENTS AND METHODS
This prospective trial involved patients with stage IIB/IV HL who after six ABVD cycles underwent PET (PET6) and core-needle cutting biopsy (CNCB) of 2-deoxy-2[F-18] fluoro-d-glucose (FDG)-avid lymph nodes. Patients received high-dose chemotherapy/autologous haematopoietic stem cell rescue (HDCT/AHSCR) if CNCB was positive for HL, alternatively, if CNCB or PET was negative, received observation or consolidation radiotherapy (cRT) on residual nodal masses, as initially planned. The end-point was 5-year progression-free survival (PFS).
RESULTS
In all, 43 of the 169 (25%) evaluable patients were PET6 positive (DS 4, 32; DS 5, 11). Among them, histology showed malignancy (HL) in 100% of DS 5 scores and in 12.5% of DS 4 scores. Fifteen patients with positive biopsy received HDCT/AHSCR, whereas 28 patients with negative biopsy, as well as 126 patients with negative PET6, continued the original plan (cRT, 78 patients; observation, 76 patients). The 5-year PFS in the negative PET6 group, negative biopsy group and positive biopsy group was 95.4%, 100% and 52.5%, respectively.
CONCLUSION
DS positivity of end-of-ABVD PET in advanced HL carried a certain number of CNCB-proven non-malignant FDG-uptakes. The DS 4 scores which were found to have negative histology appeared to benefit from continuing the original non-intensive therapeutic plane as indicated by the successful outcome in more than 95% of them by obtaining similar 5-year PFS to the PET6-negative group. By contrast, the DS 5 score had consistently positive histology and was associated with unsuccessful conventional therapy, promptly requiring treatment intensification or innovative therapeutic approaches.

Identifiants

pubmed: 32334339
pii: S0959-8049(20)30149-0
doi: 10.1016/j.ejca.2020.03.008
pii:
doi:

Substances chimiques

Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D
Bleomycin 11056-06-7
Vinblastine 5V9KLZ54CY
Dacarbazine 7GR28W0FJI
Doxorubicin 80168379AG
Glucose IY9XDZ35W2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

85-97

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement Authors have no relevant financial conflict of interest to declare.

Auteurs

M Picardi (M)

Department of Clinical Medicine and Surgery, Federico II University Medical School, Naples, Italy.

R Fonti (R)

Institute of Biostructures and Bioimages, National Research Council, Naples, Italy.

R Della Pepa (R)

Department of Clinical Medicine and Surgery, Federico II University Medical School, Naples, Italy. Electronic address: roberta.dellapepa@unina.it.

C Giordano (C)

Department of Clinical Medicine and Surgery, Federico II University Medical School, Naples, Italy.

N Pugliese (N)

Department of Clinical Medicine and Surgery, Federico II University Medical School, Naples, Italy.

E Nicolai (E)

IRCCS SDN, Naples, Italy.

M Salvatore (M)

IRCCS SDN, Naples, Italy.

C Mainolfi (C)

Institute of Biostructures and Bioimages, National Research Council, Naples, Italy.

P Venetucci (P)

Department of Advanced Biomedical Sciences, Federico II University Medical School, Naples, Italy.

M G Rascato (MG)

Department of Clinical Medicine and Surgery, Federico II University Medical School, Naples, Italy.

I Cappuccio (I)

Department of Clinical Medicine and Surgery, Federico II University Medical School, Naples, Italy.

M Mascolo (M)

Department of Advanced Biomedical Sciences, Federico II University Medical School, Naples, Italy.

E Vigliar (E)

Department of Public Health, Federico II University Medical School Naples, Italy.

G Troncone (G)

Department of Public Health, Federico II University Medical School Naples, Italy.

S Del Vecchio (S)

Department of Advanced Biomedical Sciences, Federico II University Medical School, Naples, Italy.

F Pane (F)

Department of Clinical Medicine and Surgery, Federico II University Medical School, Naples, Italy.

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