Long-term results of PET-guided radiation in patients with advanced-stage diffuse large B-cell lymphoma treated with R-CHOP.


Journal

Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509

Informations de publication

Date de publication:
18 02 2021
Historique:
received: 18 03 2020
accepted: 13 08 2020
pubmed: 2 9 2020
medline: 3 7 2021
entrez: 2 9 2020
Statut: ppublish

Résumé

Consolidative radiation therapy (RT) for advanced-stage diffuse large B-cell lymphoma (DLBCL) remains controversial, with routine practice continuing to include RT in patients with initial bulky disease or residual masses. Positron emission tomography (PET)-computed tomography is a sensitive modality for detecting the presence of residual disease at the end of treatment (EOT). A PET-guided approach to selectively administering RT has been the policy in British Columbia since 2005. Patients with advanced-stage DLBCL diagnosed from 1 January 2005 to 1 March 2017 and treated with at least 6 cycles of R-CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone plus rituximab), who underwent EOT PET, were included in this analysis. Those with complete metabolic response (PET-negative [PET-NEG]) were observed; those with PET-positive (PET-POS) scans were offered consolidative RT, when feasible. Of the patient records reviewed, 723 were identified, with median follow-up of 4.3 years: 517 (72%) were PET-NEG; 206 (28%) were PET-POS. Time to progression (TTP) and overall survival (OS) at 3 years were 83% vs 56% and 87% vs 64%, in patients with PET-NEG and PET-POS scans, respectively. PET-POS patients with nonprogressing disease treated with consolidative RT (109 and 206; 53%) had outcomes approaching those of PET-NEG patients, with 3-year estimates of 76% and 80% for TTP and OS. PET-NEG patients who had bulky disease (≥10 cm) at diagnosis had outcomes indistinguishable from those without bulk, despite the omission of RT. These data suggest that patients with advanced-stage DLBCL who are PET-NEG at EOT and receive no RT have excellent outcomes. 18F-fluorodeoxyglucose-PET can reliably guide selective administration of consolidative RT, even in patients with initially bulky disease.

Identifiants

pubmed: 32871586
pii: S0006-4971(21)00314-1
doi: 10.1182/blood.2020005846
doi:

Substances chimiques

Fluorine Radioisotopes 0
Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D
Rituximab 4F4X42SYQ6
Vincristine 5J49Q6B70F
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
Fluorine-18 GZ5I74KB8G
Prednisone VB0R961HZT

Types de publication

Comparative Study Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

929-938

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 by The American Society of Hematology.

Auteurs

Ciara L Freeman (CL)

Centre for Lymphoid Cancer, BC Cancer, Vancouver, BC, Canada.
Division of Medical Oncology, University of British Columbia, Vancouver, BC, Canada.

Kerry J Savage (KJ)

Centre for Lymphoid Cancer, BC Cancer, Vancouver, BC, Canada.
Division of Medical Oncology, University of British Columbia, Vancouver, BC, Canada.

Diego R Villa (DR)

Centre for Lymphoid Cancer, BC Cancer, Vancouver, BC, Canada.
Division of Medical Oncology, University of British Columbia, Vancouver, BC, Canada.

David W Scott (DW)

Centre for Lymphoid Cancer, BC Cancer, Vancouver, BC, Canada.
Division of Medical Oncology, University of British Columbia, Vancouver, BC, Canada.

Line Srour (L)

Division of Hematology and Medical Oncology, Department of Medicine, CISSS Montérégie Centre/Hôpital Charles-Lemoyne, Université Sherbrooke, QC, Canada; and.

Alina S Gerrie (AS)

Centre for Lymphoid Cancer, BC Cancer, Vancouver, BC, Canada.
Division of Medical Oncology, University of British Columbia, Vancouver, BC, Canada.

Maura J Brown (MJ)

Department of Diagnostic Imaging.

Graham W Slack (GW)

Department of Pathology and Laboratory Medicine.

Pedro Farinha (P)

Department of Pathology and Laboratory Medicine.

Brian Skinnider (B)

Department of Pathology and Laboratory Medicine.

James Morris (J)

Division of Radiation Oncology, and.

François Bénard (F)

Department of Functional Imaging, BC Cancer, Vancouver, BC, Canada.

Christina Aquino-Parsons (C)

Division of Radiation Oncology, and.

Andrea Lo (A)

Division of Radiation Oncology, and.

Tom Pickles (T)

Division of Radiation Oncology, and.

Don C Wilson (DC)

Department of Functional Imaging, BC Cancer, Vancouver, BC, Canada.

Petter Tonseth (P)

Department of Functional Imaging, BC Cancer, Vancouver, BC, Canada.

Joseph M Connors (JM)

Centre for Lymphoid Cancer, BC Cancer, Vancouver, BC, Canada.
Division of Medical Oncology, University of British Columbia, Vancouver, BC, Canada.

Laurie H Sehn (LH)

Centre for Lymphoid Cancer, BC Cancer, Vancouver, BC, Canada.
Division of Medical Oncology, University of British Columbia, Vancouver, BC, Canada.

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