Hitting a Moving Target: Successful Management of Diffuse Large B-cell Lymphoma Involving the Mesentery With Volumetric Image-guided Intensity Modulated Radiation Therapy.


Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
01 2019
Historique:
received: 28 06 2018
revised: 24 08 2018
accepted: 04 09 2018
pubmed: 27 10 2018
medline: 23 2 2020
entrez: 27 10 2018
Statut: ppublish

Résumé

We report successful treatment of mesenteric diffuse large B-cell lymphoma (DLBCL) using localized involved site radiation therapy (ISRT), intensity modulated radiation therapy (IMRT), and daily computed tomography (CT)-image guidance. Patients with mesenteric DLBCL treated with RT between 2011 and 2017 were reviewed. Clinical and treatment characteristics were analyzed for an association with local control, progression-free survival (PFS), and overall survival. Twenty-three patients were eligible. At diagnosis, the median age was 52 years (range, 38-76 years), and 57% (n = 13) had stage I/II DLBCL. All patients received frontline chemotherapy (ChT) (R-CHOP [rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone], n = 19; dose-adjusted R-EPOCH [rituximab, etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin], n = 4) with median 6 cycles. Prior to RT, salvage ChT for refractory DLBCL was given to 43% (n = 10) and autologous stem cell transplantation was administered in 13% (n = 3). At the time of RT, positron emission tomography-CT revealed 5-point scale of 1 to 3 (48%; n = 11), 4 (9%; n = 2), and 5 (44%; n = 10). All patients received IMRT, daily CT imaging, and ISRT. The median RT dose was 40 Gy (range, 16.2-49.4 Gy). Relapse or progression occurred in 22% (n = 5). At a median follow-up of 37 months, the 3-year local control, PFS, and overall survival rates were 80%, 75%, and 96%, respectively. Among patients treated with RT after complete metabolic response to frontline ChT (n = 8), the 3-year PFS was 100%, compared with 61% for patients with a history of chemorefractory DLBCL (n = 15; P = .055). Four of the 5 relapses occurred in patients with 5-point scale of 5 prior to RT (P = .127). Mesenteric involvement of DLBCL can be successfully targeted with localized ISRT fields using IMRT and daily CT-image guidance.

Identifiants

pubmed: 30360985
pii: S2152-2650(18)30687-6
doi: 10.1016/j.clml.2018.09.002
pmc: PMC6371800
mid: NIHMS1506228
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e51-e61

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

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Auteurs

Alison K Yoder (AK)

Baylor College of Medicine, Houston, TX.

Jillian R Gunther (JR)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Sarah A Milgrom (SA)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Dragan Mirkovic (D)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Loretta Nastoupil (L)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.

Sattva Neelapu (S)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.

Michelle Fanale (M)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.

Nathan Fowler (N)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.

Jason Westin (J)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.

Hun Ju Lee (HJ)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.

M Alma Rodriguez (MA)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.

Swaminathan P Iyer (SP)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.

Luis Fayad (L)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.

Yago L Nieto (YL)

Department of Stem Cell Transplantation, The University of Texas MD Anderson Cancer Center, Houston, TX.

Chitra Hosing (C)

Department of Stem Cell Transplantation, The University of Texas MD Anderson Cancer Center, Houston, TX.

Sairah Ahmed (S)

Department of Stem Cell Transplantation, The University of Texas MD Anderson Cancer Center, Houston, TX.

L Jeffrey Medeiros (LJ)

Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Joseph D Khoury (JD)

Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Naveen Garg (N)

Department of Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Behrang Amini (B)

Department of Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Bouthaina S Dabaja (BS)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Chelsea C Pinnix (CC)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX. Electronic address: ccpinnix@mdanderson.org.

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