Early Stage Extranodal Follicular Lymphoma: Characteristics, Management, and Outcomes.


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:
06 2019
Historique:
received: 21 10 2018
revised: 20 01 2019
accepted: 15 02 2019
pubmed: 3 4 2019
medline: 28 7 2020
entrez: 3 4 2019
Statut: ppublish

Résumé

Extranodal follicular lymphoma (E-FL) is a rare entity that has distinct characteristics and outcomes compared with nodal follicular lymphoma. This cohort comprised 37 patients with stages I/II E-FL, diagnosed from 2003 to 2013. Outcomes included progression-free survival (PFS), and overall survival (OS). Survival outcomes were calculated using Kaplan-Meier methods. Median age was 60 years (range, 37-84 years). Disease was stage I in 29 (78.4%). The Follicular Lymphoma International Prognostic Index score was 0 to 1 in 31 (83.8%), 2 in 2 (5.4%), 3 in 1 (2.7%), and missing in 3 (8.1%). Sites of involvement included the gastrointestinal (GI) tract in 22 (59.5%), and non-GI sites in 15 (40.5%). Initial management consisted of chemotherapy (CHT) alone in 21 (56.8%), radiation therapy (RT) alone in 2 patients (5.4%), RT and rituximab in 1 (2.7%), CHT and RT in 7 (18.9%), and observation in 6 (16.2%). RT was to a median dose of 30.6 Gy (range, 23.4-44.0 Gy). At a median follow-up of 69 months (range, 8-157 months), 5-year PFS and OS were 70.4% and 94.4%, respectively. Although the 5-year PFS of those observed was worse than for those who received therapy (33.3% vs. 77.6%; P = .011), that did not translate into an OS difference. Patients who received RT as part of upfront management had a 100% local control (LC) rate and a trend toward improved 5-year PFS (90% vs. 62.2%; P = .067). Early stage E-FL is an indolent disease and is associated with excellent OS. Treatment strategies should be individualized with RT prioritized when LC is a significant goal.

Identifiants

pubmed: 30935940
pii: S2152-2650(18)31509-X
doi: 10.1016/j.clml.2019.02.011
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

381-389

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Therese Andraos (T)

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

Zeina Ayoub (Z)

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

Loretta Nastoupil (L)

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

Chelsea Pinnix (C)

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

Sarah Milgrom (S)

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

Jillian Gunther (J)

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

Sweet Ping Ng (SP)

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

Nathan Fowler (N)

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

Sattva Neelapu (S)

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

Felipe Samaniego (F)

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

Bouthaina Dabaja (B)

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

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