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Treatment Outcomes in Patients with Conjunctival Mucosa-Associated Lymphoid Tissue (MALT) Lymphoma.
Matsuo, Yu; Monden, Yu; Sasaki, Kensuke; Akune, Hodaka; Ikeda, Shuntaro; Ishio, Daiki; Murotani, Kenta; Nagafuji, Koji; Yoshida, Shigeo.
Afiliación
  • Matsuo Y; Department of Ophthalmology, Kurume University School of Medicine, Kurume, Japan.
  • Monden Y; Department of Ophthalmology, Kurume University School of Medicine, Kurume, Japan.
  • Sasaki K; Department of Ophthalmology, Kurume University School of Medicine, Kurume, Japan.
  • Akune H; Department of Ophthalmology, Kurume University School of Medicine, Kurume, Japan.
  • Ikeda S; Department of Ophthalmology, Kurume University School of Medicine, Kurume, Japan.
  • Ishio D; Department of Ophthalmology, Kurume University School of Medicine, Kurume, Japan.
  • Murotani K; Biostatistics Center, Kurume University, Kurume, Japan.
  • Nagafuji K; Department of Hematology and Oncology, Kurume University School of Medicine, Kurume, Japan.
  • Yoshida S; Department of Ophthalmology, Kurume University School of Medicine, Kurume, Japan.
Clin Ophthalmol ; 18: 1999-2007, 2024.
Article en En | MEDLINE | ID: mdl-39005589
ABSTRACT

Purpose:

To report the outcomes of different therapies in patients with conjunctival mucosa-associated lymphoid tissue (MALT) lymphoma. Patients and

Methods:

This retrospective study included patients diagnosed with conjunctival MALT lymphoma between August 2000 and April 2022. Patients were classified into three groups according to their treatment an observation group, a radiation therapy (RT) group, and a rituximab group (rituximab with or without chemotherapy). We analyzed overall survival (OS), overall, local, and systemic relapse-free survival (RFS), and adverse events after treatment.

Results:

This study included 15 patients (22 eyes). The 10-year OS was 100%. The 2-, 5-, and 10-year overall RFS rates were 80.1%, 41.2%, and 41.2% in all patients, respectively. The 2- and 5-year local RFS rates in the observation group were 100% and 0%, respectively. The 2-, 5-, and 10-year local RFS rates were 87%, 87%, and 87% in the RT group and 83%, 67%, and 67% in the rituximab group, respectively. The 2- and 5-year systemic RFS rates in the observation group were both 100%, and the 2-, 5-, and 10-year systemic RFS rates were 92%, 55%, and 55% in the RT group, and 100%, 60%, and 60% in the rituximab group, respectively. After RT, 53.3% of the eyes developed cataracts and 75% of these were treated with cataract surgery. In addition, 53.3% of the eyes developed dry eyes and were treated with eye drops. Rituximab with or without chemotherapy resulted in some systemic adverse events, but these improved following symptomatic therapies.

Conclusion:

RT resulted in good local control of conjunctival MALT lymphoma; however, systemic relapse may occur during long-term follow-up. Local and/or systemic relapse may also occur during long-term follow-up in patients treated by observation or rituximab with or without chemotherapy. Patients with conjunctival MALT lymphoma should be followed-up carefully for as long as possible after treatment.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Ophthalmol Año: 2024 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Nueva Zelanda

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Ophthalmol Año: 2024 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Nueva Zelanda