Objective of this trial is to establish the efficacy of an upfront targeted therapy consisting of Chlamydophila psittaci (Cp)-eradicating therapy with prolonged administration of doxycycline followed by eradication monitoring and antibiotic re-treatment at infection re-occurrence in patients with newly diagnosed ocular adnexae marginal zone lymphoma The primary endpoint is the 2-year progression-free survival (PFS) of patients with newly diagnosed stage-IE lymphoma treated with the experimental strategy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
34
All enrolled patients will be treated with doxycycline 100 mg bid daily, orally, for four weeks followed by four weeks rest, repeated for three cycles. Response will be assessed by MRI (magnetic resonance imaging) and ophthalmologic examination at the end of the planned treatment. Patients who will achieve complete response, partial response or have a stable disease at 3 months from upfront doxycycline will be monitored for infection re-occurrence and assessed for response with MRI and ophthalmologist evaluation every six months for the first five years.
AO Ospedali Riuniti Papardo Piemonte
Messina, Italy
Ospedale San Raffaele
Milan, Italy
Ematologia
Parma, Italy
Ospedale Civile
Piacenza, Italy
Università La Sapienza
Rome, Italy
Molinette 1
Torino, Italy
Ospedale dell'Angelo
Venezia, Italy
progression-free survival (PFS)
from the date of the start of treatment to relapse, progression or death, or to the last date of follow-up
Time frame: 2-year from start of treatment
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