We report the case of a 65 years old woman with a NHL, CD20 +, BCL-2 negative, Grade III, CS: IVBX, FLIPI High Risk, diagnosed on September 2005. The patient was treated with several chemotherapy regimens (CHOP, chlorambucil/prednisone, cyclophosphamide/prednisone), while on treatment a large pleural effusion was found on a chest X-ray. On pleural fluid cytology we observed numerous abnormal lymphocytes. We did repeated thoracocentesis without success, finally a pleural tube was inserted and intrapleural bleomycin instilled, again with no success (Table 1). Six weeks later, after signing informed consent, we administered 50 mg of intrapleural R (50 mg in 50 cc of SS 0.9%) without immediate or delayed adverse events. On day +4 a new chest X-ray showed marked improvement. We planned to repeat the dose every week × 4, unfortunately the patient could not afford it. After seven months the patient is asymptomatic and without recurrence of the pleural effusion.

Table 1

Date (2007)Fluid drained (ml)Action
September 12 Dyspnea  
September 21 1,500  
October 4 1,500  
October 6 570  
October 8 400  
October 12 20 Bleomycin 10 U 
November 6 Dyspnea/1,300  
November 9 40  
November 16 400  
November 17 200  
November 20 100 Rituximab 50 mg 
Date (2007)Fluid drained (ml)Action
September 12 Dyspnea  
September 21 1,500  
October 4 1,500  
October 6 570  
October 8 400  
October 12 20 Bleomycin 10 U 
November 6 Dyspnea/1,300  
November 9 40  
November 16 400  
November 17 200  
November 20 100 Rituximab 50 mg 

Discussion Although the pharmacology of IV R is welll known, there is scarce information about dosage, penetration into the tissues and efficacy of intracavitary R. It is likely that the intrapleural instillation of R was effective in the control of this complication in a definitive way, without adverse effects, Our case supports the results reported by Schmidt et al (Table 2). The mechanism of action at the local site is not known, but it could be the same as described with the systemic use. Pleural effusion secondary to refractory lymphoma is a rare complication, we propose the integration of an international registry of this cases to study the pharmacokinetics, pharmacodynamics, efficacy and safety of intrapleural rituximab.

Table 2

FeaturesOur patientSchmidt Patient
Age age 65 years 57 years 
Diagnosis Follicular NHL, Grado II Lymphoplasmacytic NHL 
No. Previous Therapy 
Effusion therapy Thoracocentesis and drainage by pleurostomy Thoracocentesis 
Rituximab Dose 50mg, single dose 50mg day 1 200mg day 2 400mg day 3 
Time to Response 4 days 3 days 
FeaturesOur patientSchmidt Patient
Age age 65 years 57 years 
Diagnosis Follicular NHL, Grado II Lymphoplasmacytic NHL 
No. Previous Therapy 
Effusion therapy Thoracocentesis and drainage by pleurostomy Thoracocentesis 
Rituximab Dose 50mg, single dose 50mg day 1 200mg day 2 400mg day 3 
Time to Response 4 days 3 days 

Disclosures: No relevant conflicts of interest to declare.

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