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J L Rodríguez García

Publications and source records attributed to J L Rodríguez García.

3 recordsLinked to original sources

[The treatment of large-cell non-Hodgkin's lymphomas with the MACOP-B protocol].

BACKGROUND: To investigate the results of the treatment of large-cell non-Hodgkin's lymphomas (LCNHL) with the MACOP-B chemotherapy protocol. METHODS: 20 patients with the following inclusion criteria were treated: LCNHL with a definite majority of large lymphoid cells and absence of previous therapy, HIV infection or severe underlying diseases. RESULTS: Three patients died during therapy and 15 (75%) achieved a complete remission. Actuarial survival after 36 months (0.66) was significantly better (p = 0.05) than that of a comparable historical series of LCNHL treated with CHOP (0.28). Age, stages III-IV, B symptoms, large lymphatic mass (LLM) and bone marrow infiltration did not negatively affect survival. The toxicity of the MACOP-B protocol was high: mucositis (65%), cytopenia (55%), neuropathy (40%), complications of steroid therapy (15%), and mortality directly related with therapy in 15%. Residual masses were found after therapy in 7% (70%) with BD, which were localized in lymphoid areas or in parenchyma (spleen and kidney). Surgical exploration showed that the residual masses were not tumoral in three cases, and in another three magnetic resonance suggested inactive disease. CONCLUSIONS: The MACOP-B protocol is highly effective for the treatment of LCNHL. The essential prognostic factor for survival in these NHL appears to be the cell composition with a great majority of large cells.

Antineoplastic Combined Chemotherapy Protocols↗

[Raynaud's phenomenon].

Raynaud's phenomenon (RP) is characterized by paroxysmal ischemic crisis of the hands and feet provoked by physical or emotional stimuli. The RP's prevalence is estimated between 4 and 5% of the general population, accompanying or not other conditions, or preceding in years the appearance of various connective tissue diseases. We have to consider, in its pathogenesis, alterations in the vascular tone or intraluminal thromboembolic phenomena. The diagnosis is based on the clinical picture since there are no specific tests to detect primary RP. Therapeutic measures include: change in lifestyle, vasodilator drugs and anti-platelet aggregation drugs, plasmapheresis and surgery. Treatment should be individualized.

Humans↗