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Clinical Trial
. 2000 Mar-Apr;47(32):378-82.

Stop-flow in mediastinum and thorax for resistant lymphoma

Affiliations
  • PMID: 10791194
Clinical Trial

Stop-flow in mediastinum and thorax for resistant lymphoma

S Guadagni et al. Hepatogastroenterology. 2000 Mar-Apr.

Erratum in

  • Hepatogastroenterology 2000 Sep-Oct;47(35):following table of contents. Stefano, G [corrected to Guadagni, S]; Filippo, R [corrected to Russo, F]; Giuseppe, A [corrected to Abate, G]; Tullio, P [corrected to Pozone, T]; Benita, C [corrected to Capannolo, B]; Luca, M [corrected to Marsili, L]; Valfredo, D [corrected to D'Alessa

Abstract

Background/aims: Management of patients with heavily pretreated malignant lymphoma failing frontline treatment and salvage high-dose chemotherapy and autologous peripheral stem cell rescue, is problematic. A pilot study was conducted to evaluate isolated thoracic perfusion of drugs by means of stopflow technique.

Methodology: Six patients were enrolled in the study; diagnoses included 4 advanced Hodgkin's disease, 1 primary mediastinal B-cell lymphoma, and 1 anaplastic large cell lymphoma. Patients were aged 18-37 years; 4 presented with bulky mediastinum. They had never achieved a complete response since all had progressed from front-line treatment, and 3 had even failed salvage high-dose chemotherapy with autologous peripheral stem cell rescue. Cisplatin (100 mg/m2) and melphalan (35 mg/m2) were used. Carmustine (100 mg/m2) were added to these 2 drugs and cytarabine (2000 mg/m2) in patients not previously treated by carmustine, etoposide, cytarabine, and melphalan. Epidoxorubicin (70 mg/m2) was added in patients who previously received a suboptimal dosage of antracycline. Drugs were delivered monthly via aortic perfusion performed by means of Aigner's stop-flow technique.

Results: Overall 13 cycles of perfusional chemotherapy were administered with a median number of 2 cycles. During the procedures there were no technical, hemodynamic, or vascular complications, and no deaths occurred during surgery. After 1 month, 6 (100%) objective responses after isolated thoracic perfusion were recorded, 3 (50%) of which were complete. Tolerance to therapy was excellent. Hematological toxicity was mild and transfusional support was needed only in one course. At the last follow-up, 2 patients are alive (1 complete response and 1 very good partial response, maintained).

Conclusions: This new therapeutical approach seems very active in recurrent/refractory malignant lymphoma and may play an important role in this setting.

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