Chest
Volume 110, Issue 4, October 1996, Pages 1115-1117
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Selected Reports: Articles
Retreatment of Recurrent Invasive Thymoma with Platinum, Doxorubicin, and Cyclophosphamide

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Invasive thymoma recently has been shown to be sensitive to combination chemotherapy and in some cases to be relatively indolent. Two cases of extensive thymoma which responded to primary treatment with a combination of a platinum compound (carboplatin or cisplatin), doxorubicin (Adriamycin), and cyclophosphamide (or PAC) are described. Tumor progression occurred 14 (case 1) and 60 months (case 2) after completion of initial PAC therapy and was treated with the same regimen resulting in a second remission, which lasted 6 months in case 1 and is continuing at 8 months in case 2. Similar reports of secondary responses using the same chemotherapy have been described in breast, lung, and ovarian cancers, as well as in Hodgkin's lymphomas. Our observations suggest that retreatment with the same platinum-based regimen should be considered in patients who have progressive thymomas following a previous chemotherapeutic response and a disease-free interval of greater than 12 months.

Section snippets

Case 1

A 26-year-old Asian man was first seen at our institution in November 1978 with a diagnosis of myasthenia gravis requiring therapy with prednisone and subsequently a thymectomy in December 1978. During the next decade, he suffered recurrent upper respiratory tract infections and myasthenic exacerbations. He was readmitted to this hospital in May of 1992 for productive cough and fever. A chest radiograph done at this time showed an anterior mediastinal mass, and a subsequent CT scan confirmed

Discussion

Recently, it has become apparent that invasive thymoma is relatively sensitive to combination chemotherapy and that survival is relatively long. In two fairly large series using the PAC regimen or a combination of cisplatin, doxorubicin, vincristine, and cyclophosphamide, overall response rates ranged from 70 to 91.8%, with median durations of response averaging 11.9 months and median survival ranging from 15 to 37.7 months.3,4 Recently, PAC with etoposide and concurrent granulocyte

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revision accepted May 15.

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