High-dose carboplatin with etoposide in patients with recurrent thymoma: the Indiana University experience

Citation
N. Hanna et al., High-dose carboplatin with etoposide in patients with recurrent thymoma: the Indiana University experience, BONE MAR TR, 28(5), 2001, pp. 435-438
Citations number
22
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
Journal title
BONE MARROW TRANSPLANTATION
ISSN journal
02683369 → ACNP
Volume
28
Issue
5
Year of publication
2001
Pages
435 - 438
Database
ISI
SICI code
0268-3369(200109)28:5<435:HCWEIP>2.0.ZU;2-Y
Abstract
Thymoma is a chemotherapy-sensitive tumor with a 30-50% 5-year survival in previously untreated patients. Unfortunately, durable CRs with salvage chem otherapy are rarely observed. We initiated a phase II trial of high-dose ca rboplatin and etoposide in patients with relapsed thymoma or thymic carcino ma. All patients had progressive disease (PD) after initial or salvage chem otherapy, but were not cisplatin-refractory. PBSCs were mobilized using 10 mug/kg/day G-CSF. Patients received carboplatin 700 mg/m(2) and etoposide 7 50 mg/m(2) i.v. on days -5, -4, -3. Five patients were enrolled and evaluat ed after tandem transplants 4 weeks apart. All patients had pleural-based a nd lung parenchymal metastasis, one or two prior surgeries and two or more courses of prior cisplatin-based chemotherapy regimens. Chemotherapy was we ll tolerated, although grade IV hematological toxicity occurred in all pati ents. Progression-free survival following HDC ranged from 3.5 to 16.5 month s. One patient maintained a CR for 12.8 months, then died from an unrelated cause. With a minimum of 2 years follow-up for all patients, three of five patients remain alive at 26+, 36+, and 49+ months. High-dose carboplatin a nd etoposide in relapsed thymoma is feasible with acceptable toxicity, howe ver, these limited data do not appear superior to standard-dose salvage the rapy.