Testicular cancer patients refractory or in relapse after primary
chemotherapy have < or =25% 5-year progression-free survival with salvage. To improve prognosis, patients entered a phase I/II tandem dose-escalation trial of
carboplatin (1500-2100 mg/m(2)) and
etoposide (1200-2250 mg/m(2)) with ABMT. Patients were eligible for a second cycle if
disease progression was absent and performance status allowed. From August 1990 to June 1998, 29 males (25 NSGCT) were treated. At the time of ABMT, 10 were chemosensitive, four were chemoresistant, and 10 were absolutely refractory to
platinum. Disease status (no. patients) at transplant: primary refractory disease (six), first relapse (10), second relapse (eight), third relapse (five). Fifteen (52%) received both transplants. Treatment-related mortality was 10%. Best response after ABMT included: two CR, one CR surgically NED, five PR, three PR surgically NED, seven SD, and eight PD. Eight (28%) patients are continuously progression-free a median 60 months (range, 31-93) from first ABMT. Three
seminoma patients remain progression-free. Of five long-term NSGCT survivors, four were treated in first relapse with
platinum-sensitive disease. Eighteen relapses occurred a median of 4 months after ABMT I (two late relapses at 28 and 44 months). The median PFS and OS for the whole group are 4 and 14 months, respectively. Patients with relapsed/ refractory
testicular cancer benefit most from ABMT if they have
platinum-sensitive disease in first relapse. Patients who do poorly despite ABMT have a mediastinal primary site, true
cisplatin-refractory disease,
disease progression prior to ABMT, and/or markedly elevated betaHCG at ABMT. New treatment modalities are needed for the latter group.