Objective: Phase 3 trials have demonstrated a survival
advantage for patients with optimally debulked epithelial ovarian
cancer who received intravenous (IV) and intraperitoneal (IP)
chemotherapy compared with IV therapy alone. This was despite a
significant proportion of patients in the IV/IP arms not completing all 6
planned cycles. Our objective was to evaluate the prognostic
significance of the number of IV/IP cycles administered.
Methods/Materials: Data were analyzed for all patients
with stage III to IV epithelial ovarian cancer who underwent optimal
primary cytoreduction followed by 1 or more cycles of IV/IP chemotherapy
from January 2005 to July 2011 at our institution. A landmark analysis
was performed to associate progression-free survival (PFS) and overall
survival (OS) with the number of IV/IP cycles given.
Results: We identified 201 patients; 26 (13%) received
1 to 2 cycles of IV/IP chemotherapy, 41 (20%) received 3 to 4 cycles,
and 134 (67%) received 5 to 6 cycles. The 5-year PFS for patients who
received 1 to 2, 3 to 4, and 5 to 6 cycles was 18%, 29%, and 17%,
respectively. The 5-year OS for patients who received 1 to 2, 3 to 4,
and 5 to 6 cycles was 44%, 54%, and 57%, respectively. There was no
significant difference in PFS (P = 0.31) or OS (P =
0.14) between the 3 groups. The most common reason for discontinuing
IV/IP therapy was treatment-related toxicity (77%). Postoperative
complications were the most common reason for not initiating IV/IP
therapy (42%) in patients who subsequently transitioned to it.
Conclusions: We did not detect a significant survival
difference between patients who received 1 to 2, 3 to 4, or 5 to 6 IV/IP
chemotherapy cycles. Women may still derive a survival benefit if they
receive fewer than 6 IV/IP cycles.
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