Hyperthermic intraperitoneal chemotherapy as consolidation treatment of advanced stage ovarian cancer
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ObjectiveTo investigate the therapeutic efficacy of hyperthermic intraperitoneal chemotherapy (HIPEC) as consolidationtreatment after completing first-line treatment in patients with advanced ovarian cancer. MethodsA retrospective chart review was conducted on patients treated at the Comprehensive Gynecologic Cancer Centerbetween January 2014 and 2019. Based on the inclusion criteria, 24 eligible patients who received HIPEC (paclitaxel175 mg/m2, for 90 minutes, at 42°C) (HIPEC group) as consolidation treatment after terminating the adjuvantchemotherapy were identified. Another 24 patients who met the inclusion criteria and did not receive HIPEC werematched, representing the non-HIPEC group. Disease-free survival (DFS) and overall survival (OS) were examinedbetween the two groups. ResultsThe median DFS was 28.7 and 24.2 months in the HIPEC and non-HIPEC groups, respectively (P=0.688). The 3-yearDFS rates in the HIPEC and non-HPEC groups were 39.5% and 32.6%, respectively. However, the median OS was notdetermined. The 5-year OS rates in the HIPEC and non-HIPEC groups were 86.2% and 81.3%, respectively (P=0.850). One patient developed grade 3 neutropenia. Other patients experienced mild adverse events after HIPEC. ConclusionThis study suggests that consolidation HIPEC could not support the survival benefit after completing the first-linetreatment for patients with advanced ovarian cancer, although no severe specific safety issues were found. Therefore,randomized trials evaluating consolidation HIPEC for the management of ovarian cancer are warranted.
Abstract
ObjectiveTo investigate the therapeutic efficacy of hyperthermic intraperitoneal chemotherapy (HIPEC) as consolidationtreatment after completing first-line treatment in patients with advanced ovarian cancer. MethodsA retrospective chart review was conducted on patients treated at the Comprehensive Gynecologic Cancer Centerbetween January 2014 and 2019. Based on the inclusion criteria, 24 eligible patients who received HIPEC (paclitaxel175 mg/m2, for 90 minutes, at 42°C) (HIPEC group) as consolidation treatment after terminating the adjuvantchemotherapy were identified. Another 24 patients who met the inclusion criteria and did not receive HIPEC werematched, representing the non-HIPEC group. Disease-free survival (DFS) and overall survival (OS) were examinedbetween the two groups. ResultsThe median DFS was 28.7 and 24.2 months in the HIPEC and non-HIPEC groups, respectively (P=0.688). The 3-yearDFS rates in the HIPEC and non-HPEC groups were 39.5% and 32.6%, respectively. However, the median OS was notdetermined. The 5-year OS rates in the HIPEC and non-HIPEC groups were 86.2% and 81.3%, respectively (P=0.850). One patient developed grade 3 neutropenia. Other patients experienced mild adverse events after HIPEC. ConclusionThis study suggests that consolidation HIPEC could not support the survival benefit after completing the first-linetreatment for patients with advanced ovarian cancer, although no severe specific safety issues were found. Therefore,randomized trials evaluating consolidation HIPEC for the management of ovarian cancer are warranted.
참고문헌 (23)
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