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Evaluation of non-completion of intraperitoneal chemotherapy in patients with advanced epithelial ovarian cancer
被引:6
|作者:
Chambers, Laura Moulton
[1
]
Son, Ji
[2
]
Radeva, Milena
[3
]
DeBernardo, Robert
[1
]
机构:
[1] Cleveland Clin, Div Gynecol Oncol, Obstet Gynecol & Womens Hlth Inst, Desk A81,9500 Euclid Ave, Cleveland, OH 44195 USA
[2] Cleveland Clin, Obstet Gynecol & Womens Hlth Inst, Cleveland, OH 44106 USA
[3] Cleveland Clin, Quantitat Hlth Sci Dept, Cleveland, OH 44106 USA
关键词:
Ovarian Cancer;
Adjuvant Chemotherapy;
Intraperitoneal Infusion;
STAGE-III OVARIAN;
CYTOREDUCTIVE SURGERY;
PRIMARY PERITONEAL;
COMPLICATIONS;
TOXICITY;
PACLITAXEL;
CISPLATIN;
DISCHARGE;
OUTCOMES;
TRIAL;
D O I:
10.3802/jgo.2019.30.e93
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Objective: To identify factors associated with non-completion of intraperitoneal with intravenous chemotherapy [IP/IV] in women with epithelial ovarian cancer (EOC). Methods: This was an Institutional Review Board approved, retrospective cohort study in women with stage III EOC following optimal cytoreductive surgery (CRS) (<1 cm) followed by IP/IV chemotherapy from 2000-2016. Demographic, surgical, and oncologic variables were collected. Pearson chi(2) test and 2 sample t-test evaluated for variables associated with IP/IV chemotherapy completion. Kaplan-Meier survival analysis was performed for progressionfree survival (PFS) and overall survival (OS). Results: Of 96 women, 71.9% (n=69) completed 6 cycles of IP/IV chemotherapy. The majority had high grade serous histology (n=82; 85.4%) and stage IIIC disease (n=83; 86.5%). Common reasons for IP/IV chemotherapy discontinuation were grade 3-4 gastrointestinal (n=10; 37.0%), neurologic (n=6; 22.2%), hematologic (n=3; 11.1%), renal toxicities (n=3; 11.1%) and port infections (n=3; 11.1%). Incidence of IP port complications was 20.8% (n=20). Port complications (48.0% vs. 11.6%; p<0.001) and hospitalization during chemotherapy (29.6% vs. 2.9%; p<0.001) were more frequent in patients who discontinued IP/IV chemotherapy. Patients who completed IP/IV chemotherapy had higher rates of home discharge following CRS (92.2% vs. 72.0%; p<0.01) and lower Eastern Cooperative Oncology Group (ECOG) score (0 vs. 1.0; p=0.04). There was no significant difference in PFS (p=0.51) nor OS (p=0.38) between the cohorts. Conclusion: In this series, the rate of IP/IV chemotherapy completion is high. Non-home discharge and higher ECOG status following CRS are associated with IP/IV chemotherapy non-completion and should be considered in treatment planning.
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页数:13
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