Intraperitoneal chemotherapy for advanced epithelial ovarian malignancy: Lessons learned
| Autor: | Warren S. W. Chan, Penelope Blomfield, Alison Brand, Michael Bunting |
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| Rok vydání: | 2009 |
| Předmět: |
Adult
Oncology medicine.medical_specialty Paclitaxel medicine.medical_treatment Antineoplastic Agents Cohort Studies Route of administration Internal medicine Humans Medicine Infusions Parenteral Adverse effect Aged Retrospective Studies Ovarian Neoplasms Chemotherapy business.industry Australia Obstetrics and Gynecology Common Terminology Criteria for Adverse Events General Medicine Middle Aged medicine.disease Surgery Treatment Outcome Chemotherapy Adjuvant Toxicity Female Cisplatin business Ovarian cancer Complication Adjuvant |
| Zdroj: | Australian and New Zealand Journal of Obstetrics and Gynaecology. 49:667-671 |
| ISSN: | 1479-828X 0004-8666 |
| Popis: | Background: The administration of intraperitoneal (IP) chemotherapy as first-line adjuvant treatment for women with optimally debulked advanced ovarian malignancy results in improved median and overall survival when compared with intravenous (IV) chemotherapy. However, the number of adverse events and toxicities are increased in patients treated with IP chemotherapy. In addition, the administration of IP chemotherapy is technically more challenging and the schedule is more demanding in terms of time and resources. Aims: We report on our initial experience with the administration of IP chemotherapy at two gynaecological oncology units in Australia. Methods: We collected retrospective data from a series of 23 women undergoing IP chemotherapy as adjuvant treatment for advanced ovarian cancer. In addition to standard (Common Terminology Criteria for Adverse Events v3.0, CTCAE) toxicity data, we collected technical data specific to the administration of IP chemotherapy. Results: The average number of IP chemotherapy cycles received was 4.3. Forty-three per cent of patients received all six planned IP chemotherapy cycles. Thirty-nine per cent of patients discontinued their IP treatment. Of those, 22% were discontinued because of drug-related toxicities and the remaining 17% experienced a port complication or toxicity directly related to the route of administration. Conclusions: This study demonstrates the feasibility and practicality of and lessons learned from initial experiences with IP chemotherapy for ovarian cancer in Australia. |
| Databáze: | OpenAIRE |
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