Abstract

Background. The survival rate of patients with ovarian malignancies depends on the prevalence of the tumor process, the volume of surgical treatment, and the size of the residual tumor. At the first stage, an «aggressive» surgical tactic of removing all macroscopically determined tumor foci with subsequent antitumor drug therapy is recommended. However, the results of treatment remain unsatisfactory, which dictates the need to search for new methods of treatment.Objective: to evaluate the effectiveness of implantable port systems for intraperitoneal chemotherapy administration in the treatment of patients with advanced stages of ovarian cancer.Materials and methods. 37 cases of stage IIIC ovarian cancer were studied for the period 2018–2019. At the first stage of treatment, a cytoreductive operation was performed. At the second stage, the patients were randomly randomized into three groups: group 1 (n = 9) – installation of a port system + hyperthermic intraperitoneal chemoperfusion followed by intraperitoneal chemotherapy; group 2 (n = 11) – hyperthermic intraperitoneal chemoperfusion followed by systemic intravenous chemotherapy; group 3 (n = 17) – control group, intravenous administration of antitumor drugs. The observation period is 27 months. In the study groups, the indicators of age distribution, the degree of malignancy of the neoplasm, the volume of the residual tumor, and the relapse-free survival were analyzed.Results. Trends towards differences in progression-free survival were found in all study groups. In group 1, there was no relapse in all patients. In group 2, relapses amounted to 18.2 %, in group 3–23.5 %. G3 ovarian cancer (6 (66.7 %) and 6 (54.5 %) cases, respectively) prevailed in groups 1 and 2; G1 ovarian cancer (9 (52.9 %) cases) prevailed in group 3. Discussion. Features of the chemical composition and method of administration of the drug increase the effectiveness of local exposure to tumor cells. The introduction of cytostatic agents into the abdominal cavity leads to minimal systemic toxicity, which exceeds the results of standard intravenous therapy.Conclusion. An advantage in the relapse-free survival of patients after hyperthermic intraperitoneal chemoperfusion in combination with an implantable port system was found in comparison with standard methods of treatment.

Highlights

  • Materials and methods. 37 cases of stage IIIC ovarian cancer were studied for the period 2018–2019

  • The patients were randomly randomized into three groups: group 1 (n = 9) – installation of a port system + hyperthermic intraperitoneal chemoperfusion followed by intraperitoneal chemotherapy; group 2 (n = 11) – hyperthermic intraperitoneal chemoperfusion followed by systemic intravenous chemotherapy; group 3 (n = 17) – control group, intravenous administration of antitumor drugs

  • Trends towards differences in progression-free survival were found in all study groups

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Summary

Оригинальные статьи

Цель исследования – провести оценку эффективности применения имплантируемых порт-систем для введения химиотерапии интраперитонеально в лечении пациенток с распространенными стадиями рака яичников. На 2‐м этапе пациентки случайным образом были рандомизированы на 3 группы: 1-я группа (n = 9) – установка порт-системы + проведение гипертермической интраперитонеальной химиотерапии; 2-я группа (n = 11) – проведение гипертермической интраперитонеальной химиотерапии с последующей системной внутривенной химиотерапией; 3-я группа (n = 17) – группа контроля, введение противоопухолевых препаратов внутривенно. Введение цитостатических агентов в брюшную полость приводит к минимальной системной токсичности, что превосходит результаты стандартной внутривенной терапии. Обнаружено преимущество по безрецидивной выживаемости пациентов после проведения гипертермической интраперитонеальной химиотерапии в сочетании с имплантируемой порт-системой в сравнении со стандартными методами лечения. Роль гипертермической внутрибрюшинной химиотерапии в комбинации с интраперитонеальной порт-системой в лечении пациенток с распространенными формами рака яичников.

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