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Concomitant chemobrachyradiotherapy with ifosfamide and cisplatin followed by consolidation chemotherapy in the treatment of locally advanced adenocarcinoma or adenosquamous carcinoma of the cervix uteri

  • E. Vrdoljak1,*,
  • T. Boraska Jelavic1
  • Z. Saratlija-Novakovic1
  • W. Hamm2

1Center of Oncology, Clinical Hospital Split, Split, Croatia

2Baxter Oncology GmbH, Frankfurt, Gennany

DOI: 10.12892/ejgo200506602 Vol.26,Issue 6,November 2005 pp.602-604

Published: 10 November 2005

*Corresponding Author(s): E. Vrdoljak E-mail:

Abstract

The optimal treatment of women with locally advanced adenocarcinoma or adenosquamous carcinoma of the cervix uteri is still undefined. We report a series of four consecutive patients with locally advanced adeno- or adenosquamous carcinomas of the uterine cervix (FIGO Stages IB-IIIB) treated by concomitant chemobrachyradiotherapy with ifosfamide and cisplatin followed by one to four cycles of consolidation chemotherapy with the same drug combination. After completion of this treatment all patients showed complete clinical remission. Now, after a median follow-up of 40 (range: 13.5-61) months all patients still present with no evidence of disease. Despite the low number of patients in this series we may conclude that concomitant chemobrachyradiotherapy with ifosfamide and cisplatin followed by consolidation chemotherapy with the same drug combination is an efficacious treatment of patients with locally advanced adeno- or adenosquamous carcinomas of the cervix uteri.

Keywords

Concomitant chemoradiation; Ifosfamide; Cisplatin; Consolidation chemotherapy; Adenocarcinoma of the cervix uteri; Adenosquamous carcinoma of the cervix uteri

Cite and Share

E. Vrdoljak,T. Boraska Jelavic,Z. Saratlija-Novakovic,W. Hamm. Concomitant chemobrachyradiotherapy with ifosfamide and cisplatin followed by consolidation chemotherapy in the treatment of locally advanced adenocarcinoma or adenosquamous carcinoma of the cervix uteri. European Journal of Gynaecological Oncology. 2005. 26(6);602-604.

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