Weekly paclitaxel in patients with CAP-resistant advanced or recurrent endometrial carcinoma: a series of four patients

Int J Clin Oncol. 2005 Aug;10(4):272-5. doi: 10.1007/s10147-005-0482-0.

Abstract

We evaluated the feasibility of weekly paclitaxel in patients with recurrent or advanced endometrial carcinoma who had failed treatment with cyclophosphamide, doxorubicin, and cisplatin (CAP). We treated four patients with CAP-resistant recurrent or advanced endometrial carcinoma with paclitaxel. Paclitaxel (80 mg/m(2); infused over 1 h) was administered weekly for a maximum of 18 weeks, unless disease progression or intractable toxicity developed. A complete response was observed in one patient and a partial response in two patients. Disease progression was found in one patient. Two patients developed grade 3 leukopenia or neutropenia. Neurotoxicity for all patients was within grade 1. Outpatient treatment with weekly paclitaxel was well-tolerated and feasible for patients with CAP-resistant recurrent or advanced endometrial carcinoma. Further trials to confirm the efficacy and toxicity of weekly paclitaxel are warranted.

Publication types

  • Case Reports

MeSH terms

  • Adenocarcinoma, Clear Cell / drug therapy
  • Adenocarcinoma, Clear Cell / secondary
  • Adenocarcinoma, Mucinous / drug therapy
  • Adenocarcinoma, Mucinous / secondary
  • Adenocarcinoma, Papillary / drug therapy
  • Adenocarcinoma, Papillary / secondary
  • Aged
  • Antineoplastic Agents, Phytogenic / therapeutic use*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Carcinoma, Endometrioid / drug therapy*
  • Carcinoma, Endometrioid / pathology
  • Cisplatin / therapeutic use
  • Cyclophosphamide / therapeutic use
  • Cystadenocarcinoma, Serous / drug therapy
  • Cystadenocarcinoma, Serous / secondary
  • Doxorubicin / therapeutic use
  • Drug Resistance, Neoplasm*
  • Feasibility Studies
  • Female
  • Humans
  • Infusions, Intravenous
  • Maximum Tolerated Dose
  • Middle Aged
  • Neoplasm Recurrence, Local / drug therapy*
  • Neoplasm Recurrence, Local / pathology
  • Paclitaxel / therapeutic use*
  • Salvage Therapy
  • Survival Rate
  • Treatment Outcome

Substances

  • Antineoplastic Agents, Phytogenic
  • Doxorubicin
  • Cyclophosphamide
  • Paclitaxel
  • Cisplatin

Supplementary concepts

  • CISCA protocol