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Carboplatin and chlorambucil combination chemotherapy as treatment for patients with ovarian cancer
  1. B. D. Evans*,**,
  2. P. Chapman,
  3. P. Dady,
  4. G. Forgeson*,
  5. D. Perez§,
  6. M. Mckeage,†† and
  7. P. Mitchell
  1. * Oncology Unit, Palmerston North Hospital, Palmerson North;
  2. Oncology Unit, Waikato Hospital, Hamilton;
  3. Oncology Unit, Wellington Hospital, Wellington;
  4. § Oncology Unit, Dunedin Hospital, Dunedin; and
  5. Oncology Unit, Auckland Hospital, Auckland, New Zealand
  6. ** Present address: Oncology Unit, Auckland Hospital, Auckland, New Zealand.
  7. †† Present address: Institute of Cancer Research, Downs Road, Sutton, Surrey, England.
  1. Address for correspondence: B. D. Evans, Oncology Unit, Auckland Hospital, Park Road, Auckland, New Zealand.

Abstract

Fifty-six patients with ovarian cancer (three stage IC, nine stage II, 33 stage III and II stage IV) were treated with carboplatin 350 mg m−2 i.v. day 1 and chlorambucil orally 0.15 mg kgm−1 days 1–7 inclusive, repeated every 28 days for eight courses. The regimen was well tolerated and was virtually free of nephro- and neurotoxicity. Grade III or IV hematology toxicity occurred in 18 patients but only 31 or 330 courses administered were delayed. Of 40 assessable patients eight achieved a clinical/radiologic complete response and 17 a clinical/radiologic partial response. Actuarial survival at 50 months was 65% for stage II patients, 27% for stage III patients and no stage IV patients survived beyond 20 months. Forty-two per cent of patients with residual disease less 2 cm survived 50 months, compared with 44% of patients with moderate volume (2–5 cm) residual disease and 6% of patients with bulk residual disease. This is an active, well tolerated regimen. However, only patients with small volume residual disease have a significant chance of prolonged survival.

  • chemotherapy
  • ovarian cancer.

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