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Completed

NCT Number: NCT00190489

A Trial of Doxorubicin/Cyclophosphamide (AC), Docetaxel (D), and Alternating AC and D for Metastatic Breast Cancer

To investigate the clinical benefits of Docetaxel or alternating AC-Docetaxel in comparison with standard AC for metastatic breast cancer

Completed

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Key information

Age range

20 year–75 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

National Cancer Center Hospital

Chuo-ku, Tsukiji, 5-1-1, Tokyo, 104-0045, Japan

About this study

power to detect a 50% increase in median TTF at 0.025 one-sided alpha in AC vs. D and AC vs. AC-D.

Results: 441pts (146 in AC, 147 in D, 148 in AC-D) were randomized between 01/99 and 05/03. Major grade 3-4 toxicities were neutropenia (26/45/46% for AC/D/AC-D), febrile neutropenia (3/4/6%), nausea/vomiting (3/3/4%). There was no toxic death. One grade 4 diarrhea in AC-D and 1 secondary leukemia (APL) in D were reported. Response (CR/PR) rates were 30, 41, and 35% for AC, D, and AC-D respectively. Median TTF (AC, D, and AC-D) are 6.4, 6.4, and 6.7 months (p =.255 for AC vs. D, p =.275 for AC vs. AC-D), and median overall survival are 22.4, 25.7, and 25.0 months (p=.092 for AC vs. D, p=.076 for AC vs. AC-D). The same difference was shown by the adjusted Cox model.

Conclusions: No benefit was demonstrated in D and AC-D over AC in TTF, however, D and AC-D tended to be superior to AC in response rate and overall survival. Survival benefit of front-line docetaxel should be re-evaluated by further long follow-up.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Hormonal therapy-resistant MBC
  • ER (-), failure of hormonal therapy for MBC, or relapse within 6 months after adjuvant hormonal therapy
  • No anthracyclines for MBC and no prior taxanes
  • At least 6 months from the completion of adjuvant chemotherapy
  • Measurable or evaluable lesions
  • Age: 20 to 75 years
  • PS: 0-3
  • WBC >= 4,000 /mm3 or ANC >=1,000 /mm3, Platelet >= 100,000 /mm3, SGOT/SGPT <= 1.5 x ULN, T-Bil <= 1.5 mg/dL, Cr <= 1.5 mg/dL
  • normal ECG
  • Written informed consent

Exclusion criteria

  • pregnant
  • malignant pleural effusion, ascites, or pericardial effusion that requires emergent treatment
  • Active infection
  • other cancer present within the last 5 years
  • previous stem cell transplantation
  • brain metastasis that requires emergent treatment
  • relapse within 6 months after completion anthracycline or during anthracycline
  • more than 250mg/m2 of anthracyclines
  • hypersensitivity of drug
  • interstitial pneumonitis or pulmonary fibrosis
  • positive HBs
  • antipsychotic medication
  • doctor's judgement

Treatment and study plan

AC (ADM 40mg/m2+CPA 500mg/m2) q21 days x 6 cycles

Drug

Docetaxel 60mg/m2 every 21 days for 6 cycles

Drug

AC and Docetaxel 60mg/m2 alternately q21 days for 6 cycles

Drug

Primary outcomes

  1. time to treatment failure

Secondary outcomes

  1. overall survival

  2. progression-free survival

  3. response rate

  4. adverse events

Sponsors and collaborators

Lead sponsor

Japan Clinical Oncology Group

Other

Collaborators

  • Ministry of Health, Labour and Welfare, Japan

Registry information

Official study title

Phase III Trial of Doxorubicin /Cyclophosphamide (AC), Docetaxel (D), and Alternating AC and D (AC-D) as Front-line Chemotherapy for Metastatic Breast Cancer: Japan Clinical Oncology Group Trial (JCOG9802)

Important dates

Study start
1999
Primary completion
2006
Study completion
2006
First posted
Sep 19, 2005
Registry last updated
Sep 2, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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