High-dose chemotherapy (CTM) for breast cancer
L E Damon1, J L Wolf, H S Rugo
1Division of Hematology/Oncology, The University of California, San Francisco 94143-0324, USA.
Bone Marrow Transplantation
|September 1, 2000
Summary
This study introduces a new high-dose chemotherapy regimen (CTM) for breast cancer, reducing pulmonary toxicity. The CTM regimen shows excellent outcomes for specific stages of breast cancer, with low treatment-related mortality.
Area of Science:
- Oncology
- Hematology
- Pharmacology
Background:
- Carmustine-based regimens for breast cancer can cause pulmonary injury.
- High-dose chemotherapy with autologous hematopoietic stem cell rescue is a treatment option for advanced breast cancer.
Purpose of the Study:
- To design and implement a novel mitoxantrone-based high-dose chemotherapy regimen (CTM) for breast cancer.
- To minimize pulmonary toxicity compared to carmustine-based regimens.
- To evaluate the efficacy and safety of the CTM regimen in various stages of breast cancer.
Main Methods:
- A cohort of 191 breast cancer patients received high-dose chemotherapy (cyclophosphamide, thiotepa, mitoxantrone) followed by stem cell rescue.
- Patients with Stage II/III disease also received radiation and tamoxifen (if applicable).
- Treatment-related mortality, pulmonary toxicity, cardiac events, and event-free survival (EFS) were assessed.
Main Results:
- The 5-year EFS for Stage II/IIIA patients with ≥10 positive lymph nodes was 62%.
- 5-year EFS rates were 44% for Stage IIIB and 17% for Stage IV breast cancer.
- Treatment-related mortality was 3%, with no delayed interstitial pneumonitis observed.
- Cardiac events were reduced after mitoxantrone dose adjustment.
Conclusions:
- The CTM regimen is associated with low treatment-related mortality and minimal pulmonary toxicity.
- CTM demonstrates excellent outcomes for Stage II/IIIA breast cancer patients with ≥10 involved axillary lymph nodes.
- Further investigation into mitoxantrone dose adjustment for cardiac safety is warranted.
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