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[High-dose chemotherapy and peripheral hemtopoietic cells (PBPC) in solid tumors]
G Rosti1, P Ferrante, A Tienghi
1Oncologia Medica Ravenna, Istituto Oncologico Romagnoto, Ravenna.
Tumori
|March 1, 1996
Summary
High-dose chemotherapy, including autologous bone marrow transplantation (ABMT) and peripheral blood progenitor cell transplantation (PBPCT), shows promise for solid tumors, especially breast cancer. This approach offers improved survival rates and reduced toxicity compared to standard treatments.
Area of Science:
- Oncology
- Hematology
- Cancer Therapeutics
Context:
- High-dose chemotherapy is increasingly utilized for solid tumors in Europe and North America.
- Autologous bone marrow transplantation (ABMT) and peripheral blood progenitor cell transplantation (PBPCT) are common procedures, particularly for breast carcinoma.
- Ongoing trials are evaluating the efficacy of high-dose chemotherapy in the adjuvant setting for high-risk breast cancer.
Purpose:
- To review the current status of high-dose chemotherapy for solid tumors.
- To discuss new technologies and their applications in high-dose chemotherapy.
- To highlight the benefits and challenges associated with ABMT and PBPCT.
Summary:
- Phase II trials indicate high-dose chemotherapy yields superior disease-free survival rates in high-risk breast cancer patients compared to standard doses.
- A trial in advanced disease favored high-dose cyclophosphamide, mitoxantrone, and etoposide over standard regimens, improving overall survival and time to relapse.
- The adoption of PBPCT over ABMT has improved tolerability and reduced costs, with a significant decrease in toxic death rates for breast cancer patients.
Impact:
- High-dose chemotherapy demonstrates significant potential in improving outcomes for patients with various solid tumors, including breast cancer and germ cell tumors.
- Reduced toxicity and cost-effectiveness associated with PBPCT enhance patient management.
- Further research is needed to address the debate surrounding PBPC contamination by tumor cells.