Abstract | BACKGROUND: To evaluate the safety and efficacy of dose-dense weekly chemotherapy in the treatment of advanced thymoma. METHODS: RESULTS: From July 1997 to March 2004, 30 patients were entered. Three were ineligible due to different histology. Chemotherapy-associated toxicity was mainly haematological and was well tolerated, with no deaths due to toxicity, and 87% of patients completed the planned 9-week regimen. Overall response rate was 59%, with 16 of the 27 eligible patients achieving partial response. Median progression-fee survival (PFS) was 0.79 years (95% confidence interval: 0.52-1.40 years), and PFS at 1 and 2 years was 37 and 15%, respectively. Overall survival rates at 2 and 5 years were 89 and 65%, respectively. CONCLUSION: In stage-IV thymoma patients, weekly dose-dense chemotherapy offers similar activity to conventional regimens.
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Authors | H Kunitoh, T Tamura, T Shibata, K Nakagawa, K Takeda, Y Nishiwaki, Y Osaki, K Noda, A Yokoyama, N Saijo, JCOG Lung Cancer Study Group, Tokyo, Japan |
Journal | British journal of cancer
(Br J Cancer)
Vol. 101
Issue 9
Pg. 1549-54
(Nov 03 2009)
ISSN: 1532-1827 [Electronic] England |
PMID | 19809436
(Publication Type: Clinical Trial, Phase II, Journal Article, Research Support, Non-U.S. Gov't)
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Topics |
- Adolescent
- Adult
- Aged
- Antineoplastic Combined Chemotherapy Protocols
(adverse effects, therapeutic use)
- Dose-Response Relationship, Drug
- Female
- Humans
- Japan
- Male
- Middle Aged
- Neoplasm Staging
- Thymoma
(drug therapy, mortality, pathology)
- Thymus Neoplasms
(drug therapy, mortality, pathology)
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