Most Viewed Abstracts
1. Report Shows Shift in Starting Salaries for Physicians 2. Recommendations on the use of 18F-FDG PET in oncology 3. Taxane-based combinations as adjuvant chemotherapy of early breast cancer: a meta-analysis of randomized trials 4. Gene expression signatures, clinicopathological features, and individualized therapy in breast cancer 5. Sentinel node biopsy is important in mastectomy for ductal carcinoma in situ
Top Ten Searches
brca1 prostate-specific antigen sclc fobt egd bmi dysplasia hematologic ovarian hccYour Article Summary
Feasibility and efficacy of preoperative chemotherapy with docetaxel, cisplatin and S-1 in gastric cancer patients with para-aortic lymph node metastases
Anti-Cancer Drugs, 07/28/09
Fushida S et al. - In a trial to determine the maximum tolerated dose (MTD) and the dose-limiting toxicities as well as to evaluate the feasibility of chemotherapy with combined docetaxel, cisplatin, and S-1 (DCS therapy) in a preoperative setting, and also examine the pathological response, it was reported that preoperative DCS therapy was considered feasible and provided a high pathological response rate in gastric cancer pts with para-aortic lymph node metastases.
Methods- 15 pts received intravenous docetaxel and cisplatin (30, 35 or 40 mg/m2, each dose escalation was reciprocal) on days 1 and 15 and oral S-1 (40 mg/m2 twice daily) on days 1-14 every 4 wks.
- After 1 cycle of chemotherapy, toxicities were evaluated and after 2 cycles of chemotherapy, pts who were judged to be candidates for curative resection underwent gastrectomy with D2 lymphadenectomy plus para-aortic lymph node dissection.
- MTD was presumed to be at dose level 3 (docetaxel 40 mg/m2 and cisplatin 35 mg/m2).
- Dose-limiting toxicities were grade 4 neutropenia in 1 pt, grade 3 febrile neutropenia in 2 pts, and grade 3 diarrhoea in 2 pts.
- 13 of 15 pts received complete resection and there was no operation-related death.
- Good pathological responses were observed in 12 cases with lesions in the lymph nodes (complete response, n=4; partial response, n=8) and 11 pts with primary stomach lesions (complete response, n=2; partial response, n=9).
Today in GI Oncology...keeping you current
Receive free subspecialty "5-minute updates" via email
Randomized phase II study of gemcitabine administered at a fixed dose rate or in combination with cisplatin, docetaxel, or irinotecan in patients with metastatic pancreatic cancer
Journal of Clinical Oncology, 11/02/09
Dose finding and early efficacy study of gemcitabine plus capecitabine in combination with bevacizumab plus erlotinib in advanced pancreatic cancer
Journal of Clinical Oncology, 11/03/09
Chemoradiotherapy with concurrent gemcitabine and cisplatin with or without sequential chemotherapy with gemcitabine/cisplatin vs chemoradiotherapy with concurrent 5-fluorouracil in patients with locally advanced pancreatic cancer – a multi-centre randomised phase II study
British Journal of Cancer, 11/18/09
Sponsor
Article Search
Sponsor
Sponsor


See Latest Articles


