Carboplatin/etoposide as first-line chemotherapy in advanced ovarian carcinoma: a pilot study

1991 ◽  
Vol 27 (5) ◽  
pp. 389-393 ◽  
Author(s):  
Wolfgang Eiermann ◽  
Wolf Achterrath ◽  
Luigi Lenaz ◽  
Hermann Hepp
2004 ◽  
Vol 22 (14_suppl) ◽  
pp. 5135-5135
Author(s):  
A. García-Velasco ◽  
S. Hernando ◽  
C. Mendiola ◽  
D. Castellano ◽  
A. Sánchez-Muñoz ◽  
...  

2006 ◽  
Vol 24 (18_suppl) ◽  
pp. 5060-5060 ◽  
Author(s):  
H. Tanabe ◽  
N. Katsumata ◽  
K. Matsumoto ◽  
S. Nishio ◽  
Y. Kato ◽  
...  

5060 Background: There have been few reports of the relationship between CA125 nadir and the prognosis in patients with advanced ovarian carcinoma (AOC) who achieve a complete clinical response by multivariate analysis. Methods: CA125 nadir and the prognosis after the initial therapy (debulking surgery + first line chemotherapy) were retrospectively investigated in patients (pts) who had AOC meeting the criteria below and received therapy at National Cancer Center Hospital, between 1998 and 2004. The eligibility criteria were: 1) histological diagnosis of mullerian carcinoma, 2) FIGO stages III and IV, 3) a combination of platinum and taxane was administered as the first line chemotherapy, and 4) achieved clinically defined complete response (CR) after the initial therapy (ie, no cancer-related symptoms; normal physical examination, computed tomography scan of the abdomen/pelvis and chest x-ray). The possibility of CA125 nadir being a prognostic factor was investigated in pts who met these criteria by multivariate analysis (age (<50 years or 50 years≤), stage (III or IV), histological type (serous adenocarcinoma (serous) or non-serous), residual tumor diameter (<2 cm or 2 cm≤) and CA125 nadir (<10 U/ml or 10 U/ml≤)) using the Cox regression model. Results: There were 84 pts with a median age of 55.5 years (26–74). The stage was III in 59 pts and IV in 25 pts, the histological type was serous in 71 pts and non-serous in 13pts, and the residual tumor diameter was <2 cm in 72 pts and >2 cm in 12 pts and the median of CA125 before the initial therapy was 535 U/ml (13–28190), the CA125 nadir was <10 U/ml in 54 pts and 10 U/ml≤ in 30 pts, respectively. Regarding the prognosis, the median progression free survival (PFS) was 19 months (6–82), and the median overall survival (OS) was 36.5 months (10–82). By multivariate analysis, the CA125 nadir was significantly associated with the prognosis (hazard ratio of PFS was 0.39 (95% CI, 0.21–0.71), hazard ratio of OS was 0.28 (95% CI, 0.11–0.72)). Conclusion: CA125 nadir is a prognostic factor in patients with AOC who achieved clinically defined CR after the initial therapy, when the cut-off value was set to 10 U/ml. CA125 nadir may be an important factor for identifying pts for whom maintenance chemotherapy is effective. [Table: see text]


2004 ◽  
Vol 22 (14_suppl) ◽  
pp. 5135-5135
Author(s):  
A. García-Velasco ◽  
S. Hernando ◽  
C. Mendiola ◽  
D. Castellano ◽  
A. Sánchez-Muñoz ◽  
...  

Cancer ◽  
1991 ◽  
Vol 67 (11) ◽  
pp. 2867-2871 ◽  
Author(s):  
Laurel A. King ◽  
Gordon O. Downey ◽  
Roger A. Potish ◽  
Leon L. Adcock ◽  
Linda F. Carson ◽  
...  

1988 ◽  
Vol 74 (2) ◽  
pp. 217-220 ◽  
Author(s):  
Pier Franco Conte ◽  
Milena Bruzzone ◽  
Silvana Chiara ◽  
Riccardo Rosso ◽  
Giuseppe Giaccone ◽  
...  

Eleven untreated patients with advanced ovarian cancer were studied for tolerance and response to combination treatment with fixed doses of adriamycin (45 mg/m2) and cyclophosphamide (600 mg/m2) + escalating doses of carboplatin. At the first dose level of carboplatin (200 mg/m2), toxicity was acceptable. With carboplatin at 300 mg/m2, severe hematologic toxicity was observed. The dose-limiting toxicity was leukopenia. Although carboplatin was administered without any hydration, no patient experienced renal toxicity. Eight objective responses were observed in 9 clinically evaluable patients. At second look surgery, 3 complete responses and 4 partial responses were documented. Polychemotherapy with JAC (carboplatin, 200 mg/m2, adriamycin, 45 mg/m2, and cyclophosphamide, 600 mg/m2) is administrable with acceptable toxicity.


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