Intraperitoneal Alpha-emitting Radio Immunotherapy with Astatine-211 in Relapsed Ovarian Cancer; Long-term Follow-up with Individual Absorbed Dose Estimations

2019 ◽  
Vol 50 (4) ◽  
pp. S94
Author(s):  
Andreas Hallqvist ◽  
Per Albertsson ◽  
Ragnar Hultborn ◽  
Stig Palm ◽  
Karin Bergmark ◽  
...  
2019 ◽  
Vol 60 (8) ◽  
pp. 1073-1079 ◽  
Author(s):  
Andreas Hallqvist ◽  
Karin Bergmark ◽  
Tom Bäck ◽  
Håkan Andersson ◽  
Pernilla Dahm-Kähler ◽  
...  

2019 ◽  
Vol 50 (1) ◽  
pp. S24-S25 ◽  
Author(s):  
Andreas Hallqvist ◽  
Per Albertsson ◽  
Ragnar Hultborn ◽  
Stig Palm ◽  
Karin Bergmark ◽  
...  

2003 ◽  
Vol 91 (3) ◽  
pp. 563-568 ◽  
Author(s):  
Sean C Dowdy ◽  
Costas L Constantinou ◽  
Lynn C Hartmann ◽  
Gary L Keeney ◽  
Vera J Suman ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
K. N Srinivasan ◽  
Amit Rauthan ◽  
R. Gopal

Background. Ovarian cancer is the ninth most common cancer among women and causes more deaths than any other type of female reproductive cancer. Albumin-bound paclitaxel is known to increase intratumoral concentration of the paclitaxel by a receptor-mediated transport process across the endothelial cell wall, thereby breaching the blood/tumor interface. We present below three cases in which nab-paclitaxel based chemotherapy has been used in different settings for patients with ovarian cancer.Case Presentation. In the first case nab-paclitaxel was used along with carboplatin in adjuvant setting, in the second case, nab-paclitaxel was used along with carboplatin and bevacizumab as second line chemotherapy in a relapsed ovarian cancer case, and the third case delineates the use of nab-paclitaxel along with cisplatin as third line chemotherapy.Conclusion. In all the three scenarios, patients tolerated the chemotherapy well, as well as responding well to nab-paclitaxel based chemotherapy. The patients are currently on long-term follow-up and have been having an uneventful postchemotherapy.


2007 ◽  
Vol 25 (18_suppl) ◽  
pp. 5509-5509 ◽  
Author(s):  
A. C. Swart

5509 Background: ICON1 and a meta-analysis of all relevant trials demonstrated an improvement in 5 year recurrence-free and overall survival (RFS and OS) for women with early-stage epithelial ovarian cancer (ES EOC) treated with adjuvant chemotherapy compared to no adjuvant chemotherapy. We aimed to determine if this initial benefit is maintained long-term and whether benefit is different with different risk groups of patients defined by stage, grade and histology. Method: 477 women with ES EOC were recruited from centres in Italy (271 women) UK (195) Switzerland (11) between August 1991 and January 2000. 5-year results were presented at ASCO 2001. Systematic long-term follow up was planned and completed in May 2006. Results: With a median follow-up of 9.2 years, 168 women have developed recurrent disease or died and 144 women have died. The Hazard Ratio (HR) for RFS of 0.70 in favour of adjuvant chemotherapy (95% CI 0.52–0.95 p= 0.023) translated into an improvement of 10-year absolute RFS of 10% from 57 to 67%. For OS, HR was 0.74 (95% CI 0.53–1.02 p= 0.066), a corresponding improvement in 10-year absolute OS of 8% from 64% to 72%. 26% of patients died from causes other than ovarian cancer. Stage I patients were grouped as low (Ia, grade 1), medium (Ia grade 2, Ib or Ic grade 1) and high risk (Ia, grade 3, Ib or IC grade 2 or 3, any clear cell). The test of interaction between risk groups and adjuvant treatment for RFS and OS was 0.055 and 0.13, respectively. The HR, 95%CI and p value are summarised in the table . Conclusions The long-term benefit of adjuvant treatment on RFS is confirmed. There is clear evidence that adjuvant chemotherapy reduces the risk of recurrence/death or death alone in high-risk patients but not in the low-risk group. [Table: see text] [Table: see text]


Hybridoma ◽  
1995 ◽  
Vol 14 (2) ◽  
pp. 191-197 ◽  
Author(s):  
B. DONNERSTAG ◽  
R.P. BAUM ◽  
J.B. OLTROGGE ◽  
K. HENZEL ◽  
L. TRÄGER ◽  
...  

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