Background: OVA-301 is a large randomized trial that showed superiority of trabectedin plus pegylated liposomal doxorubicin (PLD; CentoCor Ortho Biotech Products L.P., Raritan, NJ, USA). over single-agent PLD in 672 patients with relapsed ovarian cancer, particularly in the partially platinum-sensitive subgroup [platinum-free interval (PFI) of 6-12 months]. This superiority has been suggested to be due to the differential impact of subsequent (platinum) therapy.

Patients And Methods: a detailed analysis of subsequent therapies and survival outcomes in the overall population and in the subsets according to platinum sensitivity was therefore conducted.

Results: similar proportions of patients received subsequent therapy in each arm (76% versus 77%), including further platinum-based regimens (49% versus 55%). Patients in the trabectedin/PLD arm received subsequent chemotherapy at a later time (median delay 2.5 months versus PLD arm). Overall survival from subsequent platinum was significantly prolonged in the partially platinum-sensitive disease subset (hazard ratio = 0.63; P = 0.0357).

Conclusion: the superiority of trabectedin/PLD over single-agent PLD in OVA-301 cannot be explained by differences in the extent or nature of subsequent therapies administered to these patients. On the other hand, these exploratory analyses support the hypothesis that the enhanced survival benefits in the partially platinum-sensitive subset might be due to an extended PFI leading to longer survival with subsequent platinum.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3003617PMC
http://dx.doi.org/10.1093/annonc/mdq353DOI Listing

Publication Analysis

Top Keywords

partially platinum-sensitive
12
subsequent platinum
12
trabectedin pegylated
8
pegylated liposomal
8
liposomal doxorubicin
8
relapsed ovarian
8
ovarian cancer
8
single-agent pld
8
subsequent therapies
8
received subsequent
8

Similar Publications

Background: This study aimed to evaluate the efficacy and safety of pegylated liposomal doxorubicin (PLD) for patients with partially platinum-sensitive, platinum-resistant, or platinum-refractory ovarian cancer.

Methods: Patients with partially platinum-sensitive, platinum-resistant, or platinum-refractory ovarian cancer were recruited in this prospective, open-label, single-arm, multicenter study. Eligible patients were given 4-6 cycles of PLD (40 mg/m2 on day 1, every 4 weeks).

View Article and Find Full Text PDF

Olaparib not cost-effective as maintenance therapy for platinum-sensitive, BRCA1/2 germline-mutated metastatic pancreatic cancer.

PLoS One

April 2024

Department of Public Health and Head of Research, Health Economics Facility, Institute of Pharmaceutical Medicine (ECPM), University of Basel, Basel, Switzerland.

Objective: To assess the cost-effectiveness and budget impact of olaparib as a maintenance therapy in platinum-responsive, metastatic pancreatic cancer patients harboring a germline BRCA1/2 mutation, using the Swiss context as a model.

Methods: Based on data from the POLO trial, published literature and local cost data, we developed a partitioned survival model of olaparib maintenance including full costs for BRCA1/2 germline testing compared to FOLFIRI maintenance chemotherapy and watch-and-wait. We calculated the incremental cost-effectiveness ratio (ICER) for the base case and several scenario analyses and estimated 5-year budget impact.

View Article and Find Full Text PDF

Objective: This study was designed to investigate the relationship between the Gustave-Roussy immune score (GRIm-score) and platinum resistance in patients with advanced high-grade serous ovarian cancer (HGSOC).

Methods: We conducted a retrospective study of patients diagnosed with advanced HGSOC between January 2017 and December 2020. A nomogram was developed to predict the risk of platinum resistance.

View Article and Find Full Text PDF
Article Synopsis
  • The study focuses on finding the optimal treatment for platinum-sensitive recurrent ovarian cancer (PSROC) by conducting a systematic review and a Bayesian network meta-analysis of available clinical trials up to March 2022.
  • It includes findings from 26 trials with a total of 10,441 patients and measures important outcomes like progression-free survival (PFS), overall survival (OS), and adverse events.
  • Results indicate that carboplatin-based combinations, specifically with pegylated liposomal doxorubicin and bevacizumab, show the greatest PFS, while other combinations provide significant survival benefits and lower treatment discontinuation rates.
View Article and Find Full Text PDF

Potential Targeted Therapies in Ovarian Cancer.

Pharmaceuticals (Basel)

October 2022

Molecular Unit, Department of Pathology, Herlev Hospital, University of Copenhagen, DK-2730 Herlev, Denmark.

Article Synopsis
  • The study focused on identifying genetic mutations in Danish patients with high-grade serous ovarian cancer (HGSC) to explore potential targeted therapies.
  • A total of 128 patients were analyzed, revealing varying sensitivity to platinum-based chemotherapy, with 21% having known druggable mutations for treatments like PARP inhibitors and other targeted therapies.
  • The results indicate that while PARP inhibitors are a prominent option, there are additional targeted therapies worth exploring based on the identified mutations.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!