ABSTRACT
This paper documents the results from the highly successful Lunar flashlight Optical Navigation Experiment with a Star tracker (LONEStar). Launched in December 2022, Lunar Flashlight (LF) was a NASA-funded technology demonstration mission. After a propulsion system anomaly prevented capture in lunar orbit, LF was ejected from the Earth-Moon system and into heliocentric space. NASA subsequently transferred ownership of LF to Georgia Tech to conduct an unfunded extended mission to demonstrate further advanced technology objectives, including LONEStar. From August to December 2023, the LONEStar team performed on-orbit calibration of the optical instrument and a number of different OPNAV experiments. This campaign included the processing of nearly 400 images of star fields, Earth and Moon, and four other planets (Mercury, Mars, Jupiter, and Saturn). LONEStar provided the first on-orbit demonstrations of heliocentric navigation using only optical observations of planets. Of special note is the successful in-flight demonstration of (1) instantaneous triangulation with simultaneous sightings of two planets with the LOST algorithm and (2) dynamic triangulation with sequential sightings of multiple planets.
ABSTRACT
OBJECTIVE: To review the efficacy and safety of niraparib for the treatment of recurrent epithelial ovarian, fallopian tube, and primary peritoneal cancer (OC, FTC, and PPC). DATA SOURCES: A literature search via MEDLINE through PubMed from August 2013 to January 2020 was performed using the key terms niraparib, PARP inhibitors, ovarian cancer, fallopian tube cancer, and primary peritoneal cancer. STUDY SELECTION AND DATA EXTRACTION: Completed and ongoing trials were identified through a review of the website trial registry https://www.clinicaltrials.gov. DATA SYNTHESIS: In a phase III, double-blind clinical trial, progression-free survival improved in patients treated with niraparib compared with placebo as maintenance treatment for patients with platinum-sensitive, recurrent OC: 21 versus 5.5 months in the germline breast cancer susceptibility gene (gBRCA) cohort (hazard ratio [HR] = 0.27; 95% CI = 0.17 to 0.41; P < 0.001) and 9.3 versus 3.9 months in the overall nongermline breast cancer susceptibility gene (non-gBRCA) cohort (HR = 0.45; 95% CI = 0.34 to 0.61; P < 0.001). Adverse events included thrombocytopenia and anemia. RELEVANCE TO PATIENT CARE AND CLINICAL PRACTICE: Poly (ADP-ribose) polymerase (PARP) inhibitors have gained a place in the therapeutic management of OC, FTC, and PPC because of their ability to suppress growth of homologous recombination deficiency-positive tumors, including those with BRCA1/2 mutations. Niraparib inhibits the DNA repair mechanism vital to the survival of cancer cells, poly-ADP ribose polymerase. CONCLUSIONS: PARP inhibitors can be used as a single agent for maintenance therapy for platinum-sensitive recurrent disease in patients with partial or complete response following 2 or more rounds of platinum-based therapy.
