Matching articles for "Ovarian cancer"

Mirvetuximab Soravtansine (Elahere) for Ovarian, Fallopian Tube, and Primary Peritoneal Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • December 12, 2022;  (Issue 1665)
Mirvetuximab soravtansine-gynx (Elahere – Immuno-Gen), an antibody-drug conjugate, has received accelerated approval by the FDA for treatment of folate receptor (FR) alpha-positive,...
Mirvetuximab soravtansine-gynx (Elahere – Immuno-Gen), an antibody-drug conjugate, has received accelerated approval by the FDA for treatment of folate receptor (FR) alpha-positive, platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer in adults who received 1-3 prior lines of systemic therapy. Accelerated approval was based on the overall response rate and median duration of response.
Med Lett Drugs Ther. 2022 Dec 12;64(1665):e205-6 | Show Full IntroductionHide Full Introduction

PARP Inhibitors for Ovarian Cancer

   
The Medical Letter on Drugs and Therapeutics • December 4, 2017;  (Issue 1535)
Three oral poly(ADP-ribose) polymerase (PARP) inhibitors have been approved by the FDA for treatment of advanced, recurrent ovarian cancer. Olaparib (Lynparza – AstraZeneca), niraparib (Zejula –...
Three oral poly(ADP-ribose) polymerase (PARP) inhibitors have been approved by the FDA for treatment of advanced, recurrent ovarian cancer. Olaparib (Lynparza – AstraZeneca), niraparib (Zejula – Tesaro), and rucaparib (Rubraca – Clovis) are each approved for somewhat different indications and for patients with different biomarkers (see Table 2).
Med Lett Drugs Ther. 2017 Dec 4;59(1535):200-2 | Show Full IntroductionHide Full Introduction

Olaparib (Lynparza) for Advanced Ovarian Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • February 29, 2016;  (Issue 1489)
The FDA has approved the oral poly (ADP-ribose) polymerase (PARP) inhibitor olaparib (Lynparza – Astra-Zeneca) as monotherapy for treatment of women with advanced ovarian cancer who have BRCA1/2...
The FDA has approved the oral poly (ADP-ribose) polymerase (PARP) inhibitor olaparib (Lynparza – Astra-Zeneca) as monotherapy for treatment of women with advanced ovarian cancer who have BRCA1/2 germline mutations and have received at least 3 prior lines of chemotherapy. Olaparib is the first PARP inhibitor to be approved in the US. It is approved outside the US for maintenance treatment of relapsed BRCA-mutated ovarian cancer.
Med Lett Drugs Ther. 2016 Feb 29;58(1489):e32-3 | Show Full IntroductionHide Full Introduction

Cancer Screening

   
The Medical Letter on Drugs and Therapeutics • December 1, 2012;  (Issue 124)
Use of screening tests to identify cancers before they cause symptoms can lead to earlier therapy and may improve outcomes. Screening tests for some common cancers are reviewed...
Use of screening tests to identify cancers before they cause symptoms can lead to earlier therapy and may improve outcomes. Screening tests for some common cancers are reviewed below.
Treat Guidel Med Lett. 2012 Dec;10(124):87-94 | Show Full IntroductionHide Full Introduction

BRCA Screening

   
The Medical Letter on Drugs and Therapeutics • November 19, 2007;  (Issue 1274)
Direct-to-consumer advertisements are urging women to be tested for mutations in BRCA1 and BRCA2 genes, which are the most common known causes of an inherited predisposition to breast and ovarian cancer....
Direct-to-consumer advertisements are urging women to be tested for mutations in BRCA1 and BRCA2 genes, which are the most common known causes of an inherited predisposition to breast and ovarian cancer. Clinically important BRCA mutations have been found in about 2% of Ashkenazi Jewish women, and are estimated to occur in about 1 in 300 to 500 women in the general non-Jewish US population. The prevalence appears to be lower in non-whites.
Med Lett Drugs Ther. 2007 Nov 19;49(1274):93-4 | Show Full IntroductionHide Full Introduction

Topotecan Hydrochloride for Metastatic Ovarian Cancer

   
The Medical Letter on Drugs and Therapeutics • October 25, 1996;  (Issue 986)
Topotecan hydrochloride (Hycamtin - SmithKline Beecham) was recently approved by the U.S. Food and Drug Administration for parenteral use as a single agent in patients with metastatic ovarian cancer...
Topotecan hydrochloride (Hycamtin - SmithKline Beecham) was recently approved by the U.S. Food and Drug Administration for parenteral use as a single agent in patients with metastatic ovarian cancer refractory to other drugs. Initial treatment for metastatic ovarian cancer usually consists of cisplatin (Platinol) or carboplatin (Paraplatin) plus paclitaxel (Taxol) or cyclophosphamide (Cytoxan, and others).
Med Lett Drugs Ther. 1996 Oct 25;38(986):96-7 | Show Full IntroductionHide Full Introduction