letrozole
Aliases
Femara
14 clinical trials
4 products
47 abstracts
22 indications
Indication
BRCA1 mutation carrierIndication
BRCA2 mutation carrierIndication
Breast CancerIndication
Hereditary Breast/Ovarian Cancer (BRCA1Indication
BRCA2Indication
HER2-positive breast cancerIndication
Breast cancerIndication
Breast cancer metastasisIndication
PainIndication
Joint painIndication
CapecitabineIndication
GastrinomaIndication
GlucagonomaIndication
InsulinomaIndication
Islet Cell CarcinomaIndication
Islet Cell TumorIndication
Recurrent Islet Cell CarcinomaIndication
somatostatinomaIndication
Gastroesophageal Junction AdenocarcinomaIndication
Gastric AdenocarcinomaClinical trial
Prevention of Breast Cancer by Letrozole in Post-menopausal Women Carrying a BRCA1/BRCA2 MutationStatus: Completed, Estimated PCD: 2019-06-01
Abstract
OPERA-01: A randomized, open-label, phase 3 study of palazestrant (OP-1250) vs standard-of-care for ER+, HER2- advanced or metastatic breast cancer patients after endocrine therapy and CDK4/6 inhibitors.Org: Gustave Roussy Cancer Center, Vall d’Hebron University Hospital/VHIO, Vall d’Hebron Institute of Oncology, Clinical Oncology Department, IRCCS Ospedale Policlinico San Martino Genoa, Genova, Italy, IRCCS Ospedale Policlinico San Martino Genoa,
Abstract
Nationwide real-world practice pattern and clinical data of palbociclib in patients with HR(+), HER2(-) metastatic breast cancer (KCSG BR21-15).Org: Division of Medical Oncology, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, South Korea, Department of Internal Medicine, Seoul National University Hospital, Seoul, Seoul, South Korea, Department of Internal Medicine, Seoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Seoul, South Korea, Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea, Division of Medical Oncology, Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea,
Abstract
First-in-human phase 1/2a study of the first-in-class, next-generation CDK4-selective inhibitor PF-07220060 + endocrine therapy (ET): Updated safety data in patients with HR+/HER2− mBC.Org: Centro Oncologico International,
Abstract
Addition of the MUC-1 vaccine tecemotide to neoadjuvant systemic therapy for patients with early breast cancer: Survival results from the prospective randomized ABCSG 34 trial.Org: Department of Obstetrics and Gynecology and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria, Austrian Breast and Colorectal Cancer Study Group, Wien, Austria, Department of Obstetrics and Gynecology and Comprehensive Cancer Center, Vienna, Austria, Department of Obstetrics and Gynecology, Medical University of Innsbruck, Innsbruck, Austria, Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria,
Abstract
A phase II trial comparing dalpiciclib in combination with letrozole versus standard chemotherapy as neoadjuvant therapy in patients with high-risk HR- positive HER-2 negative breast cancer: DARLING-02.Org: The Fourth Hospital of Hebei Medical University, Shijiazhuang, China, Breast Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China, Affiliated Hospital of Hebei Engineering University, Handan, China, First Hospital of Qinhuangdao, Qinhuangdao, China, Qinhuangdao Maternal and Child Health Hospital, Qinhuangdao, China,
Abstract
I-SPY2 Endocrine Optimization Pilot (EOP): Neoadjuvant amcenestrant +/- abemaciclib +/- letrozole in molecularly selected patients (pts) with HR+ HER2- stage 2/3 breast cancer (BC).Org: University of California, San Francisco, Mayo Clinic, University of Chicago Medical Center, Chicago, IL, Winship Cancer Institute of Emory University, Hunstman Cancer Institute at the University of Utah,
Abstract
Personalized neoadjuvant strategy in ER positive and HER2 negative breast cancer to increase BCS rate (PLATO): A prospective, multicenter, phase II clinical trial.Org: Seoul National University Hospital, Seoul National University College of Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul National University Bundang Hospital,
Abstract
LEONARDA-2: Lerociclib plus letrozole versus placebo plus letrozole in HR+/HER2- advanced or metastatic breast cancer.Org: Genor Biopharma Co.,Ltd., Genor Biopharma, Genor Biopharma Co.,Ltd., Shanghai, China, Genor Biopharma Co., Ltd., Beijing, China,
Abstract
Evaluating Ki67 and Oncotype DX Breast Recurrence Score during neoadjuvant treatment with letrozole/abemaciclib or chemotherapy in patients with highly proliferative HR+/HER2- breast cancer participating in the GEICAM CARABELA trial.Org: Spanish Breast Cancer Group, Málaga,
Abstract
Pharmacokinetics (PK) and pharmacogenomics (PGx) of ribociclib (ribo) in Black patients with metastatic breast cancer (mBC): The LEANORA study.Org: Georgetown University Medical Center, Washington, DC, Tufts Medical Center/Tufts University, Boston, MA, National Cancer Institute/National Institutes of Health,
Abstract
Surgical window of opportunity clinical trial of abemaciclib and letrozole for endometrioid adenocarcinoma of the endometrium.Org: Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Beijing, China, Northwestern Memorial Hospital, Chicago, IL, Chicago, IL, Il-Yang Pharmaceuticals, Northwestern University, Feinberg School of Medicine, Robert H. Lurie Comprehensive Cancer Center,
Abstract
Anlotinib plus hormone therapy in patients with platinum-resistant recurrent ovarian cancer: A prospective, single-arm, open-label, phase II study.Org: Xin Hua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Renji Hospital, Shanghai Jiaotong University School of Medicine,
Abstract
AFT-50 EndoMAP: A phase IB/II multicohort study of targeted agents and/or immunotherapy for patients with recurrent or persistent endometrial cancer (EC).Org: Weill Cornell Medicine and NewYork-Presbyterian Hospital, New York, NY, Alliance Statistics and Data Management Center, Mayo Clinic Rochester, Rochester, MN, University of Chicago Medicine, UCSF Helen Diller Family Comprehensive Cancer Center,
Abstract
Neoadjuvant aromatase inhibitor therapy for ER+ breast cancer: The NAOMI trial.Org: Dartmouth-Hitchcock Medical Center, Dartmouth College Geisel School of Medicine, Medical College of Wisconsin,
Abstract
A phase 2, open-label, single-arm, prospective, multicenter study of nab-sirolimus plus letrozole in advanced or recurrent endometrioid endometrial cancer.Org: Winthrop P. Rockefeller Cancer Institute, Women's Cancer Center of Nevada,
Abstract
Baseline (BL) characteristics and efficacy endpoints for patients (pts) with node-negative (N0) HR+/HER2− early breast cancer (EBC): NATALEE trial.Org: UCLA Santa Monica Hematology/Oncology Regulatory-2, Novartis Healthcare Private Limited, Novartis Ireland,
Abstract
Cost-effectiveness of adjuvant abemaciclib and ribociclib in high-risk, hormone receptor–positive, early breast cancer in India.Org: Department of Medical Oncology, BRA-IRCH,
Abstract
GOG 3088: A randomized phase II study of letrozole versus observation in patients with newly diagnosed uterine leiomyosarcoma.Org: Gynecologic Oncology Group Statistical and Data Center, Mount Pleasant, SC, Texas Oncology and Gynecologic Oncology Group (GOG) Foundation, Shenandoah, TX, GOG and Gynecologic Oncology,
Abstract
Neoadjuvant dalpiciclib combined with aromatase inhibitors in stage I-III HER2 negative luminal B breast cancer (DANCER): Preliminary findings from an ongoing phase II study.Org: Genecast Precision Medical Diagnostic Laboratory, Wuxi Co., Ltd, Wuxi, China,
Abstract
Aromatase inhibitor musculoskeletal toxicity (AIMT) in patients (pts) with early breast cancer (EBC): Prevalence, management, and association with non-adherence to AI.Org: Cancer Survivorship Program, INSERM 981, Gustave Roussy, Villejuif, France, INSERM 981, Gustave Roussy Département d'Organisation du Parcours Patient, Villejuif, France, France,
Abstract
Linking the companion diagnostic function of cancer genome profiling to therapy: Investigation of TMB-high predictors.Org: Hiroshima Prefectural Hospital, Hiroshima City North Medical Center Asa Citizens Hospital, JA Onomichi General Hospital, JA Hiroshima General Hospital,
Abstract
The impact of cannabidiol (CBD) on aromatase inhibitor (AI)-associated musculoskeletal symptoms (AIMSS).Org: University of Michigan Health Management Research Center,
Clinical trial
A Randomized, Open Label, Phase III Trial to Evaluate the Efficacy and Safety of Palbociclib + Anti-HER2 Therapy + Endocrine Therapy vs. Anti-HER2 Therapy + Endocrine Therapy After Induction Treatment for Hormone Receptor Positive (HR+)/HER2-Positive Metastatic Breast CancerStatus: Active (not recruiting), Estimated PCD: 2024-04-30
Clinical trial
Effect of Aromatase Inhibitor Therapy for Breast Cancer on Endothelial FunctionStatus: Completed, Estimated PCD: 2013-06-13
Clinical trial
Phase III Randomized, Placebo-Controlled Clinical Trial Evaluating the Use of Adjuvant Endocrine Therapy +/- One Year of Everolimus in Patients With High-Risk, Hormone Receptor-Positive and HER2/Neu Negative Breast CancerStatus: Active (not recruiting), Estimated PCD: 2022-12-01
Clinical trial
A Double Blind Randomization to Letrozole or Placebo for Women Previously Diagnosed With Primary Breast Cancer Completing Five Years of Adjuvant Aromatase Inhibitor Either as Initial Therapy or After Tamoxifen (Including Those in The MA.17 Study)Status: Completed, Estimated PCD: 2015-12-21
Clinical trial
Phase III Randomized Study of the Effects on Bone Mineral Density of Tamoxifen, Letrozole, and Letrozole + Zoledronic Acid as Adjuvant Treatment of Patients With Early Breast Cancer; VERSION 2 AMENDED Phase 3 Study of Triptorelin and Tamoxifen, Letrozole, or Letrozole + Zoledronic Acid in Adjuvant Treatment of Premenopausal Endocrine Responsive Breast Cancer Patients.Status: Active (not recruiting), Estimated PCD: 2024-11-01
Clinical trial
Aromatase Inhibitors Plus Metronomic Capecitabine in Treatment of Patients With Recurrent or Metastatic Hormone Receptor Positive, HER2 Negative Breast CancerStatus: Not yet recruiting, Estimated PCD: 2024-08-01
Clinical trial
Prospective Pilot Study to Determine the Effect of Aromatase Inhibitor-induced Estrogen Depletion on Evoked Pain Threshold and Psychosocial Factors in Breast Cancer PatientsStatus: Completed, Estimated PCD: 2012-07-01
Clinical trial
A Prospective, Phase II Trial Using ctDNA to Initiate Post-operation Boost Therapy After Adjuvant Chemotherapy in TNBC (Artemis)Status: Recruiting, Estimated PCD: 2028-09-01
Clinical trial
Clinical Effect Analysis of Different Regimens of Capecitabine in the Treatment of Patients With Advanced Colon CancerStatus: Completed, Estimated PCD: 2023-12-31
Clinical trial
A Randomized Phase II Study of Temozolomide or Temozolomide and Capecitabine in Patients With Advanced Pancreatic Neuroendocrine TumorsStatus: Active (not recruiting), Estimated PCD: 2021-05-26
Clinical trial
A Phase 3, Global, Multi-Center, Double-Blind, Randomized, Efficacy Study of Zolbetuximab (IMAB362) Plus CAPOX Compared With Placebo Plus CAPOX as First-line Treatment of Subjects With Claudin (CLDN) 18.2-Positive, HER2-Negative, Locally Advanced Unresectable or Metastatic Gastric or Gastroesophageal Junction (GEJ) AdenocarcinomaStatus: Active (not recruiting), Estimated PCD: 2022-10-25
Abstract
First-in-human first-in-class phase 1/2a study of the next generation CDK4-selective inhibitor PF-07220060 in patients (pts) with advanced solid tumors, enriched for HR+ HER2- mBC who progressed on prior CDK4/6 inhibitors and endocrine therapy.Org: Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Dana-Farber Cancer Institute, Sarah Cannon Research Institute/Tennessee Oncology, Yale Cancer Center, Yale School of Medicine, New Haven, CT, Pfizer, Inc.,
Abstract
Ribociclib and endocrine therapy as adjuvant treatment in patients with HR+/HER2− early breast cancer: Primary results from the phase III NATALEE trial.Org: David Geffen School of Medicine at University of California Los Angeles, Moscow City Oncology Hospital No.62, Sarah Cannon Research Institute/Tennessee Oncology, Tennessee Oncology, PLLC, National Taiwan University Hospital,
Abstract
Second-line endocrine therapy (ET) with or without palbociclib (P) maintenance in patients (pts) with hormone receptor-positive (HR[+])/human epidermal growth factor receptor 2-negative (HER2[-]) advanced breast cancer (ABC): PALMIRA trial.Org: Kent Oncology Centre, Istituto Europeo Oncologico, Hôpital Européen Georges Pompidou, Medica Scientia Innovation Research (MEDSIR), Pangaea Oncology,
Abstract
A phase II trial of palbociclib combined to letrozole after progression on second-line chemotherapy for women with ER/PR-positive high-grade serous or endometrioid ovarian, fallopian tube, or peritoneal cancer: LACOG 1018.Org: Hospital São Lucas da PUCRS, Hospital Fêmina - Grupo Hospitalar Conceição, Brazilian Gynecologic Oncology Group (EVA), Latin American Cooperative Oncology Group (LACOG), Division of Clinical Research and Technological Development - Brazilian National Cancer Institute (INCA),
Abstract
Evolving adjuvant estrogen therapy prescribing among breast oncology workforce.Org: University of Chicago, University of Chicago Medical Center, Chicago, IL, Section of Urology, Department of Surgery, Brigham and Women's Hospital, Boston, MA, University of Chicago Department of Urology,
Abstract
Alpelisib + endocrine therapy in patients with PIK3CA-mutated, hormone receptor–positive, human epidermal growth factor receptor 2–negative, advanced breast cancer: Analysis of all 3 cohorts of the BYLieve study.Org: University Hospitals, Leuven, Belgium, Medical Oncology Department, Hospital 12 de Octubre, Madrid, Spain, Institut Curie, PSL Research University, Saint-Cloud, France, Hospital Virgen del Rocio de Sevilla, Seville, Spain, Memorial Sloan Kettering Cancer Center, New York, NY, USA,
Abstract
PLEASURABLE: Results and biomarkers analysis from the phase II study of dalpiciclib combined with pyrotinib and endocrine therapy (ET) in women with dual-receptor positive (ER+/HER2+) metastatic breast cancer (MBC).Org: Fudan University Shanghai Cancer Center, Department of Breast Cancer, Hubei Cancer Hospital, Wuhan, China, Hubei Cancer Hospital, Tongji Medical College, Huazhong University of Science and Technology, Department of Breast Oncology, Peking University Cancer Hospital, Harbin Medical University Cancer Hospital,
Abstract
Disease-free survival (DFS) as a surrogate for overall survival (OS) in patients (pts) with HR+/HER2− early breast cancer (EBC): A correlation analysis.Org: Helios Klinikum Berlin-Buch, Dana-Farber Cancer Institute, International Breast Cancer Center, Quiron Group, Practice for Hematology and Internal Oncology, Latin American Cooperative Oncology Group (LACOG),
Abstract
Outcomes with first-line (1L) ribociclib (RIB) + endocrine therapy (ET) vs physician’s choice combination chemotherapy (combo CT) by age in pre/perimenopausal patients (pts) with aggressive HR+/HER2− advanced breast cancer (ABC): A subgroup analysis of the RIGHT Choice trial.Org: American University of Beirut Medical Center, National Cancer Centre of Singapore, Acıbadem Research Institute of Senology, Medical Oncology, Seoul National University Hospital, Independent Patient Advocate,
Abstract
Influence of ovarian function supression on quality of life in breast cancer survivors during adjuvant endocrine therapy.Org: School of Medicine University of Zagreb, Agency for Medicinal Products and Medical Devices of Croatia, University Hospital Centre Zagreb, General Hospital Sibenik, General Hospital Šibenik,
Abstract
ctDNA mutational profiles in luminal breast cancer with early vs late distant relapse: Geicam/2014-03.Org: Fundación Instituto Valenciano de Oncología (FIVO), GEICAM Spanish Breast Cancer Group, Valencia, Spain, GEICAM Spanish Breast Cancer Group, Barcelona, Spain, Hospital Universitario de Donostia-BioDonostia, Hospital de la Santa Creu i Sant Pau, Hospital Universitario de Canarias,
Abstract
lidERA Breast Cancer (BC): Phase III adjuvant study of giredestrant vs. physician’s choice of endocrine therapy (PCET) in patients (pts) with estrogen receptor-positive, HER2-negative early BC (ER+, HER2– eBC).Org: NSABP Foundation and UPMC Hillman Cancer Center, Pittsburgh, PA, Massachusetts General Hospital, Harvard Medical School, Boston, MA, Breast Center, Department of Obstetrics and Gynecology and CCC Munich, LMU University Hospital, Munich, Germany, Dan L. Duncan Comprehensive Cancer Center at Baylor College of Medicine, Houston, TX, University of California Los Angeles, Jonsson Comprehensive Cancer Center, Los Angeles, CA,
Abstract
AFT-50 EndoMAP: A phase IB/II multi-cohort study of targeted agents for patients with recurrent or persistent endometrial cancer.Org: Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN, University of Chicago, Chicago, IL,
Abstract
The effect of exercise on physical function and medication adherence in women receiving endocrine therapy for breast cancer: The Breast Cancer Endocrine Therapy Fitness (BE-FIT) randomized controlled trial.Org: University of British Columbia, BC Cancer Agency Vancouver Island Centre, British Columbia Cancer Agency, University of Toronto,
Abstract
Treatment patterns and clinical outcomes following endocrine resistance among with HER2-low metastatic breast cancer: Retrospective observational study.Org: Daiichi Sankyo Inc., Basking Ridge, NJ, NJ, Cardinal Health, Dublin, Ireland,
Abstract
Longitudinal trends in serum calcium, parathormone and bone mineral density in breast cancer survivors on aromatase inhibitor therapy: A single institutional cohort study.Org: Department of Internal Medicine C, University Hospital Greifswald, Greifswald, Germany, Cleveland Clinic Taussig Cancer Instititute, University of Pittsburgh Medical Center, Endocrinology and metabolic institute, Department of Hematology and Oncology, University Hospital Mannheim, Heidelberg University,
Abstract
Symptom burden of patients with breast cancer on adjuvant hormone therapy: A preliminary report.Org: Thomas Jefferson University, Sidney Kimmel Cancer Center at Thomas Jefferson University, Fox Chase Cancer Center,
Abstract
Neoadjuvant pyrotinib plus trastuzumab, dalpiciclib, and letrozole for triple-positive breast cancer: A pilot trial.Org: Jiangsu Hengrui Pharmaceuticals Co.,Ltd,
Abstract
Preliminary analysis of pyrotinib and dalpiciclib-based therapy in HER2-positive advanced breast cancer (ABC).Org: Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Science, Jinan, Shandong, China, Shandong University of Traditional Chinese Medicine Affiliated Hospital, Jinan, China, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital,Chinese Academy of Medical Science,Peking Union Medical College, Chinese Academy of Medical Sciences and Peking Union Medical College,
Abstract
CDK4/6 inhibitors and cardiovascular toxicity: Real-world evidence.Org: National and Kapodistrian University of Athens, Alexandra University Hospital,
Abstract
The real-world modeling of benefits demonstrated in major clinical trials on 2 HR+/HER2− metastatic breast cancer treatment with CDK4/6 inhibitor in the US: PALOMA-2 and MONALEESA-3.Org: University of Virginia Health System, Duke University Medical Center / Duke Cancer Institute, University of Virginia, Charlottesville, VA, USA,
Abstract
Feasibility of treatment with another CDK4/6 inhibitor after severe ribociclib liver toxicity.Org: EHC, Morges, Switzerland, University Hospital 12 de Octubre, Institut Curie, Saint Cloud, France, Centre GF Leclercq,
Abstract
First line combination of ribociclib and letrozole in patients (pts) with metastatic breast cancer (MBC): Focus on hepatic toxicity in the context of a real–world setting the Italian, multicenter Hermione–8 study.Org: Fondazione IRCCS San Gerardo dei Tintori, Clinical Cancer Centre, IRCCS-AUSL di Reggio Emilia, Ospedale Civile Guastalla, Hospital Piacenza,
Abstract
Malignancy in patients with sickle cell disease: A single center experience.Org: Louisiana State University Shreveport, Louisiana State University Health Sciences Center - Shreveport, LSU Health Shreveport, LSU Health Sciences Center, Louisiana State University (Shreveport) Program at Feist-Weiller Cancer Center, Shreveport, LA,
Product
Adjuvant endocrine therapyProduct
ribociclib and letrozoleProduct
Anlotinib + LetrozoleProduct
Letrozole + PalbociclibClinical trial
A Prospective, Randomized, Open-label, Multicenter Study Evaluating the Effects on Cognitive Functions of Adjuvant Endocrine Therapy in Postmenopausal Women With Breast Cancer.Status: Completed, Estimated PCD: 2012-04-04
Clinical trial
AN INTERVENTIONAL, OPEN-LABEL, RANDOMIZED, MULTICENTER, PHASE 2 STUDY OF PF-07220060 PLUS LETROZOLE COMPARED TO LETROZOLE ALONE IN POSTMENOPAUSAL WOMEN 18 YEARS OR OLDER WITH HORMONE RECEPTOR-POSITIVE, HER2-NEGATIVE BREAST CANCER IN THE NEOADJUVANT SETTINGStatus: Not yet recruiting, Estimated PCD: 2025-10-15