Patricia A. Ganz

Patricia A. Ganz

University of California, Los Angeles

H-index: 151

North America-United States

Description

Patricia A. Ganz, With an exceptional h-index of 151 and a recent h-index of 85 (since 2020), a distinguished researcher at University of California, Los Angeles, specializes in the field of breast cancer, quality of life, quality of care, survivors, genetics.

Professor Information

University

University of California, Los Angeles

Position

Professor

Citations(all)

93038

Citations(since 2020)

28399

Cited By

75404

hIndex(all)

151

hIndex(since 2020)

85

i10Index(all)

556

i10Index(since 2020)

389

Email

University Profile Page

University of California, Los Angeles

Research & Interests List

breast cancer

quality of life

quality of care

survivors

genetics

Top articles of Patricia A. Ganz

Work Productivity Among Younger Breast Cancer Survivors: The Impact of Behavioral Interventions for Depression

ObjectivesThe Pathways to Wellness randomized controlled trial found that 2 behavioral interventions, mindfulness awareness practices and survivorship education, reduced depressive symptoms in younger breast cancer survivors (BCSs) compared with wait-list control. This secondary analysis examines whether the interventions led to reduced loss of work productivity among younger BCSs and whether such reductions were mediated by reductions in depressive symptoms.MethodsThe Work Productivity and Activity Impairment scale was used to measure work productivity loss at 4 assessment time points. Correlates of productivity loss at enrollment were examined using multivariable linear regression. Differences in change over time in productivity loss between each intervention group and control were assessed using linear mixed models. Reduced depressive symptoms were tested as a mediator of reduced …

Authors

Catherine M Crespi,Patricia A Ganz,Ann H Partridge,Antonio Wolff,Hadine Joffe,Michael R Irwin,Katie Thure,Laura Petersen,Ya-Chen Tina Shih,Julienne E Bower

Journal

Value in Health

Published Date

2024/3/1

History and current status of the survivorship care program at the University of California, Los Angeles Jonsson Comprehensive Cancer Center (UCLA JCCC)

As one of the first comprehensive cancer centers to receive a designation from the National Cancer Institute, the Jonsson Comprehensive Cancer Center at UCLA Health has served as a leader in survivorship research for three decades. A clinical survivorship program for childhood cancer survivors was established in the early 2000s as this became a standard of care in pediatric oncology. However, it was not until receipt of external funding and the establishment of a Survivorship Center of Excellence in 2006 that clinical services were expanded to include adult cancer survivors, as well as survivorship care delivery research in the community and at affiliated clinical sites. When this funding ended, there was limited institutional support for expansion of the program, and so the clinical programs did not develop further. Recently, there has been renewed interest in obtaining Commission on Cancer accreditation, and …

Authors

Eden R Brauer,Patricia A Ganz

Journal

Journal of Cancer Survivorship

Published Date

2024/1/6

Abstract GS02-07: Loco-Regional Irradiation in Patients with Biopsy-proven Axillary Node Involvement at Presentation Who Become Pathologically Node-negative After Neoadjuvant …

Background: The benefit of adjuvant regional nodal irradiation including the chest wall after mastectomy (CWI+RNI) and with whole breast irradiation (WBI+RNI) after breast conserving surgery (BCS) is well established in pts with pathologically positive axillary nodes (pN+). Pts who present with axillary node involvement (cN+), receive neoadjuvant chemotherapy (NC), and are found to be pathologically node-negative at surgery (ypN0), have lower loco-regional recurrence (LRR) rates compared to those who remain pathologically node-positive (ypN+). This phase III, randomized trial aimed to evaluate whether CWI+RNI after mastectomy or addition of RNI to WBI after BCS significantly improves invasive breast cancer recurrence-free interval (IBC-RFI) in cN+ pts found to be ypN0 after NC. Methods: Eligible pts had clinical cT1-3, N1, M0 invasive breast cancer (biopsy-proven N+ by FNA …

Authors

Eleftherios Mamounas,Hanna Bandos,Julia White,Thomas Julian,Atif Khan,Simona Shaitelman,Mylin Torres,Frank Vicini,Patricia Ganz,Susan McCloskey,Nilendu Gupta,X Allen Li,Peter Lucas,Nadeem Abu-Rustum,Saumil Gandhi,Rahul Tendulkar,Robert Coleman,Keiichi Fujiwara,Samantha Seaward,William Irvin,Kristin Higgins,Robert Mutter,Jean-Francois Boileau,Andrew Muskovitz,Reshma Jagsi,Anna Weiss,Curran Walter Jr,Norman Wolmark

Journal

Cancer Research

Published Date

2024/5/2

Type I interferons, inflammation, and fatigue in a longitudinal RNA study of women with breast cancer

BackgroundFatigue is a common side effect of cancer and its treatment and is thought to be driven in part by activation of the proinflammatory cytokine network. However, the cellular and molecular underpinnings of cancer-related fatigue (CRF) have not been determined, nor have immune pathways beyond inflammation been carefully investigated. The goal of this study was to examine the association between CRF and activation of canonical proinflammatory gene regulation pathways and Type I interferon (IFN) signaling pathways in breast cancer patients during and after treatment.MethodsWomen diagnosed with early-stage breast cancer (n = 181) completed assessments before and after treatment with radiation and/or chemotherapy and at 6, 12, and 18-month post-treatment follow-ups. Assessments included self-reported fatigue (Multidimensional Fatigue Symptom Inventory – Short Form) and expression of …

Authors

Julienne E Bower,Patricia A Ganz,Michael R Irwin,Catherine M Crespi,Laura Petersen,Arash Asher,Sara A Hurvitz,Steve W Cole

Journal

Brain, Behavior, and Immunity

Published Date

2024/2/5

Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk

Background Nineteen genomic regions have been associated with high-grade serous ovarian cancer (HGSOC). We used data from the Ovarian Cancer Association Consortium (OCAC), Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA), UK Biobank (UKBB), and FinnGen to identify novel HGSOC susceptibility loci and develop polygenic scores (PGS). Methods We analyzed >22 million variants for 398,238 women. Associations were assessed separately by consortium and meta-analysed. OCAC and CIMBA data were used to develop PGS which were trained on FinnGen data and validated in UKBB and BioBank Japan. Results Eight novel variants were associated with HGSOC risk. An interesting discovery biologically was finding that TP53 3'-UTR SNP rs78378222 was associated with HGSOC (per T allele relative risk (RR)=1.44, 95%CI:1.28-1.62, P=1.76x10-9). The optimal PGS included 64,518 variants and was associated with an odds ratio of 1.46 (95%CI:1.37-1.54) per standard deviation in the UKBB validation (AUROC curve=0.61, 95%CI:0.59-0.62). Conclusions This study represents the largest GWAS for HGSOC to date. The results highlight that improvements in imputation reference panels and increased sample sizes can identify HGSOC associated variants that previously went undetected, resulting in improved PGS. The use of updated PGS in cancer risk prediction algorithms will then improve personalized risk prediction for HGSOC.

Authors

Daniel R Barnes,Jonathan P Tyrer,Joe Dennis,Goska Leslie,Manjeet K Bolla,Michael Lush,Amber M Aeilts,Kristiina Aittomaki,Nadine Andrieu,Irene L Andrulis,Hoda Anton-Culver,Adalgeir Arason,Banu K Arun,Judith Balmaña,Elisa V Bandera,Rosa B Barkardottir,Lieke PV Berger,Amy Berrington de Gonzalez,Pascaline Berthet,Katarzyna Bialkowska,Line Bjorge,Amie M Blanco,Marinus J Blok,Kristie A Bobolis,Natalia V Bogdanova,James D Brenton,Henriett Butz,Saundra S Buys,Maria A Caligo,Ian Campbell,Carmen Castillo,Kathleen BM Claes,GEMO Study Collaborators,EMBRACE Collaborators,Sarah V Colonna,Linda S Cook,Mary B Daly,Agnieszka Dansonka-Mieszkowska,Miguel de la Hoya,Anna deFazio,Allison DePersia,Yuan Chun Ding,Susan M Domchek,Thilo Dork,Zakaria Einbeigi,Christoph Engel,D Gareth Evans,Lenka Foretova,Renee T Fortner,Florentia Fostira,Maria Cristina Foti,Eitan Friedman,Megan N Frone,Patricia A Ganz,Aleksandra Gentry-Maharaj,Gord Glendon,Andrew K Godwin,Anna Gonzalez-Neira,Mark H Greene,Jacek Gronwald,Aliana Guerrieri-Gonzaga,Ute Hamann,Thomas vO Hansen,Holly R Harris,Jan Hauke,Florian Heitz,Frans BL Hogervorst,Maartje J Hooning,John L Hopper,Chad D Huff,David G Huntsman,Evgeny N Imyanitov,kConFab Investigators,Louise Izatt,Anna Jakubowska,Paul A James,Ramunas Janavicius,Esther M John,Siddhartha Kar,Beth Y Karlan,Catherine J Kennedy,Lambertus ALM Kiemeney,Irene Konstantopoulou,Jolanta Kupryjanczyk,Yael Laitman,Ofer Lavie,Kate Lawrenson,Jenny Lester,Fabienne Lesueur,Carlos Lopez Pleguezuelos,Phuong L Mai,Siranoush Manoukian,Taymaa May,Iain A McNeish,Usha Menon,Roger L Milne,Francesmary Modugno,Jennifer M Mongiovi,Marco Montagna,Kirsten B Moysich,Susan L Neuhausen,Finn C Nielsen,Catherine Nogues,Edit Olah,Olufunmilayo I Olopade,Ana Osorio,Laura Papi,Harsh Pathak,Celeste L Pearce,Inge S Pedersen,Ana Peixoto,Tanja Pejovic,Pei-Chen Peng,Beth N Peshkin,Paolo Peterlongo,C Bethan Powell,Darya Prokofyeva,Miquel Angel Pujana,Paolo Radice,Muhammad U Rashid,Gad Rennert,George Richenberg,Dale P Sandler,Naoko Sasamoto,Veronica W Setiawan,Priyanka Sharma,Weiva Sieh,Christian F Singer,Katie Snape,Anna P Sokolenko,Penny Soucy,Melissa C Southey,Dominique Stoppa-Lyonnet,Rebecca Sutphen,Christian Sutter,Manuel R Teixeira,Kathryn L Terry,Liv Cecilie V Thomsen,Marc Tischkowitz,Amanda E Toland,Toon Van Gorp,Ana Vega,Digna R Velez Edwards,Penelope M Webb,Jeffrey N Weitzel,Nicolas Wentzensen,Alice S Whittemore,Stacey J Winham,Anna H Wu,Siddhartha Yadav

Journal

medRxiv

Published Date

2024

Abstract PO1-19-01: NRG-BR008: A Phase III Randomized Trial of Radiotherapy Optimization for Low-risk HER2-positive Breast Cancer (HERO)

Background: Breast radiotherapy (RT) is the standard of care for patients with early-stage breast cancer (BC) who undergo breast-conserving surgery (BCS). However, the magnitude of benefit of RT is less clear in BCS patients with low-risk disease who receive effective systemic therapy. Among patients with early-stage HER2-positive (HER2+) BC, 10-year locoregional recurrence has been reported as low as 1.5% following BCS, adjuvant chemotherapy and HER2-targeted therapy, and RT. Given these exceedingly favorable outcomes, with the addition of HER2-directed therapy, we seek to evaluate the feasibility of omitting RT among patients with early-stage HER2+ BC following BCS and appropriate systemic therapy. Methods: This is a phase III randomized trial for patients ≥40 years with early-stage, node-negative HER2+ (IHC/FISH) BC treated with BCS with negative margins and sentinel lymph node biopsy …

Authors

Lior Braunstein,Melissa Mitchell,Hanna Bandos,William Sikov,Atif Khan,Peter Chen,Patricia Ganz,Reshma Jagsi,Julia White,Reena Cecchini,Hyejoo Kang,Shannon Puhalla,Kelly Bolton,Eileen Connolly,Erica Stringer-Reasor,Kimberly Gergelis,Thomas Julian,Eleftherios Mamounas,Norman Wolmark

Journal

Cancer Research

Published Date

2024/5/2

Patient-Reported Outcomes in OlympiA: A Phase III, Randomized, Placebo-Controlled Trial of Adjuvant Olaparib in gBRCA1/2 Mutations and High-Risk Human …

PURPOSEThe OlympiA randomized phase III trial compared 1 year of olaparib (OL) or placebo (PL) as adjuvant therapy in patients with germline BRCA1/2, high-risk human epidermal growth factor receptor 2–negative early breast cancer after completing (neo)adjuvant chemotherapy ([N]ACT), surgery, and radiotherapy. The patient-reported outcome primary hypothesis was that OL-treated patients may experience greater fatigue during treatment.METHODSData were collected before random assignment, and at 6, 12, 18, and 24 months. The primary end point was fatigue, measured with the Functional Assessment of Chronic Illness Therapy-Fatigue scale. Secondary end points, assessed with the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire, Core 30 item, included nausea and vomiting (NV), diarrhea, and multiple functional domains. Scores were compared between …

Authors

Patricia A Ganz,Hanna Bandos,Tanja Španić,Sue Friedman,Volkmar Müller,Sherko Kuemmel,Suzette Delaloge,Etienne Brain,Masakazu Toi,Hideko Yamauchi,Eduardo-M de Dueñas,Anne Armstrong,Seock-Ah Im,Chuan-gui Song,Hong Zheng,Tomasz Sarosiek,Priyanka Sharma,Cuizhi Geng,Peifen Fu,Kerstin Rhiem,Heike Frauchiger-Heuer,Pauline Wimberger,Daphné t'Kint de Roodenbeke,Ning Liao,Annabel Goodwin,Camille Chakiba-Brugère,Michael Friedlander,Keun Seok Lee,Sylvie Giacchetti,Toshimi Takano,Fernando Henao-Carrasco,Shamsuddin Virani,Frances Valdes-Albini,Susan M Domchek,Charles Bane,Edward C McCarron,Monica Mita,Giovanna Rossi,Priya Rastogi,Anitra Fielding,Richard D Gelber,Elsemieke D Scheepers,David Cameron,Judy Garber,Charles E Geyer,Andrew NJ Tutt

Journal

Journal of Clinical Oncology

Published Date

2024/2

Abstract PO1-19-02: A phase III trial evaluating De-escalation of Breast Radiation (DEBRA) following breast-conserving surgery (BCS) of stage 1, HR+, HER2-, RS≤ 18 breast …

Background: Approximately 50% of newly diagnosed invasive breast cancers are stage 1, with the majority being ER/PR-positive, HER2-negative. Genomic assays such as the Oncotype DX® have identified patients (pts) with reduced risk of distant metastasis and without benefit from chemotherapy added to endocrine therapy, freeing them from excess toxicity. Genomic assays are also recognized as prognostic for in-breast recurrence (IBR) after BCS and could similarly allow de-escalation of adjuvant radiotherapy (RT). Reducing overtreatment is of interest to pts, providers, and payers. Methods: We hypothesize that BCS alone is non-inferior to BCS plus RT for in-breast recurrence and breast preservation in women intending endocrine therapy (ET) for stage 1 invasive breast cancer (ER &/or PR positive, HER2-negative with an Oncotype DX Recurrence Score [RS] of ≤18). Stratification is by age (< 60; ≥60 …

Authors

Julia White,Reena Cecchini,Eleanor Harris,Eleftherios Mamounas,Daniel Stover,Patricia Ganz,Reshma Jagsi,Stewart Anderson,Carmen Bergom,Valérie Théberge,Mahmoud El-Tamer,Richard Zellars,Dean Shumway,Guang-Pei Chen,Thomas Julian,Norman Wolmark

Journal

Cancer Research

Published Date

2024/5/2

Professor FAQs

What is Patricia A. Ganz's h-index at University of California, Los Angeles?

The h-index of Patricia A. Ganz has been 85 since 2020 and 151 in total.

What are Patricia A. Ganz's research interests?

The research interests of Patricia A. Ganz are: breast cancer, quality of life, quality of care, survivors, genetics

What is Patricia A. Ganz's total number of citations?

Patricia A. Ganz has 93,038 citations in total.

What are the co-authors of Patricia A. Ganz?

The co-authors of Patricia A. Ganz are Michael Phelps, Ron D. Hays, Irwin MR; Irwin M, Robert Elashoff, Cheryl L. Rock, PhD, RD, Mark S Litwin.

Co-Authors

H-index: 172
Michael Phelps

Michael Phelps

University of California, Los Angeles

H-index: 161
Ron D. Hays

Ron D. Hays

University of California, Los Angeles

H-index: 126
Irwin MR; Irwin M

Irwin MR; Irwin M

University of California, Los Angeles

H-index: 109
Robert Elashoff

Robert Elashoff

University of California, Los Angeles

H-index: 94
Cheryl L. Rock, PhD, RD

Cheryl L. Rock, PhD, RD

University of California, San Diego

H-index: 93
Mark S Litwin

Mark S Litwin

University of California, Los Angeles

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