Marilyn Mapp, DNP, RN, NEA-BC

Mapp

Dr. Mapp joined Cooper University Health Care in 2023. She provides operational oversight for the Women’s and Children’s Institute, including Obstetrics and Gynecology, Pediatrics, Child Life, Neonatal and Pediatric Critical Care, Cleft Palate Clinic, and the Safe Kids Outreach Program as well as Respiratory, Pulmonary Function Testing, and Interventional Pulmonary. 

Eileen F. Campbell, MSN, APN, FNP-BC

Campbell

Ms. Campbell is the Chief Advanced Practice Provider. Her administrative responsibilities include oversight and standardization of recruitment/retention, professional development and engagement, quality and safety, education and research activities for Advanced Practice Providers (APPs) and Licensed Independent Practitioners (LIPs). This broad oversight includes Nurse Practitioners, Physician Assistants, CRNAs and Psychologists. Ms.

Kathy Devine, DrNP, RN, NEA-BC

Kathleen Devine

Dr. Devine is responsible for professional nursing practice across the continuum of care to ensure safety, service, and quality outcomes for Cooper University Health Care's diverse patient population. In addition, she has administrative and operational leadership responsibility for Nursing and Patient Care Services. As SVP/CNE, Dr. Devine continues to advance nursing practice by engaging nurses in re-defining a professional practice model and shared governance structure that are grounded in theoretical tenets which align to organizational mission, vision, and values.

MDA 2023-0228 dMMR Phoenix

Submitted by rfreitag on

Short Title: Phoenix

To learn if cemiplimab can help to control dMMR colon cancer.

Study Number:

2023-0228

Study Status:

Enrolling

Treatment Agent:

Cemiplimab

Resources and Links

National Clinical Trial Identified Number: NCT05961709

Disease:

  • Colon

Study Phase:

II

researchcancer@cooperhealth.edu

Article Title

Phase II trial of cemiplimab for the non-operative management of localized dMMR colon cancer

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MDA 2016-0046 Exceptional Responders

Submitted by rfreitag on

Short Title: Exceptional Responders

This clinical trial studies eliminating surgery and how well radiation therapy after systemic therapy works in treating patients with HER2 positive or triple negative breast cancer when image-guided biopsy shows no residual cancer. Patients then receive standard breast radiotherapy.

Study Number:

2016-0046

Study Status:

Enrolling

Treatment Agent:

Radiation, Surgery

Resources and Links

National Clinical Trial Identified Number: NCT02945579

Disease:

  • Breast Cancer,
  • Estrogen Receptor Negative,
  • HER2 Positive Breast Carcinoma,
  • HER2/Neu Negative,
  • Invasive Breast Carcinoma,
  • Progesterone Receptor Negative,
  • Triple-Negative Breast Carcinoma,
  • Stage 1A, 1B, II, IIA, IIB

Study Phase:

Not applicable

researchcancer@cooperhealth.edu

Article Title

Multicenter trial for eliminating breast cancer surgery or radiotherapy in exceptional responders to neoadjuvant systemic therapy

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BR009

Submitted by rfreitag on

Short Title: BR009/OFSET

To determine whether adjuvant chemotherapy (ACT) added to ovarian function suppression (OFS) plus endocrine therapy (ET) is superior to OFS plus ET in improving invasive breast cancer-free survival (IBCFS) among premenopausal, early- stage breast cancer (EBC) patients with estrogen receptor (ER)-positive, HER2-negative tumors and 21-gene recurrence score (RS) between 16-25 (for pN0 patients) and 0-25 (for pN1 patients).

Study Number:

BR009

Study Status:

Enrolling

Treatment Agent:

Ovarian Function Suppression, Aromatase Inhibitor, Adjuvant Chemotherapy, Ovarian Function Suppression

Resources and Links

National Clinical Trial Identified Number: NCT05879926

Disease:

  • Breast Cancer

Study Phase:

III

ResearchCancer@CooperHealth.edu

Article Title

A Phase III Adjuvant Trial Evaluating the Addition of Adjuvant Chemotherapy to Ovarian Function Suppression plus Endocrine Therapy in Premenopausal Patients with pN0-1, ER-Positive/HER2-Negative Breast Cancer and an Oncotype Recurrence Score ≤ 25

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LU008

Submitted by rfreitag on

Short Title: LU008

This phase III trial compares the effect of adding stereotactic body radiation therapy (SBRT) to standard treatment (image guided radiation therapy [IGRT] and chemotherapy followed by immunotherapy with durvalumab) versus standard treatment alone in treating patients with non-small cell lung cancer that cannot be treated by surgery (inoperable). SBRT uses special equipment to position a patient and deliver radiation to tumors with high precision. This method may kill tumor cells with fewer doses over a shorter period and cause less damage to normal tissue. IGRT is a type of radiation that uses a computer to create picture of the tumor, to help guide the radiation beam during therapy, making it more accurate and causing less damage to healthy tissue.

Study Number:

LU008

Study Status:

Enrolling

Treatment Agent:

Cisplatin, Carboplatin, Paclitaxel, Pemetrexed, and Etoposide

Resources and Links

National Clinical Trial Identified Number: NCT05624996

Disease:

  • Locally Advanced Lung Non-Small Cell Carcinoma,
  • Stage IIB Lung Cancer AJCC v8,
  • Stage III Lung Cancer AJCC v8

Study Phase:

III

ResearchCancer@CooperHealth.edu

Article Title

Phase III Prospective Randomized Trial of Primary Lung Tumor Stereotactic Body Radiation Therapy Followed by Concurrent Mediastinal Chemoradiation for LocallyAdvanced Non-Small Cell Lung Canc

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