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Evangeline A. Reyes, MD To provide quality healthcare to cancer patients comprised of compassion, dedication, and honesty. To maintain knowledge in and to provide patients with the most up-to-date medical care available. PROFESSIONAL EXPERIENCE 2002 – present Hematologist/Oncologist 2001 – 2002 Hematologist/Oncologist 2000 – 2001 Hematologist/Oncologist 1997 – 1999 Hematologist/Oncologist LEADERSHIP POSITIONS 1997 – 1999 Chair, Clinical Protocols, Blair Medical Associates/Altoona Hospital 1998 – 1999 Vice Chair, Altoona Hospital Institutional Review Board 1998 – 1999 Instructor: Hematology/Oncology, Allegheny Family Residency Program
HOSPITAL AFFILIATION APPOINTMENTS Fountain Valley Regional Hospital & Medical Center, Fountain Valley, California EDUCATION June 1984 – April 1988 Medical Degree RESIDENCY July 1991 – June 1994 Internship and Residency FELLOWSHIPS July 1994 – June 1997 Fellow, Hematology/Oncology BOARD CERTIFICATION Diplomate, Medical Oncology, November 1999 LICENSURE Virginia License #053406 RESEARCH AFFILIATIONS Member of National Surgical Adjuvant Breast and Bowel Project (NSABP) MEMBERSHIPS American Society of Clinical Oncology BIOGRAPHICAL DATA Date of Birth: January 7, 1962 CLINICAL RESEARCH ACTIVITY BLADDER CANCER Interleukin 2 in an Alternative Dose: Treatment of Patients with Metastatic Renal Cell Cancer with Low Dose Proleukin BREAST CANCER Randomized Trial of Gemcitabine Plus Docetaxel vs. Docetaxel Plus Capecitabine in Metastatic Breast Cancer in 1st and 2nd Line Patients An Open-Label, Randomized, Multicenter Study to Evaluate the Use of Zoledronic Acid in the Prevention of Cancer Treatment Related Bone Loss in Postmenopausal Women with ER+ and/or PR+ Breast Cancer Receiving Letrozole as Adjuvant Therapy A Double-Blind, Placebo-Controlled, Multicenter, Randomized Study Evaluating the Prophylactic Use of Pegfilgrastim on the Incidence of Febrile Neutropenia in Subjects with Advanced Breast Cancer Treated with Single Agent Docetaxel A Multicenter Phase III Randomized Trial Comparing Docetaxel In Combination With Doxorubicin And Cyclophosphamide (TAC) Versus Doxorubicin And Cyclophosphamide Followed By Docetaxel (AC⇐T) As Adjuvant Treatment Of Operable Breast Cancer HER2NEU Negative Patients With Positive Axillary Lymph Nodes BREAST CANCER CONTINUED A Multicenter Phase III Randomized Trial Comparing Doxorubicin and Cyclophosphamide Followed by Docetaxel (AC⇐T) with Doxorubicin and Cyclophosphamide Followed by Docetaxel and Trastuzumab (AC⇐TH) and with Docetaxel, Platinum Salt and Trastuzumab (TCH) in th Adjuvant Treatment of Node Positive and High Risk Node Negative Patients with Operable Breast Cancer Containing the HER2NEU Alteration A Multicenter Phase III Randomized Trial Comparing Docetaxel (Taxotere®) and Trastuzumab (Herceptin®) with Docetaxel (Taxotere®), Carboplatin, and Trastuzumab (Herceptin®) as First line Chemotherapy for Patients with Advanced Breast Cancer Containing the HER2Gene Amplification Phase III Study Of Epirubicin/Cyclophosphamide Followed By Taxane (Sequential Chemotherapy) Vs Epirubicin/Taxane (Concurrent Chemotherapy) As Adjuvant Treatment For Operable, Node-Positive Breast Cancer Breast Cancer Siblings Database Clinical Outcomes in Patients with HER2 Gene-Amplified Metastatic Breast Cancer Treated with First-Line Herceptin® in Combination with a Taxane: A Phase IV, Prospective, Community-Based Study The Traviota Study: Trastuzumab (Herceptin®) and Either Vinorelbine (Navelbine®) or Taxane-Based Chemotherapy in Patients with HER2 Overexpressing Metastatic Breast Cancer: A Randomized Phase III Study Study of Tamoxifen and Raloxifene (STAR) for the Prevention of Breast Cancer. Open-Label Study of Femara (2.5 mg) Daily for Patients with ER Receptor Positive Advanced Breast Cancer. BREAST CANCER CONTINUED A Randomized, Open-Label, Phase III Study of RPR109881 IV Every 3 Weeks Versus Capcitabine (Xeloda®) Tablets Twice Daily For 2 Weeks in 3-week Cycles in Patients With Metastatic Breast Cancer Progressing After Taxanes and Anthracycline therapy. A Randomized, Double Blind, Multicenter Study to Compare the Efficacy and Tolerability of fulvestrant (FASLODEX™) vs. exemestane (AROMASIN™) in Postmenopausal Women with Hormone Receptor Positive Advanced Breast Cancer with Disease Progression after Prior Non-Steroidal Aromatase Inhibitor (AI) Therapy COLORECTAL CANCER A Phase III, Multicenter, Randomized, Active-Controlled Clinical Trial to Evaluate the Efficacy and Safety of rhuMAb VEGF (Bevacizumab) in Combination with Standard Chemotherapy in Subjects with Metastatic Colorectal Cancer; Second-line Treatment of rhuMAb VEGF with or without Chemotherapy for Subjects whose Cancer Progressed on the Protocol An Open-Label Phase II Study of Intermittent Oral Capecitabine in Combination with Intravenous Irinotecan (Q3W) in Patients with Advanced and/or Metastatic Colorectal Cancer A Compassionate Use Study of Oxaliplatin in the Treatment of Metastatic Colorectal Carcinoma COLORECTAL CANCER CONTINUED An Open-Label, Single-Arm Trial of Patients with Metastatic Colorectal Cancer Receiving Irinotecan, 5-Fluorouracil, and Leucovorin Followed by Leukine, a Recombinant Human Granulocyte-Macrophage Colony Stimulating Factor (GM-CSF) A Treatment Access Program with Oxaliplatin for Previously Treated Colorectal Cancer An Open-Label Randomized Phase III Study Comparing Xeloda with IV Bolus 5-FU in Combination with Low Dose Leucovorin as Adjuvant Chemotherapy in Patients who Underwent Surgery for Dukes C Colon Cancer.
GASTRIC CANCER Open Label, Randomized Multicenter Phase II/III Study of Docetaxel in Combination with Cisplatin (CDDP) or Docetaxel in Combination with 5-FU and CDDP Compared to the Combination of CDDP and 5-FU in Patients with Metastatic or Locally Recurrent Gastric Cancer Previously Untreated with Chemotherapy for Advanced Disease. A Double-Blind, Randomized, Placebo-Controlled Study of the Efficacy and Safety of Epoetin Alfa Administered Weekly in Patients with Gastric or Rectal Cancers Undergoing Preoperative Chemoradiation Followed by Surgery HEMATOLOGIC MALIGNANCIES HEMATOLOGIC MALIGNANCIES CONTINUED A Multi-center, Open-Label Study Evaluating the Efficacy and Safety of Rituxan (Rituximab) in Combination with Six Cycles of Cyclophosphamide, Doxorubicin, Vincristine, Prednisone (CHOP) Followed by Rituxan Maintenance as Initial Therapy for Patients with Advanced Stage Indolent Non-Hodgkin’s Lymphoma LUNG CANCER An Open-Label, Multicenter, Non-Comparative Study of Topotecan as Single Agent. Second-Line Therapy (Administered Intravenously as Five Daily Doses Every 21 Days) in Patients With Small Cell Cancer. A Phase III, Randomized, Double-Blind, Multi-Center Study of the Efficacy of Taxotere in Combination with Aptosyn versus Taxotere and Placebo in NSCLC Patients after Failure of Prior Platinum-Based Chemotherapy An Open-Label, Multicenter, Randomized Phase III Study of Hycamtin Topotecan) as Single Agent, Second-Line Therapy (Administered Intravenously as Five Daily Doses Every 21 Days) Versus Second CAV In Patients With SCLC Who Have Relapsed at Least Three Months After Completion Of First-Line Therapy A Randomized, Phase III Trial Comparing CPT-11 (Irinotecan HCL; Camptosar Injection)/ Cisplatin with Etoposide / Cisplatin in Patients with Previously Untreated, Extensive, Small-Cell Lung Cancer LUNG CANCER CONTINUED An Expanded Access Clinical Program with ZD1839 (Iressa™) for Patients with Advanced Non-small Cell Lung Cancer (NSCLC) A Randomized, Open-Label, Parallel Group, International, Multicenter, Phase III Trial of Oral ZD1839 (IRESSA®) Versus Intravenous Docetaxel (Taxotere®) in Patients with Locally Advanced or Metastatic Recurrent Non-Small Cell Lung Cancer who have Previously Received Platinum-based Chemotherapy PANCREATIC CANCER A Double-Blind, Randomized, Mulit-center, Study of Orathecin Capsules Plus Gemcitabine Versus Placebo Capsules Plus Gemcitabine (With an Open-Label Single-Arm Pre-Randomization Phase) in Chemonaive Patients with Non-Resectable Pancreatic Cancer RENAL CANCER Open-Label, Non-comparative Treatment Protocol for the use of Sorafenib in Patients with Advanced Renal Cell Carcinoma. SUPPORTIVE THERAPY A Pilot Study to Evaluate the Response Rate of Procrit at 40,000 Units Once Weekly in Anemic Cancer Patients Not Receiving Chemotherapy A Randomized, Double-Blind, Placebo-Controlled Comparison of the Analgesic Activity of Valdecoxib 40 mg BID as Add On Therapy to Opioid Medication in Patients with Chronic Cancer Pain. SUPPORTIVE THERAPY CONTINUED A Randomized Dose-Finding Study of NESP Administered by SQ Injection for the Treatment of Anemia in Subjects with Solid Tumors Receiving Multicycle Chemotherapy A Double Blind, Efficacy and Safety Study of the Oral Direct Thrombin Inhibitor, H376/95 versus Standard Therapy in Patients with Active, Symptomatic DVT with or without PE. A Randomized, Open-Label, Multicenter Study of Subcutaneous and Intravenous Administration of Darbepoetin Alfa (Novel Erythropoiesis Stimulating Protein, NESP) for the Treatment of Anemia in Subjects with Non-Myeloid Malignacies Receiving Multicycle Chemotherapy Multicenter, Phase III, Open-Label, Uncontrolled Study to Assess the Safety and Efficacy of a Single Oral Dose of Palonosetron 0.75 mg in the Prevention of Chemotherapy Induced Nausea and Vomiting in Cancer Patients Undergoing Repeated Cycles of Moderately Emetogenic Chemotherapy A Multi-Center, Open-Label, Long-Term Study of OraVescent® Fentanyl Citrate for the Treatment of Breakthrough Pain in Opioid-Tolerant Cancer Patients A Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of ORAVESCENT® Fentanyl Citrate in Opioid-Tolerant Patients With Cancer and Breakthrough Pain |
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