Saturday, June 3, 2017, Chicago, IL — 7:00 PM – 9:30 PM (Central Time)

Cases from the Community: Clinical Investigators Provide Their Perspectives on Emerging Research and Actual Patients with Gastrointestinal Cancers

Location:
Hilton Chicago
720 South Michigan Avenue
Chicago, IL 60605
Hotel Phone: (312) 922-4400

Time:
6:30 PM – 7:00 PM (Central Time) — Registration and Dinner Buffet
7:00 PM – 9:30 PM (Central Time) — Educational Meeting

Meeting Room:
Grand Ballroom (Level 2)

There is no registration fee for this event. However, preregistration is advised as seating is limited.  
 
Faculty:
Gabriela Chiorean, MD
Associate Professor of Medicine
University of Washington School of Medicine
Seattle, Washington

Anthony El-Khoueiry, MD
Associate Professor of Clinical Medicine
Medical Director of
Clinical Investigations Support Office
Phase I program director
USC Norris Comprehensive Cancer Center
Los Angeles, California

Charles S Fuchs, MD, MPH
Director, Yale Cancer Center
Physician-in-Chief, Smilow Cancer Hospital
Richard and Jonathan Sackler
Professor of Internal Medicine
New Haven, Connecticut

Axel Grothey, MD
Professor of Oncology
Department of Medical Oncology
Mayo Clinic
Rochester, Minnesota


Michael J Overman, MD
Associate Professor
Department of Gastrointestinal (GI)
Medical Oncology
Division of Cancer Medicine
The University of Texas MD Anderson
Cancer Center
Houston, Texas

Eric Van Cutsem, MD, PhD
Professor of Medicine
Digestive Oncology
University Hospital Gasthuisberg/Leuven
Leuven, Belgium

Moderator:
Neil Love, MD
Research To Practice
Miami, Florida

Not an official event of the 2017 ASCO Annual Meeting. Not sponsored, endorsed, or accredited by ASCO or the Conquer Cancer Foundation.

The agenda for this unique meeting has been designed to provide practical perspectives on current and emerging treatment strategies. Each module will feature discussion of cases submitted on video by practicing general oncologists followed by a faculty presentation reviewing relevant data sets and promising investigational approaches.

MODULE 1: Biomarker Assessment and Selection of Therapy for Patients with Newly Diagnosed Metastatic Colorectal Cancer (mCRC) — Dr Grothey

Topics to be reviewed during case discussion and faculty presentation

  • Effect of primary tumor sidedness on prognosis and systemic treatment decision-making
  • Role of tissue testing, including RAS, BRAF and microsatellite instability (MSI)
  • Prevalence and prognostic significance of various BRAF mutations among patients with advanced CRC; effects, if any, of a BRAF V600E mutation on current nonresearch decision-making
  • Frequency of HER2 amplification in patients with mCRC; indications for HER2 testing and nonresearch role of anti-HER2 therapy
  • Considerations for systemic perioperative therapy in patients with oligometastatic disease

MODULE 2: Clinical and Palliative Care Considerations for Patients with Progressive mCRC — Prof Van Cutsem

Topics to be reviewed during case discussion and faculty presentation

  • Clinical decision-making for patients with disease progression on front-line chemobiologic therapy: Importance of RAS status, prior therapy, disease-free interval, performance status (PS) and other factors in the selection of second- and later-line therapy
  • Optimal sequencing of regorafenib and TAS-102 for patients with mCRC; use of clinical characteristics to inform this decision (eg, PS, hematologic reserve)
  • Clinical investigator perspectives on initial dosing and dose reduction or escalation strategies with regorafenib
  • Incidence and time course of common toxicities associated with regorafenib and TAS-102
  • Clinical trials evaluating TAS-102 and regorafenib as earlier-line therapy
  • Role, if any, of multiplex testing (ie, next-generation sequencing) after disease progression on multiple lines of therapy

MODULE 3: Existing, Recently Approved and Investigational Approaches for Patients with Pancreatic Adenocarcinoma (PAD) — Dr Chiorean

Topics to be reviewed during case discussion and faculty presentation

  • Available data with and current clinical indications for the use of nab paclitaxel/gemcitabine and FOLFIRINOX as (neo)adjuvant therapy
  • Importance of age, PS, comorbidities and patient preferences in the selection of first-line chemotherapy for metastatic PAD
  • Nanoliposomal formulation of nal-IRI and proposed effects on drug delivery and efficacy
  • Phase III efficacy and safety data with, patient selection for and practical integration of nal-IRI in relapsed disease
  • Promising agents and treatment strategies currently in development

MODULE 4: Novel Agents and Strategies in the Management of Hepatocellular Carcinoma (HCC) — Dr El-Khoueiry

Topics to be reviewed during case discussion and faculty presentation

  • Prevention, recognition and management of side effects associated with sorafenib in HCC
  • Sorafenib dosing in unique populations (Child-Pugh class B or C, elderly, poor PS)
  • Emerging results from the Phase III Study 304 comparing lenvatinib to sorafenib as first-line therapy for unresectable HCC
  • FDA approval of regorafenib as second-line therapy for patients with HCC progressing on sorafenib; optimal integration into current management algorithms
  • Early efficacy data with, current nonresearch role, if any, of and ongoing trials evaluating anti-PD-1/PD-L1 antibodies for patients with advanced HCC

MODULE 5: Protocol and Nonresearch Treatment Decision-Making for Patients with Locally Advanced or Metastatic Gastric/Gastroesophageal Junction (GEJ) Cancer — Dr Fuchs

Topics to be reviewed during case discussion and faculty presentation

  • Sequence and selection of systemic therapy for patients with newly diagnosed and progressive metastatic disease: Implications of HER2 status, prior (neo)adjuvant therapy, age/PS and disease-free interval
  • Evidence-based integration of ramucirumab into the clinical algorithms for metastatic gastric/GEJ cancer; ongoing Phase III clinical trials of ramucirumab (eg, RAINFALL)
  • Available safety and efficacy data with anti-PD-1/PD-L1 antibodies for advanced gastric/GEJ cancer (eg, ATTRACTION-2); current role, if any, in clinical practice
  • Ongoing trials evaluating immune checkpoint inhibitors in gastric/GEJ cancer
  • Biologic rationale for, early clinical trial data with and ongoing investigation of novel agents and strategies (eg, napabucasin, claudiximab, TAS-102, regorafenib)

MODULE 6: Potential Role of Immune Checkpoint Inhibitors in Patients with mCRC —
Dr Overman

Topics to be reviewed during case discussion and faculty presentation

  • Biologic function of DNA mismatch repair and consequences of its deficiency; MSI and hypermutability of cells
  • Incidence of MSI-high tumors in patients with CRC and other gastrointestinal cancers
  • Indications and guideline recommendations for MSI testing in patients with mCRC
  • Biologic rationale for responsiveness of MSI-high tumors to anti-PD-1/PD-L1 checkpoint inhibitors
  • Available data, current clinical role, if any, and ongoing trials with anti-PD-1/PD-L1 antibodies for MSI-high cancer
  • Clinical strategies under investigation to induce immune responses in patients with microsatellite stable CRC

Target Audience:
This program is intended for medical oncologists, hematology-oncology fellows and other allied healthcare professionals involved in the treatment of colorectal, gastroesophageal, pancreatic and hepatocellular cancer.

Learning Objectives and Goals:
At the conclusion of this activity, participants should be able to:

  • Appraise recent data on therapeutic advances and changing practice standards in colorectal, gastric, pancreatic and hepatocellular cancer, and integrate this information, as appropriate, into current clinical care.
  • Develop a long-term care plan for individuals diagnosed with metastatic colorectal cancer, considering the patient’s biomarker profile, tumor location, exposure to prior systemic therapy, symptomatology, performance status and personal goals of treatment.
  • Utilize HER2 status, clinical factors and patient perspectives to optimize the selection and sequence of systemic therapy for patients with locally advanced or metastatic gastric or gastroesophageal cancer.
  • Consider age, performance status, and other clinical and logistical factors in the selection of systemic therapy for patients with locally advanced or metastatic pancreatic cancer.
  • Communicate the benefits and risks of existing and emerging systemic interventions to patients with locally advanced or metastatic hepatocellular cancer.
  • Counsel patients regarding the incidence and manifestation of side effects and toxicities associated with commonly used systemic agents and regimens in the management of advanced colorectal, gastric, pancreatic and hepatocellular cancer.
  • Appraise the rationale for and clinical data with investigational anti-PD-1 and/or anti-PD-L1 antibodies for patients with gastrointestinal cancers.
  • Describe the proposed mechanisms of action of and recall new data with investigational agents demonstrating promising activity in colorectal, gastric, pancreatic and hepatocellular cancer, and use this information to refer appropriate patients for participation in ongoing trials.

CME Credit Form:
A CME credit form will be given to each participant at the conclusion of the activity.

Accreditation Statement:
Research To Practice is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.

Credit Designation Statement:
Research To Practice designates this live activity for a maximum of 2.5 AMA PRA Category 1 Credits ™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

Disclosure Policy:
Research To Practice (RTP) is committed to providing its participants with high-quality, unbiased and state-of-the-art education. We assess conflicts of interest with faculty, planners and managers of CME activities. Conflicts of interest are identified and resolved through a conflict of interest resolution process. In addition, all activity content is reviewed by both a member of the RTP scientific staff and an external, independent physician reviewer for fair balance, scientific objectivity of studies referenced and patient care recommendations. Financial disclosures will be provided in meeting course materials.

Supporters:
This activity is supported by educational grants from Astellas Pharma Global Development Inc, Bayer HealthCare Pharmaceuticals, Boston Biomedical Pharma Inc, Bristol-Myers Squibb Company, Celgene Corporation, Halozyme Inc, Ipsen Biopharmaceuticals Inc, Lilly and Taiho Oncology Inc.

Hilton Chicago
720 South Michigan Avenue
Chicago, IL 60605
Hotel Phone: (312) 922-4400

Meeting Room:
Grand Ballroom (Level 2)

Directions:
The Hilton Chicago hotel is located just 5 minutes (2.5 miles) north of the McCormick Place convention center, where the ASCO Annual Meeting is taking place.

 

Thank you for your interest in our educational program. At this time online preregistration is closed. However, seats are still available for the conference. Onsite registration will be open starting at 6:30 PM (Central Time) on Saturday, June 3rd. If you are interested in attending, please visit our registration desk in the Grand Ballroom foyer located on the second level of the Hilton Chicago hotel (720 Michigan Avenue, Chicago, IL).

Please note, onsite registrant seating will be prioritized for healthcare professionals directly involved in the care of patients. If you have any questions, please feel free to contact us via email at Meetings@ResearchToPractice.com or call (800) 233-6153.