National Cancer InstituteU.S. National Institutes of Healthwww.cancer.gov

CTWG Steering Committee System

The Steering Committees strive to enhance the National Cancer Clinical Trials Enterprise through the implementation of Prioritization/Scientific Quality Initiatives 1, 2, and 3 of the CTWG Report (PDF - 366KB).

Goals of the Committees

Scientific Steering Committees (SSCs) are composed of leading cancer experts and advocates from outside the Institute as well as NCI senior investigators who meet regularly to:

  • increase the transparency and openness of the trial design and prioritization process;
  • enhance patient advocate and community oncologist involvement in clinical trial design and prioritization;
  • convene Clinical Trial Planning Meetings to identify critical questions, unmet needs, and prioritize key strategies.

SSCs may establish one or more Task Forces and/or Working Groups that focus on specific diseases or scientific areas of interest.

Disease-Specific Steering Committees (DSSC):

Breast Cancer Steering Committee

Gastrointestinal Steering Committee

Genitourinary Steering Committee

Gynecologic Steering Committee

Head and Neck Steering Committee

Thoracic Malignancy Steering Committee

Roles of the Committees
are to:

Leverage current Intergroup, Cooperative Group, SPORE, and Cancer Center structures by:

  • increasing information exchange at an early stage of trial development;
  • increasing the efficiency of clinical trial collaboration;
  • reducing trial redundancy (phase II and phase III);
  • developing, evaluating, and prioritizing concepts for phase III and large phase II clinical trials.

Investigational Drug Steering Committee (IDSC)

Role of the Committee is to:

  • achieve optimal phase I and phase II trial designs for the most promising agents;
  • increase the predictive value of early phase trials, in order to design more successful phase III trials.

Symptom Management and Health-Related Quality of Life Steering Committee (SxQOL)

Role of the Committee is to:

  • review and prioritize symptom management intervention clinical trial concepts to be conducted through the CCOP mechanism;
  • provide input to studies with secondary quality-of-life (QOL) endpoints in cooperative group treatment studies;
  • develop prioritization criteria for QOL studies that are eligible for proposed correlative science/QOL set aside funds.

Patient Advocate Steering Committee

Role of the Committee is to:

  • develop and share best practices for patient advocates in Scientific Steering Committees;
  • identify common concerns and needs and propose potential solutions to address theses concerns;
  • disseminate Scientific Steering Committee information to the appropriate communities;
  • ensure that the concept evaluations consider the patient community at large, with a special focus on minority and underserved populations.

Clinical Trials Planning Meetings (CTPMs)

The goal of CTPMs is to:

  • bring together investigators from a variety of disciplines to develop strategic agendas for clinical trials in a specific field for the next 3-5 years;
  • facilitate innovation and collaboration among the broad oncology community active in the specific cancer under study;
  • to reach consensus on the most important clinical trials to conduct;
  • to develop the next phase III trials, or if that is not yet possible, to frame the phase II studies that will generate phase III questions.