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This document outlines the agenda for a weekly teleconference of the PRO-CTCAE Task 2 committee, discussing item development, decision-making, and item selection issues related to symptom assessment
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How to fill out PRO-CTCAE Task 2 (Item Development) Committee Weekly Telecon

01
Gather all committee members for the telecon.
02
Review the agenda and objectives for the meeting.
03
Assign roles such as note-taker and timekeeper.
04
Discuss the progress on item development since the last meeting.
05
Identify and address any challenges or roadblocks.
06
Brainstorm new items to be developed based on feedback.
07
Set deadlines for item completion and review.
08
Schedule the next telecon meeting.

Who needs PRO-CTCAE Task 2 (Item Development) Committee Weekly Telecon?

01
Members of the PRO-CTCAE Item Development Committee.
02
Researchers and clinicians involved in patient-reported outcome measures.
03
Stakeholders interested in developing and refining PRO-CTCAE items.
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People Also Ask about

The preferred recall period for the PRO-CTCAE is the past 7 days, although investigators may opt for recall periods of 2, 3, or 4 weeks with an understanding that there may be some information loss.
CTCAE stands for Common Terminology Criteria for Adverse Events; these criteria are also called "common toxicity criteria." In CTCAE, an adverse event (AE) is defined as any abnormal clinical finding temporally associated with the use of a therapy for cancer; causality is not required.
CTCAE version 6.0 is expected in the fall of 2024.
PRO-CTCAE responses are scored from 0 to 4 (or 0/1 for absent/present). Ped-PRO-CTCAE module responses are scored from 0 to 3 (or 0/1 for absent/present). PRO-CTCAE and the Ped-PRO-CTCAE module yield up to three patient-reported scores per symptomatic toxicity.
Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE®) Home. Data & Tools.
The PRO version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) has been recommended as a useful instrument to assess the latter (2,3). The PRO-CTCAE is a library of 124 items characterizing 78 symptomatic toxicities in terms of frequency, severity, interference, and/or presence or absence (4).
PRO-CTCAE responses are scored from 0 to 4 (or 0/1 for absent/present). Ped-PRO-CTCAE module responses are scored from 0 to 3 (or 0/1 for absent/present). PRO-CTCAE and the Ped-PRO-CTCAE module yield up to three patient-reported scores per symptomatic toxicity.
CTCAE version 6.0 is expected in the fall of 2024.

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The PRO-CTCAE Task 2 (Item Development) Committee Weekly Telecon is a regular meeting where committee members discuss the development of patient-reported outcomes in clinical trials, focusing on creating and refining measurement items.
Members of the PRO-CTCAE Task 2 (Item Development) Committee are required to participate and file the necessary reports pertaining to the telecon.
Participants typically fill out a structured form that includes details of discussions, decisions made, action items, and any relevant data sharing during the teleconference.
The purpose is to facilitate collaboration among committee members, ensure progress on item development, and address any challenges or issues that arise during the development process.
Information reported typically includes attendance, key discussion points, decisions made, outstanding action items, and timelines for future tasks related to item development.
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