SITC is committed to maintaining full transparency in our clinical practice guideline development process, in alignment with the Institute of Medicine’s standards, for the ultimate purpose of developing quality clinical practice guidelines to aid practitioners in providing the best possible care to their patients. The public open comment period allows for key stakeholders and other experts in the field – both within and outside of our membership – to provide comment on the confidential manuscript draft prior to publication.  

SITC clinical practice guidelines equip clinicians with the knowledge to utilize newly approved agents, guidance on patient selection, biomarker testing, and management of immune-related toxicities, in addition to providing expert insight for what’s on the horizon in immunotherapy treatment options. 

Instructions for Requesting Draft Manuscript

All participants must complete and sign a non-disclosure and confidentiality agreement prior to obtaining the draft manuscript. All comments must be received by the noted deadline to be considered. 

• Download the non-disclosure and confidentiality agreement 
  
• Email the completed document to scientificresources@sitcancer.org
  
• A copy of the draft guideline will be sent within 1-2 business days after receipt of the complete agreement
  
• Further instructions about how to provide comment will be included with the draft (anonymous comments will not be accepted)
  

Manuscripts Available for Comment