PASSReviewer 1· 90% conf
Reporting is generally transparent: methods are detailed, trial is registered, all outcomes are reported, limitations are discussed, and conclusions are proportional. However, no explicit reference to a reporting guideline is made.
Evidence
direct quote[Methods, Trial Design and Treatment]
“NCT02912559 (https://clinicaltrials.gov/ct2/show/NCT02912559)”direct quote[Discussion, paragraph 3]
“ATOMIC was not designed to test the benefit of atezolizumab in the absence of standard chemotherapy.”absence[Methods]
No reporting guideline is referenced.PASSReviewer 2· 85% conf
The paper is generally transparent, with a trial registration, detailed methods, limitations discussion, and proportional conclusions. However, it does not explicitly reference a reporting guideline (e.g., CONSORT) and some secondary outcomes are deferred to future reports.
Evidence
direct quote[Methods, Trial Design and Treatment]
“NCT02912559 (https://clinicaltrials.gov/ct2/show/NCT02912559)”absence[Methods, Discussion]
No reference to CONSORT or other reporting guideline.direct quote[Methods, Statistical Analysis]
“The secondary endpoints of patient-reported outcome-CTCAE (PRO-CTCAE) and quality of life will be reported separately.”