483PD - The declaration of new lesions as a major factor of local-central discrepancy during a RECIST phase II trial

Date 21 December 2015
Event ESMO Asia 2015 Congress
Session Basic Science, biomarkers, new diagnostics and translational research
Topics Clinical research
Translational Research
Basic Scientific Principles
Basic Principles in the Management and Treatment (of cancer)
Presenter Hubert Beaumont
Citation Annals of Oncology (2015) 26 (suppl_9): 148-152. 10.1093/annonc/mdv533
Authors H. Beaumont1, T.L. Evans2, S.R. Hong3, M. Chadjaa4, Z. Monostori5
  • 1Science, MEDIAN Technologies, 06560 - Valbonne/FR
  • 2Clinical Medicine, University of Pennsylvania-Perelman Center for Advanced Medicine, Philadelphia/US
  • 3Department Of Radiology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul/KR
  • 4Clinial Research, SANOFI, vitry-sur-seine/FR
  • 5Department Of Radiology, National Koranyi Institute of Pulmonology, Budapest/HU



Dual readings of images by local investigators (LI) and central review (CR) can result in discordant interpretations. Variability of measurements and lack of conformance to response criteria were previously analyzed. Our study compares LI/CR sensitivity at detecting new lesions (NL) and the consequences on the discordances.


A RECIST 1.1 Randomized Phase II clinical trial of Cabazitaxel versus Topotecan enrolled 179 relapsing adult patients if meeting histological/cytological proven locally advanced or metastatic small cell lung cancer. Sixty-six LI and one CR were involved. When LI and CR disagreed on progressive disease, an additional reader (ADD) reviewed all patient images while blinded from other readers' assessments. New Lesions declared by LI, CR or ADD were retrospectively checked for presence/absence of lesions at current and previous time points.


36.7% of patient follow-ups required ADD assessment. The majority of disagreements (53%) came from NL declaration. CR detected 18.9% more NLs than did LI. CR reported four times more lung NLs, while LI reported 36% more nodal NLs. LI/CR reported similar numbers of NLs in the brain (38 vs. 33) and liver (36 vs. 39). 96.8% (30/31) of ADD reviewed patients with reported NL by LI/CR, displayed effectively what can be interpreted as NLs. LI, CR and ADD detected respectively 54.8 % [36.0; 72.7], 67.7% [48; 83.3] and 35.5% [19.2; 54.6] of these patients. 53% of nodal NL were debatable as having a shortest axial diameter (SAD) smaller than 15mm or larger than 10mm at the previous time point or a difference of SAD between time points smaller than 5mm. We also analyzed patients for which both LI and CR detected NLs. For 44.5% (4/9) of these patients, LI and CR detected NL at same time point. For 44.5% (4/9) patients, NLs were detected first by CR and, for 11.0% (1/9) patients, LI detected NL first.


The sensitivity of readers in the detection of NLs was the main cause of disagreement. LI had a lower sensitivity on new lung lesions than did CR. Optimizing the criteria defining nodal NL would help reduce disagreements. CR anticipated the response due to a better sensitivity in detecting NLs. Blinding ADD from other readers' findings is questionable.

Clinical trial identification

Present retrospective study is based on NCT01500720 clinical trial (www.clinicaltrial.gouv) data (Image and annotations)


All authors have declared no conflicts of interest.