TABLE 1

Summary of Studies of 18F-FDG PET for Early Prediction of Treatment Response

18F-FDG PET metabolic response
ReferenceYearNo. of patients included in 18F-FDG PET analysisPathologic response criteria*Percentage of respondersAfter indicated treatment cycleDecrease in SUVPercentage sensitivityPercentage specificityPercentage negative predictive value
Schelling et al. (8)200022pCR + pMRD29First, second>45% after first or second100 (first), 83 (second)85 (first), 94 (second)N/A
Smith et al. (9)200030pCR-macro38First>20%9074N/A
Rousseau et al. (10)200664>50% therapeutic effect56First, second>40% after first or second61 (first), 89 (second)96 (first), 95 (second)68 (first), 85 (second)
Schwarz-Dose (11)2009104pCR + pMRD16First, second>45% after first, >55% after second736390
Humbert et al. (32)201237pCR38First>75%648379
Groheux et al. (35)201330pCR53Second>62%8663N/A
SUV ≤ 3.0§869488
Humbert et al. (34)201454pCR41First>60%835284
SUV < 2.1§598876
  • * pCR = pathologic complete response, defined as absence of residual invasive tumor in breast, irrespective of lymph node status [ypT0/is ypNX], unless otherwise indicated; pMRD = minimal residual disease, defined as a few scattered foci of microscopic residual invasive tumor (≤2 mm); pCR-macro = pathologic response, defined as absence of macroscopically visible tumor.

  • pCR was defined as absence of residual invasive tumor in both breast and axillary lymph nodes [ypT0/is ypN0].

  • Results were based on HER2-positive breast cancers only.

  • § Absolute SUVs for defining cutoff values.

  • N/A = not available.