Cancer Medicine (Feb 2021)

Metabolic response as assessed by 18F‐fluorodeoxyglucose positron emission tomography‐computed tomography does not predict outcome in patients with intermediate‐ or high‐risk rhabdomyosarcoma: A report from the Children's Oncology Group Soft Tissue Sarcoma Committee

  • Douglas J. Harrison,
  • Yueh‐Yun Chi,
  • Jing Tian,
  • Pooja Hingorani,
  • Leo Mascarenhas,
  • Geoffrey B. McCowage,
  • Brenda J. Weigel,
  • Rajkumar Venkatramani,
  • Suzanne L. Wolden,
  • Torunn I. Yock,
  • David A. Rodeberg,
  • Andrea A. Hayes‐Jordan,
  • Lisa A. Teot,
  • Sheri L. Spunt,
  • William H. Meyer,
  • Douglas S. Hawkins,
  • Barry L. Shulkin,
  • Marguerite T. Parisi

DOI
https://doi.org/10.1002/cam4.3667
Journal volume & issue
Vol. 10, no. 3
pp. 857 – 866

Abstract

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ABSTRACT Background Strategies to optimize management in rhabdomyosarcoma (RMS) include risk stratification to assign therapy aiming to minimize treatment morbidity yet improve outcomes. This analysis evaluated the relationship between complete metabolic response (CMR) as assessed by 18F‐fluorodeoxyglucose positron emission tomography‐computed tomography (FDG‐PET) imaging and event‐free survival (EFS) in intermediate‐risk (IR) and high‐risk (HR) RMS patients. Methods FDG‐PET imaging characteristics, including assessment of CMR and maximum standard uptake values (SUVmax) of the primary tumor, were evaluated by central review. Institutional reports of SUVmax were used when SUVmax values could not be determined by central review. One hundred and thirty IR and 105 HR patients had FDG‐PET scans submitted for central review or had SUVmax data available from institutional report at any time point. A Cox proportional hazards regression model was used to evaluate the relationship between these parameters and EFS. Results SUVmax at study entry did not correlate with EFS for IR (p = 0.32) or HR (p = 0.86) patients. Compared to patients who did not achieve a CMR, EFS was not superior for IR patients who achieved a CMR at weeks 4 (p = 0.66) or 15 (p = 0.46), nor for HR patients who achieved CMR at week 6 (p = 0.75) or 19 (p = 0.28). Change in SUVmax at week 4 (p = 0.21) or 15 (p = 0.91) for IR patients or at week 6 (p = 0.75) or 19 (p = 0.61) for HR patients did not correlate with EFS. Conclusion Based on these data, FDG‐PET does not appear to predict EFS in IR or HR‐RMS. It remains to be determined whether FDG‐PET has a role in predicting survival outcomes in other RMS subpopulations.

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