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Multicenter Study
. 2022 Jan 14;17(1):e0261565.
doi: 10.1371/journal.pone.0261565. eCollection 2022.

PET metabolic tumor volume as a new prognostic factor in childhood rhabdomyosarcoma

Affiliations
Multicenter Study

PET metabolic tumor volume as a new prognostic factor in childhood rhabdomyosarcoma

Helio Fayolle et al. PLoS One. .

Abstract

Purpose: Childhood RMS is a rare malignant disease in which evaluation of tumour spread at diagnosis is essential for therapeutic management. F-18 FDG-PET imaging is currently used for initial RMS disease staging.

Materials and methods: This multicentre retrospective study in six French university hospitals was designed to analyse the prognostic accuracy of MTV at diagnosis for patients with RMS between 1 January 2007 and 31 October 2017, for overall (OS) and progression-free survival (PFS). MTV was defined as the sum of the primitive tumour and the largest metastasis, where relevant, with a 40% threshold of the primary tumour SUVmax. Additional aims were to define the prognostic value of SUVmax, SUVpeak, and bone lysis at diagnosis.

Results: Participants were 101 patients with a median age of 7.4 years (IQR [4.0-12.5], 62 boys), with localized disease (35 cases), regional nodal spread (43 cases), or distant metastases (23). 44 patients had alveolar subtypes. In a univariate analysis, a MTV greater than 200 cm3 was associated with OS (HR = 3.47 [1.79;6.74], p<0.001) and PFS (HR = 3.03 [1.51;6.07], p = 0.002). SUVmax, SUVpeak, and bone lysis also influenced OS (respectively p = 0.005, p = 0.004 and p = 0.007) and PFS (p = 0.029, p = 0.019 and p = 0.015). In a multivariate analysis, a MTV greater than 200 cm3 was associated with OS (HR = 2.642 [1.272;5.486], p = 0.009) and PFS (HR = 2.707 [1.322;5.547], p = 0.006) after adjustment for confounding factors, including SUVmax, SUVpeak, and bone lysis.

Conclusion: A metabolic tumor volume greater than 200 cm3, SUVmax, SUVpeak, and bone lysis in the pre-treatment assessment were unfavourable for outcome.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Flowchart.
N: number of patients.
Fig 2
Fig 2. Lumbar-aortic lymph node involvement in a 7-year-old child with a pelvic alveolar RMS.
Metabolic tumour volume represents all the voxels within the initial volume of interest with SUV values equal to or above an automatic threshold of 40% of SUVmax. A) CT scan: the volume is hardly measurable, mainly owing to the presence of extensive necrosis. B) Fused PET-CT with metabolic tumour volume, SUVmax and SUVpeak.
Fig 3
Fig 3. Left mandibular isolated primary tumour in a 4-year-old child with embryonal RMS.
Primary tumour lysis of the left mounting mandibular branch. A) CT scan only in bone window. B) Fused PET-CT in bone window. C) CT scan only in soft-tissue window. D) Fused PET-CT in soft-tissue window.
Fig 4
Fig 4
A) Overall survival. B) Progression-free survival.
Fig 5
Fig 5. Overall survival according to MTV.
Fig 6
Fig 6. Progression-free survival according to MTV.

References

    1. Howlader N, Noone AM, Krapcho M, Miller D, Brest A, Yu M, et al.. (eds). SEER Cancer Statistics Review, 1975–2017, National Cancer Institute. Bethesda, MD, https://seer.cancer.gov/csr/1975_2017/, based on November 2019 SEER data submission, posted to the SEER web site, April 2020.
    1. Hawkins DS, Spunt SL, Skapek SX, COG Soft Tissue Sarcoma Committee. Children’s Oncology Group’s 2013 blueprint for research: Soft tissue sarcomas. Pediatr Blood Cancer. June 2013;60(6):1001–8. doi: 10.1002/pbc.24435 - DOI - PMC - PubMed
    1. Panda SP, Chinnaswamy G, Vora T, Prasad M, Bansal D, Kapoor G, et al.. Diagnosis and Management of Rhabdomyosarcoma in Children and Adolescents: ICMR Consensus Document. Indian J Pediatr. May 2017;84(5):393–402. doi: 10.1007/s12098-017-2315-3 - DOI - PubMed
    1. Van Rijn RR, Wilde JCH, Bras J, Oldenburger F, McHugh KMC, Merks JHM. Imaging findings in noncraniofacial childhood rhabdomyosarcoma. Pediatr Radiol. June 2008;38(6):617–34. doi: 10.1007/s00247-008-0751-y - DOI - PMC - PubMed
    1. Chung EM, Smirniotopoulos JG, Specht CS, Schroeder JW, Cube R. Pediatric Orbit Tumors and Tumorlike Lesions: Nonosseous Lesions of the Extraocular Orbit. RadioGraphics. Nov 2007;27(6):1777–99. doi: 10.1148/rg.276075138 - DOI - PubMed

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