Adaptive Proton Therapy for Pediatric Parameningeal Rhabdomyosarcoma: On-Treatment Anatomic Changes and Timing to Replanning

To characterize on-treatment changes in GTV morphology in children with parameningeal rhabdomyosarcoma receiving upfront proton therapy with concurrent chemotherapy and thereby provide guidance on the timing of on-treatment imaging and adaptive replanning. GTV was delineated on 86 simulation and wee...

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Veröffentlicht in:Clinical oncology (Royal College of Radiologists (Great Britain)) 2023-04, Vol.35 (4), p.245-254
Hauptverfasser: Uh, J., Jordan, J.A., Pappo, A.S., Krasin, M.J., Hua, C.
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Sprache:eng
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Zusammenfassung:To characterize on-treatment changes in GTV morphology in children with parameningeal rhabdomyosarcoma receiving upfront proton therapy with concurrent chemotherapy and thereby provide guidance on the timing of on-treatment imaging and adaptive replanning. GTV was delineated on 86 simulation and weekly MR images of 15 prospectively enrolled patients (aged 1–21 years). Temporal changes from baseline in volume and surface (95% Hausdorff distance) were analyzed in relation to the need for plan verification and the resultant doses with hypothetical no treatment adaptation. The median time was 6 days from the initiation of chemotherapy to CT+MR simulation and 15 days from the simulation to the start of radiotherapy. All but 1 patient showed a continuous decrease in GTV (0.16–1.52%/day) after simulation. At 3 weeks from simulation, 10 of 15 patients exhibited a significant reduction in volume (median, 20%; range, 6–29%). Without replanning, these changes could lead to a reduction in CTV V95 by 7–14% (n = 2) and/or an increase in D0.01 cc/Dmean of adjacent organs at risk by 6–21% of the prescribed target dose (n = 7). Significant dosimetric consequences occurred in cases with (1) a considerable weight gain, (2) shrinkage of the skin surface, or (3) tumor regression in the oral or nasal cavity and sinus that altered air-tissue components in the beam path. The subsequent GTV and dosimetry after 3 weeks from simulation (4 weeks from chemotherapy initiation) demonstrated a relatively stable trend. On-treatment imaging at 3 weeks after simulation is recommended, if the simulation is performed at 1 week after the initiation of chemotherapy, to detect significant anatomic changes that could result in >5% deviation from planned target coverage and/or organ doses in pediatric patients with parameningeal rhabdomyosarcoma receiving early proton therapy. •An early GTV change is common in paediatric PM RMS receiving upfront proton therapy.•Target underdose and/or OAR overdosage may occur without adaptation to new anatomy.•Care should be taken when proton beams intersect variable air–tissue interfaces.•On-treatment imaging at 3 weeks from RT simulation was beneficial in our cohort.
ISSN:0936-6555
1433-2981
DOI:10.1016/j.clon.2023.01.013