Proton versus photon radiation therapy for patients with high‐risk neuroblastoma: The need for a customized approach. Issue 10 (4th June 2013)
- Record Type:
- Journal Article
- Title:
- Proton versus photon radiation therapy for patients with high‐risk neuroblastoma: The need for a customized approach. Issue 10 (4th June 2013)
- Main Title:
- Proton versus photon radiation therapy for patients with high‐risk neuroblastoma: The need for a customized approach
- Authors:
- Hill‐Kayser, Christine
Tochner, Zelig
Both, Stefan
Lustig, Robert
Reilly, Anne
Balamuth, Naomi
Womer, Richard
Maris, John
Grupp, Stephen
Bagatell, Rochelle - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="pbc24606-sec-0001" sec-type="section"> <title>Background</title> <p>Proton therapy for treatment for high‐risk neuroblastoma may offer sparing of organs at risk (OAR) when compared to intensity‐modulated X‐ray therapy (IMXT).</p> </sec> <sec id="pbc24606-sec-0002" sec-type="section"> <title>Procedure</title> <p>Double‐scattered proton plans and IMXT plans delivering 2, 160 cGy to the primary tumor site and other residual disease were developed for 13 consecutive HR‐NBL patients. Radiation doses to target volumes and OAR were calculated to determine the optimal modality for each.</p> </sec> <sec id="pbc24606-sec-0003" sec-type="section"> <title>Results</title> <p>All patients received radiation (5/13 ≥ 2 sites). No patient has experienced local recurrence or clinical organ toxicity. Coverage was excellent using both protons and IMXT: median % dose delivered to 95% clinical target volume was 99% and 100%, respectively. For nine patients with lateralized disease, proton therapy offered sparing of the contralateral kidney both with regard to median dose and dose to 20% (median &lt;1 cGy vs. 362 cGy, <italic>P</italic> = 0.01; median 100 cGy vs. 634 cGy, <italic>P</italic> = 0.02, respectively). Proton therapy did not reduce ipsilateral kidney dose, and for 2 select patients with lateralized disease IMXT improved overall bilateral renal sparing. Proton therapy improved median bowel (median 33 cGy vs.<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="pbc24606-sec-0001" sec-type="section"> <title>Background</title> <p>Proton therapy for treatment for high‐risk neuroblastoma may offer sparing of organs at risk (OAR) when compared to intensity‐modulated X‐ray therapy (IMXT).</p> </sec> <sec id="pbc24606-sec-0002" sec-type="section"> <title>Procedure</title> <p>Double‐scattered proton plans and IMXT plans delivering 2, 160 cGy to the primary tumor site and other residual disease were developed for 13 consecutive HR‐NBL patients. Radiation doses to target volumes and OAR were calculated to determine the optimal modality for each.</p> </sec> <sec id="pbc24606-sec-0003" sec-type="section"> <title>Results</title> <p>All patients received radiation (5/13 ≥ 2 sites). No patient has experienced local recurrence or clinical organ toxicity. Coverage was excellent using both protons and IMXT: median % dose delivered to 95% clinical target volume was 99% and 100%, respectively. For nine patients with lateralized disease, proton therapy offered sparing of the contralateral kidney both with regard to median dose and dose to 20% (median &lt;1 cGy vs. 362 cGy, <italic>P</italic> = 0.01; median 100 cGy vs. 634 cGy, <italic>P</italic> = 0.02, respectively). Proton therapy did not reduce ipsilateral kidney dose, and for 2 select patients with lateralized disease IMXT improved overall bilateral renal sparing. Proton therapy improved median bowel (median 33 cGy vs. 590 cGy, <italic>P</italic> = 0.01), total body (median &lt;1 cGy vs. 30 cGy, <italic>P</italic> = 0.15), and liver dose (median &lt;1 cGy vs. 529, <italic>P</italic> &lt; 0.001). When chest RT was required, proton therapy decreased median heart dose and mean lung dose.</p> </sec> <sec id="pbc24606-sec-0004" sec-type="section"> <title>Conclusions</title> <p>For most patients (11/13), proton therapy offered the optimal combination of target coverage and organ sparing, and is a feasible treatment for HR‐NBL. We recommend a customized approach with careful evaluation of renal dosimetry; IMXT may be preferred for select patients. Pediatr Blood Cancer 2013;60:1606–1611. © 2013 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatric blood & cancer. Volume 60:Issue 10(2013:Oct.)
- Journal:
- Pediatric blood & cancer
- Issue:
- Volume 60:Issue 10(2013:Oct.)
- Issue Display:
- Volume 60, Issue 10 (2013)
- Year:
- 2013
- Volume:
- 60
- Issue:
- 10
- Issue Sort Value:
- 2013-0060-0010-0000
- Page Start:
- 1606
- Page End:
- 1611
- Publication Date:
- 2013-06-04
- Subjects:
- Tumors in children -- Periodicals
Blood -- Diseases -- Periodicals
Cancer in children -- Periodicals
618.92 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1545-5017 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pbc.24606 ↗
- Languages:
- English
- ISSNs:
- 1545-5009
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.533500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3475.xml