<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Jingu K</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>To evaluate the safety of focal dose escalation to regions with standardized uptake value (SUV) >2.0 using intensity-modulated radiation therapy (IMRT) by comparison of radiotherapy plans using dose-volume histograms (DVHs) and normal tissue complication probability (NTCP) for postoperative local recurrent rectal cancer&lt;h4>Methods&lt;/h4>First, we performed conventional radiotherapy with 40 Gy/20 fr. (CRT 40 Gy) for 12 patients with postoperative local recurrent rectal cancer, and then we performed FDG-PET/CT radiotherapy planning for those patients. We defined the regions with SUV > 2.0 as biological target volume (BTV) and made three boost plans for each patient: 1) CRT boost plan, 2) IMRT without dose-painting boost plan, and 3) IMRT with dose-painting boost plan. The total boost dose was 20 Gy. In IMRT with dose-painting boost plan, we increased the dose for BTV+5 mm by 30% of the prescribed dose. We added CRT boost plan to CRT 40 Gy (summed plan 1), IMRT without dose-painting boost plan to CRT 40 Gy (summed plan 2) and IMRT with dose-painting boost plan to CRT 40 Gy (summed plan 3), and we compared those plans using DVHs and NTCP.&lt;h4>Results&lt;/h4>D(mean) of PTV-PET and that of PTV-CT were 26.5 Gy and 21.3 Gy, respectively. V50 of small bowel PRV in summed plan 1 was significantly higher than those in other plans ((summed plan 1 vs. summed plan 2 vs. summed plan 3: 47.11 +/- 45.33 cm3 vs. 40.63 +/- 39.13 cm3 vs. 41.25 +/- 39.96 cm3 (p &lt; 0.01, respectively)). There were no significant differences in V30, V40, V60, D(mean) or NTCP of small bowel PRV.&lt;h4>Conclusions&lt;/h4>FDG-PET-guided IMRT can facilitate focal dose-escalation to regions with SUV above 2.0 for postoperative local recurrent rectal cancer.</pubmed_abstract><journal>BMC cancer</journal><pagination>127</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2858110</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Focal dose escalation using FDG-PET-guided intensity-modulated radiation therapy boost for postoperative local recurrent rectal cancer: a planning study with comparison of DVH and NTCP.</pubmed_title><pmcid>PMC2858110</pmcid><pubmed_authors>Kaneta T</pubmed_authors><pubmed_authors>Koto M</pubmed_authors><pubmed_authors>Mitsuya M</pubmed_authors><pubmed_authors>Yamada S</pubmed_authors><pubmed_authors>Katja L</pubmed_authors><pubmed_authors>Matsufuji N</pubmed_authors><pubmed_authors>Ariga H</pubmed_authors><pubmed_authors>Fujimoto K</pubmed_authors><pubmed_authors>Jingu K</pubmed_authors><pubmed_authors>Ogawa Y</pubmed_authors><pubmed_authors>Metoki T</pubmed_authors><pubmed_authors>Takahashi S</pubmed_authors><pubmed_authors>Narazaki K</pubmed_authors><pubmed_authors>Takeda K</pubmed_authors><pubmed_authors>Umezawa R</pubmed_authors><pubmed_authors>Nemoto K</pubmed_authors><pubmed_authors>Takai Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Focal dose escalation using FDG-PET-guided intensity-modulated radiation therapy boost for postoperative local recurrent rectal cancer: a planning study with comparison of DVH and NTCP.</name><description>&lt;h4>Background&lt;/h4>To evaluate the safety of focal dose escalation to regions with standardized uptake value (SUV) >2.0 using intensity-modulated radiation therapy (IMRT) by comparison of radiotherapy plans using dose-volume histograms (DVHs) and normal tissue complication probability (NTCP) for postoperative local recurrent rectal cancer&lt;h4>Methods&lt;/h4>First, we performed conventional radiotherapy with 40 Gy/20 fr. (CRT 40 Gy) for 12 patients with postoperative local recurrent rectal cancer, and then we performed FDG-PET/CT radiotherapy planning for those patients. We defined the regions with SUV > 2.0 as biological target volume (BTV) and made three boost plans for each patient: 1) CRT boost plan, 2) IMRT without dose-painting boost plan, and 3) IMRT with dose-painting boost plan. The total boost dose was 20 Gy. In IMRT with dose-painting boost plan, we increased the dose for BTV+5 mm by 30% of the prescribed dose. We added CRT boost plan to CRT 40 Gy (summed plan 1), IMRT without dose-painting boost plan to CRT 40 Gy (summed plan 2) and IMRT with dose-painting boost plan to CRT 40 Gy (summed plan 3), and we compared those plans using DVHs and NTCP.&lt;h4>Results&lt;/h4>D(mean) of PTV-PET and that of PTV-CT were 26.5 Gy and 21.3 Gy, respectively. V50 of small bowel PRV in summed plan 1 was significantly higher than those in other plans ((summed plan 1 vs. summed plan 2 vs. summed plan 3: 47.11 +/- 45.33 cm3 vs. 40.63 +/- 39.13 cm3 vs. 41.25 +/- 39.96 cm3 (p &lt; 0.01, respectively)). There were no significant differences in V30, V40, V60, D(mean) or NTCP of small bowel PRV.&lt;h4>Conclusions&lt;/h4>FDG-PET-guided IMRT can facilitate focal dose-escalation to regions with SUV above 2.0 for postoperative local recurrent rectal cancer.</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Apr</publication><modification>2024-11-12T16:27:32.271Z</modification><creation>2019-03-27T00:30:17Z</creation></dates><accession>S-EPMC2858110</accession><cross_references><pubmed>20374623</pubmed><doi>10.1186/1471-2407-10-127</doi></cross_references></HashMap>