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dc.contributor.authorMillion, Lynn
dc.contributor.authorLaurie, Frances
dc.contributor.authorMorano, Karen
dc.contributor.authorFitzGerald, Thomas J.
dc.date2022-08-11T08:08:26.000
dc.date.accessioned2022-08-23T15:55:26Z
dc.date.available2022-08-23T15:55:26Z
dc.date.issued2021-02-03
dc.date.submitted2021-04-29
dc.identifier.citation<p>Million L, Hayes-Jordan A, Chi YY, Donaldson SS, Wolden S, Morris C, Terezakis S, Laurie F, Morano K, Fitzgerald TJ, Yock TI, Rodeberg DA, Anderson JR, Speights RA, Black JO, Coffin C, McCarville MB, Kao SC, Hawkins DS, Spunt SL, Randall RL. Local Control For High-Grade Nonrhabdomyosarcoma Soft Tissue Sarcoma Assigned to Radiation Therapy on ARST0332: A Report From the Childrens Oncology Group. Int J Radiat Oncol Biol Phys. 2021 Feb 3:S0360-3016(21)00125-5. doi: 10.1016/j.ijrobp.2021.01.051. Epub ahead of print. PMID: 33548339. <a href="https://doi.org/10.1016/j.ijrobp.2021.01.051">Link to article on publisher's site</a></p>
dc.identifier.issn0360-3016 (Linking)
dc.identifier.doi10.1016/j.ijrobp.2021.01.051
dc.identifier.pmid33548339
dc.identifier.urihttp://hdl.handle.net/20.500.14038/29753
dc.description<p>Full author list omitted for brevity. For the full list of authors, see article.</p>
dc.description.abstractPURPOSE: The ARST0332 trial for pediatric and young adults with nonrhabdomyosarcoma soft tissue sarcoma (NRSTS) used risk-based treatment including primary resection with lower-than-standard radiation doses to optimize local control (LC) while minimizing long-term toxicity in those requiring radiation therapy (RT). RT for high-grade NRSTS was based on extent of resection (R0: negative margins, R1: microscopic margins, R2/U: gross disease/unresectable); those with > 5 cm tumors received chemotherapy (CT; ifosfamide/doxorubicin). This analysis evaluates LC for patients assigned to RT and prognostic factors associated with local recurrence (LR). METHODS AND MATERIALS: Patients aged < 30 years with high-grade NRSTS received RT (55.8 Gy) for R1 < /=5 cm tumor (arm B); RT (55.8 Gy)/CT for R0/R1 > 5 cm tumor (arm C); or neoadjuvant RT (45 Gy)/CT plus delayed surgery, CT, and postoperative boost to 10.8 Gy R0 < 5 mm margins/R1 or 19.8 Gy for R2/unresected tumors (arm D). RESULTS: One hundred ninety-three eligible patients had 24 LRs (arm B 1/15 [6.7%], arm C 7/65 [10.8%], arm D 16/113 [14.2%]) at median time to LR of 1.1 years (range, 0.11-5.27). Of 95 eligible for delayed surgery after neoadjuvant therapy, 89 (93.7%) achieved R0/R1 margins. Overall LC after RT were as follows: R0, 106 of 109 (97%); R1, 51 of 60 (85%); and R2/unresectable, 2 of 6 (33%). LR predictors include extent of delayed resection (P < .001), imaging response before delayed surgery (P < .001), histologic subtype (P < .001), and no RT (P = .046). The 5-year event-free survival was significantly lower (P = .0003) for patients unable to undergo R0/R1 resection. CONCLUSIONS: Risk-based treatment for young patients with high-grade NRSTS treated on ARST0332 produced very high LC, particularly after R0 resection (97%), despite lower-than-standard RT doses. Neoadjuvant CT/RT enabled delayed R0/R1 resection in most patients and is preferred over adjuvant therapy due to the lower RT dose delivered.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=33548339&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1016/j.ijrobp.2021.01.051
dc.subjectBiological and Chemical Physics
dc.subjectNeoplasms
dc.subjectOncology
dc.subjectPediatrics
dc.subjectRadiation Medicine
dc.titleLocal Control For High-Grade Nonrhabdomyosarcoma Soft Tissue Sarcoma Assigned to Radiation Therapy on ARST0332: A Report From the Childrens Oncology Group
dc.typeJournal Article
dc.source.journaltitleInternational journal of radiation oncology, biology, physics
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/1965
dc.identifier.contextkey22709438
html.description.abstract<p>PURPOSE: The ARST0332 trial for pediatric and young adults with nonrhabdomyosarcoma soft tissue sarcoma (NRSTS) used risk-based treatment including primary resection with lower-than-standard radiation doses to optimize local control (LC) while minimizing long-term toxicity in those requiring radiation therapy (RT). RT for high-grade NRSTS was based on extent of resection (R0: negative margins, R1: microscopic margins, R2/U: gross disease/unresectable); those with > 5 cm tumors received chemotherapy (CT; ifosfamide/doxorubicin). This analysis evaluates LC for patients assigned to RT and prognostic factors associated with local recurrence (LR).</p> <p>METHODS AND MATERIALS: Patients aged < 30 years with high-grade NRSTS received RT (55.8 Gy) for R1 < /=5 cm tumor (arm B); RT (55.8 Gy)/CT for R0/R1 > 5 cm tumor (arm C); or neoadjuvant RT (45 Gy)/CT plus delayed surgery, CT, and postoperative boost to 10.8 Gy R0 < 5 mm margins/R1 or 19.8 Gy for R2/unresected tumors (arm D).</p> <p>RESULTS: One hundred ninety-three eligible patients had 24 LRs (arm B 1/15 [6.7%], arm C 7/65 [10.8%], arm D 16/113 [14.2%]) at median time to LR of 1.1 years (range, 0.11-5.27). Of 95 eligible for delayed surgery after neoadjuvant therapy, 89 (93.7%) achieved R0/R1 margins. Overall LC after RT were as follows: R0, 106 of 109 (97%); R1, 51 of 60 (85%); and R2/unresectable, 2 of 6 (33%). LR predictors include extent of delayed resection (P < .001), imaging response before delayed surgery (P < .001), histologic subtype (P < .001), and no RT (P = .046). The 5-year event-free survival was significantly lower (P = .0003) for patients unable to undergo R0/R1 resection.</p> <p>CONCLUSIONS: Risk-based treatment for young patients with high-grade NRSTS treated on ARST0332 produced very high LC, particularly after R0 resection (97%), despite lower-than-standard RT doses. Neoadjuvant CT/RT enabled delayed R0/R1 resection in most patients and is preferred over adjuvant therapy due to the lower RT dose delivered.</p>
dc.identifier.submissionpathfaculty_pubs/1965
dc.contributor.departmentImaging and Radiation Oncology Core (IROC)
dc.contributor.departmentDepartment of Radiation Oncology


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