Literature DB >> 32012255

Relationship between tumor response at therapy completion and prognosis in patients with Group III rhabdomyosarcoma: A report from the Children's Oncology Group.

Timothy B Lautz1, Yueh-Yun Chi2, Jing Tian2, Abha A Gupta3, Suzanne L Wolden4, Jonathan C Routh5, Dana L Casey4, Roshni Dasgupta6, Douglas S Hawkins7, David A Rodeberg8.   

Abstract

A subset of patients with initially unresected (Clinical Group III) rhabdomyosarcoma achieve less than a complete response (CR) despite multimodal therapy. We assessed outcome based upon tumor response at the completion of all planned therapy. We studied 601 Clinical Group III participants who completed all protocol therapy without developing progressive disease on two Children's Oncology Group studies ARST0531 (n = 285) and D9803 (n = 316). Response was defined by imaging and categorized by response; complete resolution (CR), partial response (PR) or no response (NR). Failure-free survival (FFS) and overall survival (OS) between response groups were compared using the log-rank test. We found that radiographic response was CR in 393 (65.4%) and PR/NR in 208 (34.6%) patients. Achieving CR status was associated with study D9803, nonparameningeal (PM) primary sites, tumors ≤5 cm, noninvasive tumors and alveolar histology/FOXO fusion-positive tumors. The overall 5-year FFS was 75% for those achieving CR and 66.5% in those with PR/NR (adj. p = 0.094). Patients with PM primary site who achieved CR had significantly improved FFS (adj. p = 0.037) while those with non-PM primary sites had similar outcomes (adj. p = 0.47). Radiographic response was not associated with OS (adj. p = 0.21). Resection of the end-of-therapy mass did not improve FFS (p = 0.12) or OS (p = 0.37). In conclusion, CR status at the end of protocol therapy in patients with PM Clinical Group III RMS was associated with improved FFS but not OS. Efforts to understand the biology and treatment response in patients with PM primary site are under investigation.
© 2020 UICC.

Entities:  

Keywords:  paramengineal; residual mass; rhabdomyosarcoma

Mesh:

Year:  2020        PMID: 32012255      PMCID: PMC7771199          DOI: 10.1002/ijc.32896

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  21 in total

1.  Impact of tumor viability at second-look procedures performed before completing treatment on the Intergroup Rhabdomyosarcoma Study Group protocol IRS-IV, 1991-1997: a report from the children's oncology group.

Authors:  Beverly Raney; Julie Stoner; James Anderson; Richard Andrassy; Carola Arndt; Ken Brown; William Crist; Harold Maurer; Stephen Qualman; Moody Wharam; Eugene Wiener; William Meyer; Andrea Hayes-Jordan
Journal:  J Pediatr Surg       Date:  2010-11       Impact factor: 2.545

2.  Delayed primary excision with subsequent modification of radiotherapy dose for intermediate-risk rhabdomyosarcoma: a report from the Children's Oncology Group Soft Tissue Sarcoma Committee.

Authors:  David A Rodeberg; Moody D Wharam; Elizabeth R Lyden; Julie A Stoner; Kenneth Brown; Suzanne L Wolden; Charles N Paidas; Sarah S Donaldson; Douglas S Hawkins; Sheri L Spunt; Carola A Arndt
Journal:  Int J Cancer       Date:  2014-12-10       Impact factor: 7.396

3.  The prognostic value of early radiographic response in children and adolescents with embryonal rhabdomyosarcoma stage IV, metastases confined to the lungs: A report from the Cooperative Weichteilsarkom Studiengruppe (CWS).

Authors:  Monika Sparber-Sauer; Thekla von Kalle; Guido Seitz; Tobias Dantonello; Monika Scheer; Marc Münter; Joerg Fuchs; Ruth Ladenstein; Stefan S Bielack; Thomas Klingebiel; Ewa Koscielniak
Journal:  Pediatr Blood Cancer       Date:  2017-03-17       Impact factor: 3.167

4.  Vincristine, actinomycin, and cyclophosphamide compared with vincristine, actinomycin, and cyclophosphamide alternating with vincristine, topotecan, and cyclophosphamide for intermediate-risk rhabdomyosarcoma: children's oncology group study D9803.

Authors:  Carola A S Arndt; Julie A Stoner; Douglas S Hawkins; David A Rodeberg; Andrea A Hayes-Jordan; Charles N Paidas; David M Parham; Lisa A Teot; Moody D Wharam; John C Breneman; Sarah S Donaldson; James R Anderson; William H Meyer
Journal:  J Clin Oncol       Date:  2009-09-21       Impact factor: 44.544

5.  Treatment of non-metastatic rhabdomyosarcomas in childhood and adolescence. Results of the second study of the International Society of Paediatric Oncology: MMT84.

Authors:  F Flamant; C Rodary; A Rey; M T Praquin; D Sommelet; E Quintana; S Theobald; M Brunat-Mentigny; J Otten; P A Voûte; J L Habrand; H Martelli; A Barrett; M J Terrier-Lacombe; O Oberlin
Journal:  Eur J Cancer       Date:  1998-06       Impact factor: 9.162

6.  Early response as assessed by anatomic imaging does not predict failure-free survival among patients with Group III rhabdomyosarcoma: a report from the Children's Oncology Group.

Authors:  Abby R Rosenberg; James R Anderson; Elizabeth Lyden; David A Rodeberg; Suzanne L Wolden; Simon C Kao; David M Parham; Carola Arndt; Douglas S Hawkins
Journal:  Eur J Cancer       Date:  2013-12-18       Impact factor: 9.162

7.  Prognostic significance of tumor response at the end of therapy in group III rhabdomyosarcoma: a report from the children's oncology group.

Authors:  David A Rodeberg; Julie A Stoner; Andrea Hayes-Jordan; Simon C Kao; Suzanne L Wolden; Steve J Qualman; William H Meyer; Douglas S Hawkins
Journal:  J Clin Oncol       Date:  2009-05-26       Impact factor: 44.544

8.  Assessment of response to induction therapy and its influence on 5-year failure-free survival in group III rhabdomyosarcoma: the Intergroup Rhabdomyosarcoma Study-IV experience--a report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group.

Authors:  Megan Burke; James R Anderson; Simon C Kao; David Rodeberg; Stephen J Qualman; Suzanne L Wolden; William H Meyer; Philip P Breitfeld
Journal:  J Clin Oncol       Date:  2007-11-01       Impact factor: 44.544

9.  MYOD1-mutant spindle cell and sclerosing rhabdomyosarcoma: an aggressive subtype irrespective of age. A reappraisal for molecular classification and risk stratification.

Authors:  Narasimhan P Agaram; Michael P LaQuaglia; Rita Alaggio; Lei Zhang; Yumi Fujisawa; Marc Ladanyi; Leonard H Wexler; Cristina R Antonescu
Journal:  Mod Pathol       Date:  2018-09-04       Impact factor: 7.842

10.  MYOD1 (L122R) mutations are associated with spindle cell and sclerosing rhabdomyosarcomas with aggressive clinical outcomes.

Authors:  Bharat Rekhi; Pawan Upadhyay; Manoj P Ramteke; Amit Dutt
Journal:  Mod Pathol       Date:  2016-08-26       Impact factor: 7.842

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  3 in total

1.  Radiation therapy is an important factor to improve survival in pediatric patients with head and neck rhabdomyosarcoma by enhancing local control: a historical cohort study from a single center.

Authors:  Yuan Wen; Dongsheng Huang; Weiling Zhang; Yi Zhang; Huimin Hu; Jing Li
Journal:  BMC Pediatr       Date:  2020-05-29       Impact factor: 2.125

2.  Persistent mass after treatment for orbital rhabdomyosarcoma.

Authors:  Jonathan C Siktberg; Alexandra E Kovach; Scott C Borinstein; Hernan Correa; Frank W Virgin; Rachel K Sobel
Journal:  Am J Ophthalmol Case Rep       Date:  2022-01-20

3.  European guideline for imaging in paediatric and adolescent rhabdomyosarcoma - joint statement by the European Paediatric Soft Tissue Sarcoma Study Group, the Cooperative Weichteilsarkom Studiengruppe and the Oncology Task Force of the European Society of Paediatric Radiology.

Authors:  Roelof van Ewijk; Reineke A Schoot; Monika Sparber-Sauer; Simone A J Ter Horst; Nina Jehanno; Lise Borgwardt; Bart de Keizer; Johannes H M Merks; Alberto de Luca; Kieran McHugh; Thekla von Kalle; Jürgen F Schäfer; Rick R van Rijn
Journal:  Pediatr Radiol       Date:  2021-06-17
  3 in total

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