Literature DB >> 20166208

Grading of nonrhabdomyosarcoma soft tissue sarcoma in children and adolescents: a comparison of parameters used for the Fédération Nationale des Centers de Lutte Contre le Cancer and Pediatric Oncology Group Systems.

Joseph D Khoury1, Cheryl M Coffin, Sheri L Spunt, James R Anderson, William H Meyer, David M Parham.   

Abstract

BACKGROUND: Two systems for grading soft tissue sarcoma are widely used currently: the National Cancer Institute (NCI) and the Fédération Nationale des Centers de Lutte Contre le Cancer (FNCLCC) systems. Both were developed using cohorts of predominantly adult patients. The Pediatric Oncology Group (POG) system, based on the NCI system, was adapted for grading pediatric nonrhabdomyosarcoma soft tissue sarcoma (NRSTS). The applicability and prognostic utility of the FNCLCC system in pediatric NRSTS has not been assessed or compared with the POG system.
METHODS: Tumors from 130 patients with malignant NRSTS enrolled on 3 completed multi-institutional clinical trials were assessed. Of 130 tumors, 102 (78%) were localized and 28 (22%) metastatic. Of the localized tumors, 55 of 102 (54%) were >5 cm. The estimated 5-year event-free survival (EFS) for the entire group was 47%.
RESULTS: As expected, stage and tumor sizes were predictive of EFS (P < .001). Both systems were predictive of 5-year EFS (POG, P = .0095 and FNCLCC, P = .0075). Patients whose tumors received discrepant grades (POG-G3 vs FNCLCC-G2/G1) (n = 44) had an intermediate outcome between those with concordant (G3 [n = 44] or G1/G2 [n = 42]) grades on both systems (P = .0018). By multivariate analysis, the mitotic index was predictive of EFS, using a cutoff of 10 mitotic figures per 10 high-power fields (P < .001).
CONCLUSIONS: In conclusion, both FNCLCC and POG systems provide an adequate prognostic measure of outcome for pediatric NRSTS; albeit, a sizeable subset of cases with apparently intermediate prognosis was graded differently by the 2 systems. The mitotic index appears to be a key parameter in grading pediatric NRSTS. (c) 2010 American Cancer Society.

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Year:  2010        PMID: 20166208      PMCID: PMC2987713          DOI: 10.1002/cncr.24929

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  21 in total

1.  Role of adjuvant chemotherapy in the treatment of surgically resected pediatric nonrhabdomyosarcomatous soft tissue sarcomas: A Pediatric Oncology Group Study.

Authors:  C B Pratt; A S Pappo; P Gieser; J J Jenkins; A Salzbergdagger; J Neff; B Rao; D Green; P Thomas; R Marcus; D Parham; H Maurer
Journal:  J Clin Oncol       Date:  1999-04       Impact factor: 44.544

2.  Predictive value of grade for metastasis development in the main histologic types of adult soft tissue sarcomas: a study of 1240 patients from the French Federation of Cancer Centers Sarcoma Group.

Authors:  J M Coindre; P Terrier; L Guillou; V Le Doussal; F Collin; D Ranchère; X Sastre; M O Vilain; F Bonichon; B N'Guyen Bui
Journal:  Cancer       Date:  2001-05-15       Impact factor: 6.860

3.  Prognostic factors for patients with localized soft-tissue sarcoma treated with conservation surgery and radiation therapy: an analysis of 1225 patients.

Authors:  Gunar K Zagars; Matthew T Ballo; Peter W T Pisters; Raphael E Pollock; Shreyaskumar R Patel; Robert S Benjamin; Harry L Evans
Journal:  Cancer       Date:  2003-05-15       Impact factor: 6.860

Review 4.  Pediatric nonrhabdomyosarcoma soft tissue sarcomas.

Authors:  Sheri L Spunt; Stephen X Skapek; Cheryl M Coffin
Journal:  Oncologist       Date:  2008-06

5.  The grading of soft tissue sarcomas. Results of a clinicohistopathologic correlation in a series of 163 cases.

Authors:  J Costa; R A Wesley; E Glatstein; S A Rosenberg
Journal:  Cancer       Date:  1984-02-01       Impact factor: 6.860

6.  Soft-tissue sarcomas of adults; study of pathological prognostic variables and definition of a histopathological grading system.

Authors:  M Trojani; G Contesso; J M Coindre; J Rouesse; N B Bui; A de Mascarel; J F Goussot; M David; F Bonichon; C Lagarde
Journal:  Int J Cancer       Date:  1984-01-15       Impact factor: 7.396

7.  The Intergroup Rhabdomyosarcoma Study-I. A final report.

Authors:  H M Maurer; M Beltangady; E A Gehan; W Crist; D Hammond; D M Hays; R Heyn; W Lawrence; W Newton; J Ortega
Journal:  Cancer       Date:  1988-01-15       Impact factor: 6.860

8.  Recurrence-free survival time for surgically treated soft tissue sarcoma patients. Multivariate analysis of five prognostic factors.

Authors:  H W Heise; M H Myers; W O Russell; H D Suit; F M Enzinger; J H Edmonson; J Cohen; R G Martin; W T Miller; S I Hajdu
Journal:  Cancer       Date:  1986-01-01       Impact factor: 6.860

Review 9.  Prognostic factors in soft tissue sarcomas. A multivariate analysis of 109 cases.

Authors:  A M Mandard; J F Petiot; J Marnay; J C Mandard; J Chasle; E de Ranieri; P Dupin; P Herlin; J de Ranieri; A Tanguy
Journal:  Cancer       Date:  1989-04-01       Impact factor: 6.860

10.  Prognostic significance of morphologic parameters in renal cell carcinoma.

Authors:  S A Fuhrman; L C Lasky; C Limas
Journal:  Am J Surg Pathol       Date:  1982-10       Impact factor: 6.394

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  8 in total

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Authors:  Anish Ray; Winston W Huh
Journal:  Curr Oncol Rep       Date:  2012-08       Impact factor: 5.075

Review 2.  [Grading of soft tissue and bone sarcomas].

Authors:  I Petersen; E Wardelmann
Journal:  Pathologe       Date:  2016-07       Impact factor: 1.011

Review 3.  Children's Oncology Group's 2013 blueprint for research: Soft tissue sarcomas.

Authors:  Douglas S Hawkins; Sheri L Spunt; Stephen X Skapek
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4.  Pediatric soft tissue sarcoma of the limbs: clinical outcome of 97 patients.

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5.  Multiple primary malignancies in elderly patients with high-grade soft tissue sarcoma.

Authors:  Eiji Kozawa; Hideshi Sugiura; Satoshi Tsukushi; Hiroshi Urakawa; Eisuke Arai; Naohisa Futamura; Hiroatsu Nakashima; Yoshihisa Yamada; Naoki Ishiguro; Yoshihiro Nishida
Journal:  Int J Clin Oncol       Date:  2013-03-20       Impact factor: 3.402

6.  A matched cohort study of radio-chemotherapy versus radiotherapy alone in soft tissue sarcoma patients.

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Journal:  Radiol Med       Date:  2018-09-12       Impact factor: 3.469

Review 7.  Overview of the clinical and imaging features of the most common non-rhabdomyosarcoma soft-tissue sarcomas.

Authors:  Simon C Kao
Journal:  Pediatr Radiol       Date:  2019-10-16

Review 8.  Malignant Peripheral Nerve Sheath Tumors-A Comprehensive Review of Pathophysiology, Diagnosis, and Multidisciplinary Management.

Authors:  Samantha W E Knight; Tristan E Knight; Teresa Santiago; Andrew J Murphy; Abdelhafeez H Abdelhafeez
Journal:  Children (Basel)       Date:  2022-01-01
  8 in total

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