Literature DB >> 29211298

Prognostic relevance of early radiologic response to induction chemotherapy in pediatric rhabdomyosarcoma: A report from the International Society of Pediatric Oncology Malignant Mesenchymal Tumor 95 study.

Bas Vaarwerk1, Johanna H van der Lee2, Willemijn B Breunis1, Daniel Orbach3, Julia C Chisholm4, Nathalie Cozic5, Meriel Jenney6, Rick R van Rijn7, Kieran McHugh8, Soledad Gallego9, Heidi Glosli10, Christine Devalck11, Mark N Gaze12, Anna Kelsey13, Christophe Bergeron14, Michael C G Stevens15, Odile Oberlin16, Veronique Minard-Colin16, Johannes H M Merks1.   

Abstract

BACKGROUND: Early response to induction chemotherapy is used in current European guidelines to evaluate the efficacy of chemotherapy and subsequently to adapt treatment in pediatric patients with rhabdomyosarcoma (RMS). However, existing literature on the prognostic value of early radiologic response on survival is contradictory; here the prognostic value is analyzed with data from the International Society of Pediatric Oncology (SIOP) Malignant Mesenchymal Tumor 95 (MMT-95) study.
METHODS: This study examined 432 Intergroup Rhabdomyosarcoma Study Grouping III (macroscopic residue) patients enrolled in the SIOP MMT-95 study with a response assessment after 3 courses of chemotherapy (a 2-dimensional assessment). Patients with progressive disease (PD) after 3 courses of chemotherapy were excluded (n = 7). Failure-free survival (FFS) and overall survival (OS), calculated with the Kaplan-Meier method, were compared for 3 groups (complete response [CR]/partial response [PR], objective response [OR], and no response [NR]). The prognostic impact of early response was assessed through the calculation of Cox proportional hazards.
RESULTS: After 3 courses of chemotherapy, 85.2% of the patients had CR/PR, 8.6% had OR, and 6.3% had NR. For all patients, the 5-year FFS and OS rates were 60% (95% confidence interval [CI], 56%-65%) and 74% (95% CI, 70%-78%), respectively. However, a Cox proportional hazards regression analysis revealed no significant difference in FFS or OS between the response groups. The adjusted hazard ratios for an OR and NR were 1.09 (95% CI, 0.63-1.88) and 0.81 (95% CI, 0.39-1.67), respectively, for FFS and 0.91 (95% CI, 0.47-1.76) and 1.27 (95% CI, 0.61-2.64), respectively, for OS.
CONCLUSIONS: No evidence was found for the idea that early radiologic response to chemotherapy is prognostic for survival for patients with RMS. Treatment adaptation based on early response (except for patients with PD) should, therefore, no longer be incorporated into future studies. Cancer 2018;124:1016-24.
© 2017 American Cancer Society. © 2017 American Cancer Society.

Entities:  

Keywords:  chemotherapy; pediatric cancer; prognosis; rhabdomyosarcoma; tumor response

Mesh:

Year:  2017        PMID: 29211298     DOI: 10.1002/cncr.31157

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


  7 in total

1.  Evaluation of clinical efficacy of Chemotherapy for Rhabdomyosarcoma in children.

Authors:  Zhaohui Ning; Xiping Liu; Guang Qin; Lei Wei; Xia Li; Jingjing Shen
Journal:  Pak J Med Sci       Date:  2020 Jul-Aug       Impact factor: 1.088

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

Authors:  Timothy B Lautz; Yueh-Yun Chi; Jing Tian; Abha A Gupta; Suzanne L Wolden; Jonathan C Routh; Dana L Casey; Roshni Dasgupta; Douglas S Hawkins; David A Rodeberg
Journal:  Int J Cancer       Date:  2020-02-15       Impact factor: 7.396

Review 3.  European Society of Paediatric Radiology 2019 strategic research agenda: improving imaging for tomorrow's children.

Authors:  Owen J Arthurs; Rick R van Rijn; Claudio Granata; Luciana Porto; F Wolfgang Hirsch; Karen Rosendahl
Journal:  Pediatr Radiol       Date:  2019-05-21

4.  Metabolic response as assessed by 18 F-fluorodeoxyglucose positron emission tomography-computed tomography does not predict outcome in patients with intermediate- or high-risk rhabdomyosarcoma: A report from the Children's Oncology Group Soft Tissue Sarcoma Committee.

Authors:  Douglas J Harrison; Yueh-Yun Chi; Jing Tian; Pooja Hingorani; Leo Mascarenhas; Geoffrey B McCowage; Brenda J Weigel; Rajkumar Venkatramani; Suzanne L Wolden; Torunn I Yock; David A Rodeberg; Andrea A Hayes-Jordan; Lisa A Teot; Sheri L Spunt; William H Meyer; Douglas S Hawkins; Barry L Shulkin; Marguerite T Parisi
Journal:  Cancer Med       Date:  2020-12-19       Impact factor: 4.452

5.  Approaches to identifying drug resistance mechanisms to clinically relevant treatments in childhood rhabdomyosarcoma.

Authors:  Samson Ghilu; Christopher L Morton; Angelina V Vaseva; Siyuan Zheng; Raushan T Kurmasheva; Peter J Houghton
Journal:  Cancer Drug Resist       Date:  2022-01-04

6.  An evolutionary framework for treating pediatric sarcomas.

Authors:  Damon R Reed; Jonathan Metts; Mariyah Pressley; Brooke L Fridley; Masanori Hayashi; Michael S Isakoff; David M Loeb; Rikesh Makanji; Ryan D Roberts; Matteo Trucco; Lars M Wagner; Mark G Alexandrow; Robert A Gatenby; Joel S Brown
Journal:  Cancer       Date:  2020-03-16       Impact factor: 6.860

7.  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
  7 in total

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