Literature DB >> 17470866

We should desist using RECIST, at least in GIST.

Robert S Benjamin1, Haesun Choi, Homer A Macapinlac, Michael A Burgess, Shreyaskumar R Patel, Lei L Chen, Donald A Podoloff, Chuslip Charnsangavej.   

Abstract

PURPOSE: Response Evaluation Criteria in Solid Tumors (RECIST) are insensitive in evaluating imatinib-treated gastrointestinal stromal tumors (GISTs). Response by Choi criteria, a 10% decrease in size or a 15% decrease in density on contrast-enhanced CT, correlated well in a small training set of patients who showed response as measured by positron emission tomography, and was more predictive of time to tumor progression (TTP) than response by RECIST. This study was designed to validate these observations in an independent data set. PATIENTS AND METHODS: Fifty-eight patients with imatinib-treated GISTs were evaluated by RECIST and Choi criteria. TTP was compared with TTP in the training set. Patients were analyzed initially with follow-up to 28 months, extended to 60 months for survival analysis.
RESULTS: Patients who met Choi response criteria on CT at 2 months had significantly better TTP than those who did not (P = .0002), whereas response group by RECIST was not significantly correlated with TTP. Even when the 98 patients from both sets were analyzed together, the response group by RECIST did not correlate significantly with TTP, whereas response group by Choi criteria did correlate significantly with TTP. Disease-specific survival (DSS) was also significantly correlated with response group by Choi criteria (P = .04), but not with response group by RECIST.
CONCLUSION: Choi response criteria are reproducible, more sensitive, and more precise than RECIST in assessing the response of GISTs to imatinib mesylate. Response by Choi criteria, unlike response by RECIST, correlates significantly with TTP and DSS. Response by Choi criteria should be incorporated routinely into future studies of GIST therapy. We should desist using RECIST, at least in GIST.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17470866     DOI: 10.1200/JCO.2006.07.3411

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  185 in total

1.  Segmental duodenectomy for gastrointestinal stromal tumor of the duodenum.

Authors:  Nicolas Christian Buchs; Pascal Bucher; Pascal Gervaz; Sandrine Ostermann; François Pugin; Philippe Morel
Journal:  World J Gastroenterol       Date:  2010-06-14       Impact factor: 5.742

Review 2.  The use of tumour volumetrics to assess response to therapy in anticancer clinical trials.

Authors:  Gregory V Goldmacher; James Conklin
Journal:  Br J Clin Pharmacol       Date:  2012-06       Impact factor: 4.335

3.  Standardisation of liver MDCT by tracking liver parenchyma enhancement to trigger imaging.

Authors:  H Brodoefel; A Tognolini; G A Zamboni; S Gourtsoyianni; C D Claussen; V Raptopoulos
Journal:  Eur Radiol       Date:  2011-11-05       Impact factor: 5.315

4.  NCCN Task Force report: update on the management of patients with gastrointestinal stromal tumors.

Authors:  George D Demetri; Margaret von Mehren; Cristina R Antonescu; Ronald P DeMatteo; Kristen N Ganjoo; Robert G Maki; Peter W T Pisters; Chandrajit P Raut; Richard F Riedel; Scott Schuetze; Hema M Sundar; Jonathan C Trent; Jeffrey D Wayne
Journal:  J Natl Compr Canc Netw       Date:  2010-04       Impact factor: 11.908

Review 5.  Diffusion-weighted (DW) and dynamic contrast-enhanced (DCE) magnetic resonance imaging (MRI) for monitoring anticancer therapy.

Authors:  Anwar R Padhani; Aftab Alam Khan
Journal:  Target Oncol       Date:  2010-04-11       Impact factor: 4.493

Review 6.  [Implications of modern anticancer therapies for palliative care concepts].

Authors:  B Alt-Epping; F Nauck
Journal:  Schmerz       Date:  2010-12       Impact factor: 1.107

Review 7.  Moving beyond response criteria: new measures of success in the treatment of sarcomas.

Authors:  Andrew E Hendifar; Elke Ahlmann; Daniel C Allison; James Hu; Lawrence Menendez; Sant P Chawla
Journal:  Curr Treat Options Oncol       Date:  2012-09

8.  Impact of Continuing First-Line EGFR Tyrosine Kinase Inhibitor Therapy Beyond RECIST Disease Progression in Patients with Advanced EGFR-Mutated Non-Small-Cell Lung Cancer (NSCLC): Retrospective GFPC 04-13 Study.

Authors:  J B Auliac; C Fournier; C Audigier Valette; M Perol; A Bizieux; F Vinas; C Decroisette Phan van Ho; S Bota Ouchlif; R Corre; G Le Garff; P Fournel; N Baize; R Lamy; A Vergnenegre; D Arpin; B Marin; C Chouaid; R Gervais
Journal:  Target Oncol       Date:  2016-04       Impact factor: 4.493

9.  Automated tracking of quantitative assessments of tumor burden in clinical trials.

Authors:  Daniel L Rubin; Debra Willrett; Martin J O'Connor; Cleber Hage; Camille Kurtz; Dilvan A Moreira
Journal:  Transl Oncol       Date:  2014-02-01       Impact factor: 4.243

10.  Radiographic assessment and therapeutic decisions at RECIST progression in EGFR-mutant NSCLC treated with EGFR tyrosine kinase inhibitors.

Authors:  Mizuki Nishino; Stephanie Cardarella; Suzanne E Dahlberg; David M Jackman; Nikhil H Ramaiya; Hiroto Hatabu; Michael S Rabin; Pasi A Jänne; Bruce E Johnson
Journal:  Lung Cancer       Date:  2012-12-14       Impact factor: 5.705

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.