Literature DB >> 26438119

Randomized Multicenter Phase II Study of Modified Docetaxel, Cisplatin, and Fluorouracil (DCF) Versus DCF Plus Growth Factor Support in Patients With Metastatic Gastric Adenocarcinoma: A Study of the US Gastric Cancer Consortium.

Manish A Shah, Yelena Y Janjigian, Ronald Stoller, Stephen Shibata, Margaret Kemeny, Smitha Krishnamurthi, Yungpo Bernard Su, Allyson Ocean, Marinela Capanu, Bhoomi Mehrotra, Paul Ritch, Charles Henderson, David P Kelsen.   

Abstract

PURPOSE: Docetaxel, cisplatin, and fluorouracil (DCF) is a standard first-line three-drug chemotherapy regimen for advanced gastric or gastroesophageal junction (GEJ) adenocarcinoma and is associated with significant toxicity. We examined the safety and efficacy of a modified DCF (mDCF) regimen in a randomized multicenter phase II study. PATIENTS AND METHODS: Previously untreated patients with metastatic gastric or GEJ adenocarcinoma were randomly assigned to receive either mDCF (fluorouracil 2,000 mg/m2 intravenously [IV] over 48 hours, docetaxel 40 mg/m2 IV on day 1, cisplatin 40 mg/m2 IV on day 3, every 2 weeks) or parent DCF (docetaxel 75 mg/m2, cisplatin 75 mg/m2, and fluorouracil 750 mg/m2 IV over 5 days with granulocyte colony-stimulating factor, every 3 weeks). The study had 90% power to differentiate between 6-month progression-free survival of 26% and 43%, with type I and II error rates of 10% each. An early stopping rule for toxicity was included, defined as grade 3 to 4 adverse event rate > 70% in the first 3 months.
RESULTS: From November 2006 to June 2010, 85 evaluable patients were enrolled (male, n = 61; female, n = 24; median age, 58 years; Karnofsky performance status, 90%; GEJ, n = 28; gastric, 57). mDCF (n = 54) toxicity rates included 54% grade 3 to 4 toxicity (22% hospitalized) within the first 3 months and 76% grade 3 to 4 toxicity over the course of treatment. The DCF arm (n = 31) closed early because of toxicity, with rates of 71% grade 3 to 4 toxicity (52% hospitalized) within 3 months and 90% grade 3 to 4 toxicity over the course of treatment. Six-month PFS was 63% (95% CI, 48% to 75%) for mDCF and 53% (95% CI, 34% to 69%) for DCF. Median overall survival was improved for mDCF (18.8 v 12.6 months; P = .007).
CONCLUSION: mDCF is less toxic than parent DCF, even when supported with growth factors, and is associated with improved efficacy. mDCF should be considered a standard first-line option for patients with metastatic gastric or GEJ adenocarcinoma.

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Year:  2015        PMID: 26438119     DOI: 10.1200/JCO.2015.60.7465

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


  53 in total

1.  mDCF--new standard-of-care?

Authors:  Diana Romero
Journal:  Nat Rev Clin Oncol       Date:  2015-10-20       Impact factor: 66.675

2.  Modified Docetaxel, Cisplatin, and Fluorouracil (mDCF) as a Neoadjuvant Chemotherapy for Non-metastatic Esophageal Cancer (nMEC).

Authors:  Adedayo A Onitilo; Trista J Stankowski-Drengler; Oyewale Shiyanbola; Jessica Engel; Sabo Tanimu; Seth O Fagbemi; Ya-Huei Li
Journal:  Clin Med Res       Date:  2021-03-31

Review 3.  Palliative chemotherapy and targeted therapies for esophageal and gastroesophageal junction cancer.

Authors:  Vincent T Janmaat; Ewout W Steyerberg; Ate van der Gaast; Ron Hj Mathijssen; Marco J Bruno; Maikel P Peppelenbosch; Ernst J Kuipers; Manon Cw Spaander
Journal:  Cochrane Database Syst Rev       Date:  2017-11-28

4.  Surgical Outcome and Long-Term Survival of Conversion Surgery for Advanced Gastric Cancer.

Authors:  Guo-Ming Chen; Shu-Qiang Yuan; Run-Cong Nie; Tian-Qi Luo; Kai-Ming Jiang; Cheng-Cai Liang; Yuan-Fang Li; De-Yao Zhang; Jie-Hai Yu; Fan Hou; Yun Wang; Ying-Bo Chen
Journal:  Ann Surg Oncol       Date:  2020-06-06       Impact factor: 5.344

5.  FOLFCIS Treatment and Genomic Correlates of Response in Advanced Anal Squamous Cell Cancer.

Authors:  Sebastian Mondaca; Walid K Chatila; David Bates; Jaclyn F Hechtman; Andrea Cercek; Neil H Segal; Zsofia K Stadler; Anna M Varghese; Ritika Kundra; Marinela Capanu; Jinru Shia; Nikolaus Schultz; Leonard Saltz; Rona Yaeger
Journal:  Clin Colorectal Cancer       Date:  2018-09-21       Impact factor: 4.481

6.  Clinical effectiveness and toxicity of second-line irinotecan in advanced gastric and gastroesophageal junction adenocarcinoma: a single-center observational study.

Authors:  Sebastian Ochenduszko; Mirosława Puskulluoglu; Kamil Konopka; Kamil Fijorek; Agnieszka Julia Slowik; Michał Pędziwiatr; Andrzej Budzyński
Journal:  Ther Adv Med Oncol       Date:  2017-02-07       Impact factor: 8.168

Review 7.  Current therapeutic landscape for advanced gastroesophageal cancers.

Authors:  Anthony Lopez; Kazuto Harada; Dilsa Mizrak Kaya; Jaffer A Ajani
Journal:  Ann Transl Med       Date:  2018-02

8.  FOLFIRINOX for the Treatment of Advanced Gastroesophageal Cancers: A Phase 2 Nonrandomized Clinical Trial.

Authors:  Haeseong Park; Ramon U Jin; Andrea Wang-Gillam; Rama Suresh; Caron Rigden; Manik Amin; Benjamin R Tan; Katrina S Pedersen; Kian-Huat Lim; Nikolaos A Trikalinos; Abhilasha Acharya; Megan L Copsey; Katherine A Navo; Ashley E Morton; Feng Gao; A Craig Lockhart
Journal:  JAMA Oncol       Date:  2020-08-01       Impact factor: 31.777

9.  Phase II study of oxaliplatin, irinotecan and S-1 therapy in patients with advanced gastric cancer: the Korean Cancer Study Group ST14-11.

Authors:  Hyeong Su Kim; Min-Hee Ryu; Dae Young Zang; Sook Ryun Park; Boram Han; Won Ki Kang; Sun Young Rha; Minkyu Jung; Jin-Soo Kim; Byung Woog Kang; Kyung-Hee Lee; Sang-Young Rho; Jung Han Kim; Kab Choong Kim; Ji Woong Cho; Dae Ro Choi; Hyun Lim; Ho Suk Kang; Jae Seung Soh; Min-Jeong Kim; Jinwon Seo; Yoon-Koo Kang
Journal:  Gastric Cancer       Date:  2018-01-25       Impact factor: 7.370

10.  RAD51B as a potential biomarker for early detection and poor prognostic evaluation contributes to tumorigenesis of gastric cancer.

Authors:  Yikun Cheng; Bin Yang; Yanfeng Xi; Xing Chen
Journal:  Tumour Biol       Date:  2016-09-20
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