scholarly journals Phase II trial of gemcitabine in patients with previously untreated metastatic cancer of the esophagus or gastroesophageal junction

2000 ◽  
Vol 11 (9) ◽  
pp. 1161-1164 ◽  
Author(s):  
A.B. Sandler ◽  
H.L. Kindler ◽  
L.H. Einhorn ◽  
E. Mitchell ◽  
G. Masters ◽  
...  
2011 ◽  
Vol 30 (4) ◽  
pp. 1684-1689 ◽  
Author(s):  
David J. Adelstein ◽  
Cristina P. Rodriguez ◽  
Lisa A. Rybicki ◽  
Denise I. Ives ◽  
Thomas W. Rice

2007 ◽  
Vol 30 (2) ◽  
pp. 172-180 ◽  
Author(s):  
David J. Adelstein ◽  
Thomas W. Rice ◽  
Lisa A. Rybicki ◽  
Jerrold P. Saxton ◽  
Gregory M. M. Videtic ◽  
...  

2006 ◽  
Vol 24 (30) ◽  
pp. 4922-4927 ◽  
Author(s):  
Tomislav Dragovich ◽  
Sheryl McCoy ◽  
Cecilia M. Fenoglio-Preiser ◽  
Jiang Wang ◽  
Jacqueline K. Benedetti ◽  
...  

Purpose A phase II trial of the oral epidermal growth factor receptor (EGFR) inhibitor erlotinib in patients with gastroesophageal adenocarcinomas stratified according to primary tumor location into two groups: gastroesophageal junction (GEJ)/cardia and distal gastric adenocarcinomas. Patients and Methods Patients with a histologically proven diagnosis of adenocarcinoma of the GEJ or stomach (ST) that was unresectable or metastatic; presence of measurable disease; no prior chemotherapy for advanced or metastatic cancer; Zubrod performance status (PS) of 0 to 1; and adequate renal, hepatic, and hematologic function were treated with erlotinib 150 mg/d orally. Patient characteristics were median age, GEJ—63 years, ST—64 years; sex, GEJ—84% male and 16% female, ST—60 male and 40 female; Zubrod PS, GEJ—25 had a PS of 0 and 18 had a PS 1, ST—13 had a PS of 0 and 12 had a PS of 1. Results Percentage of common toxicities were skin rash, 86% and 72%; fatigue, 51% and 44%; and AST/ALT elevation, 28% and 28%, respectively for GEJ and ST. There has been one confirmed complete response, three confirmed partial responses (PRs) and one unconfirmed PR for an overall response probability of 9% confirmed (95% CI, 3% to 22%), all occurring in GEJ stratum. No responses were observed in ST stratum. The median survival was 6.7 months in GEJ and 3.5 months in ST stratum. Neither intratumoral EGFR, transforming growth factor–alpha or phosphorylated Akt kinase expression nor plasma proteomic analyses were predictive of clinical outcome. No somatic mutations of the EGFR exons 18, 19, or 21 were detected and there was no gross amplification of EGFR by fluorescence in situ hybridization. Conclusion Erlotinib is active in patients with GEJ adenocarcinomas, but appears inactive in gastric cancers. The molecular correlates examined were not predictive of the patient therapeutic response.


2009 ◽  
Vol 4 (10) ◽  
pp. 1264-1269 ◽  
Author(s):  
David J. Adelstein ◽  
Thomas W. Rice ◽  
Lisa A. Rybicki ◽  
Jerrold P. Saxton ◽  
Gregory M.M. Videtic ◽  
...  

2008 ◽  
Vol 19 (1) ◽  
pp. 104-108 ◽  
Author(s):  
D. Richards ◽  
D. McCollum ◽  
L. Wilfong ◽  
M. Sborov ◽  
K.A. Boehm ◽  
...  

2009 ◽  
Vol 27 (15_suppl) ◽  
pp. e15550-e15550
Author(s):  
A. M. Horgan ◽  
G. Darling ◽  
R. Wong ◽  
A. Visbal ◽  
M. Guindi ◽  
...  

e15550 Background: Locally advanced esophageal cancer (LAEC) has a 5-year survival of < 30 %. Most patients (pts) fail after curative intent tri-modality treatment with distant metastatic disease. This phase II trial aims to determine if adjuvant targeted therapy, after neoadjuvant CRT plus surgery for resectable LAEC, may impact on systemic disease without significant toxicity. Methods: Pts with LAEC of the thoracic esophagus or gastroesophageal junction, ECOG PS 0,1 and surgical candidates treated with: preoperative Irinotecan (65mg/m2 initially, ammended to 50mg/m2) + Cisplatin (30mg/m2) on weeks 1,2,4,5,7,8 + concurrent conformal radiotherapy (50Gy/25 fractions) on weeks 4–8. Esophagectomy during weeks 15–18. Sunitinib 37.5mg daily (escalating to 50mg daily if tolerated) commenced 4–12 weeks post surgery, for 1 year. Primary endpoint is feasibility and efficacy of adjuvant sunitinib. Planned sample size 36pts. Results: 30pts enrolled from 11/06 to 12/08. Median age 64 yr (43–71), male: 22, adenocarcinoma: squamous 22:6; 10 pts stage IIA, 5 IIB and 13 III. 2 pts excluded with positive PET scan. 28 pts completed CRT - 18 pts (64%) received ≥80% of planned chemotherapy dose, 23 pts (82%) received full radiation dose. Grade 3/4 toxicity included: neutropenia (17/28), diarrhea (7/28), dehydration (4/28), febrile neutropenia (FN) (3/28) and nausea (2/28). 2 deaths on chemotherapy (1 bacterial meningitis, 1 FN) leading to irinotecan dose- reduction. Dysphagia improved in 14/23 pts during CRT. 18 pts have undergone esophagectomy. Complete pathological response in 4 (22%), downstaging in 3 (17%), stable disease in 11 (61%). 2 pts unresectable (metastases at laparotomy). 1 post-operative death due to pulmonary embolus. 9 pts have commenced sunitinib, 6 maintained at starting dose of 37.5mg; 2 dose reductions; 1 discontinued with poor wound healing. Grade 3 toxicity included: leukopenia (2/9), hand-foot reaction (1/9) and depression (1/9). Conclusions: In LAEC, induction Irinotecan/Cisplatin and radiotherapy followed by esophagectomy is associated with a significant but manageable toxicity profile. Early initiation of sunitinib is feasible and well-tolerated. Updated results to be presented. No significant financial relationships to disclose.


2002 ◽  
Vol 25 (3) ◽  
pp. 277-282 ◽  
Author(s):  
Michael Jefford ◽  
Guy C. Toner ◽  
Jennifer G. Smith ◽  
Samuel Y. K. Ngan ◽  
Danny Rischin ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document