Literature DB >> 33512054

Activity of Sorafenib Plus Capecitabine in Previously Treated Metastatic Colorectal Cancer.

Thomas J George1,2, Alison M Ivey2, Azka Ali1,2, Ji-Hyun Lee3,4, Yu Wang4, Karen C Daily1,2, Brian H Ramnaraign1,2, Sanda A Tan5, Krista P Terracina5, Thomas E Read5, Long H Dang6, Atif Iqbal7,8.   

Abstract

LESSONS LEARNED: Treatment for patients with metastatic colorectal cancer (mCRC) typically involves multiple lines of therapy with eventual development of treatment resistance. In this single-arm, phase II study involving heavily pretreated patients, the combination of sorafenib and capecitabine yielded a clinically meaningful progression-free survival of 6.2 months with an acceptable toxicity profile. This oral doublet therapy is worthy of continued investigation for clinical use in patients with mCRC.
BACKGROUND: Capecitabine (Cape) is an oral prodrug of the antimetabolite 5-fluorouracil. Sorafenib (Sor) inhibits multiple signaling pathways involved in angiogenesis and tumor proliferation. SorCape has been previously studied in metastatic breast cancer.
METHODS: This single-arm, phase II study was designed to evaluate the activity of SorCape in refractory metastatic colorectal cancer (mCRC). Patients received Sor (200 mg p.o. b.i.d. max daily) and Cape (1,000 mg/m2 p.o. b.i.d. on days 1-14) on a 21-day treatment cycle. Primary endpoint was progression-free survival (PFS) with preplanned comparison with historical controls.
RESULTS: Forty-two patients were treated for a median number of 3.5 cycles (range 1-39). Median PFS was 6.2 (95% confidence interval [CI], 4.3-7.9) months, and overall survival (OS) was 8.8 (95% CI, 4.3-12.2) months. One patient (2.4%) had partial response (PR), and 22 patients (52.4%) had stable disease (SD) for a clinical benefit rate of 54.8% (95% CI, 38.7%-70.2%). Hand-foot syndrome was the most common adverse event seen in 36 patients (85.7%) and was grade ≥ 3 in 16 patients (38.1%). One patient (2.4%) had a grade 4 sepsis, and one patient (2.4%) died while on treatment.
CONCLUSION: SorCape in this heavily pretreated population yielded a reasonable PFS with manageable but notable toxicity. The combination should be investigated further. © AlphaMed Press; the data published online to support this summary are the property of the authors.

Entities:  

Keywords:  Capecitabine; Colorectal cancer; Metastatic cancer; Oral therapy; Sorafenib

Mesh:

Substances:

Year:  2021        PMID: 33512054      PMCID: PMC8100547          DOI: 10.1002/onco.13689

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  16 in total

1.  Phase I clinical and pharmacokinetic study of the Novel Raf kinase and vascular endothelial growth factor receptor inhibitor BAY 43-9006 in patients with advanced refractory solid tumors.

Authors:  Dirk Strumberg; Heike Richly; Ralf A Hilger; Norbert Schleucher; Sonke Korfee; Mitra Tewes; Markus Faghih; Erich Brendel; Dimitris Voliotis; Claus G Haase; Brian Schwartz; Ahmad Awada; Rudolf Voigtmann; Max E Scheulen; Siegfried Seeber
Journal:  J Clin Oncol       Date:  2004-12-21       Impact factor: 44.544

2.  Phase I study to determine the safety and pharmacokinetics of the novel Raf kinase and VEGFR inhibitor BAY 43-9006, administered for 28 days on/7 days off in patients with advanced, refractory solid tumors.

Authors:  M Moore; H W Hirte; L Siu; A Oza; S J Hotte; O Petrenciuc; F Cihon; C Lathia; B Schwartz
Journal:  Ann Oncol       Date:  2005-07-08       Impact factor: 32.976

3.  Results of a Phase I trial of sorafenib (BAY 43-9006) in combination with doxorubicin in patients with refractory solid tumors.

Authors:  H Richly; B F Henning; P Kupsch; K Passarge; M Grubert; R A Hilger; O Christensen; E Brendel; B Schwartz; M Ludwig; C Flashar; R Voigtmann; M E Scheulen; S Seeber; D Strumberg
Journal:  Ann Oncol       Date:  2006-02-24       Impact factor: 32.976

4.  Salvage treatment with single-agent capecitabine in patients with heavily pretreated advanced colorectal cancer.

Authors:  Alexandros S Ardavanis; Georgios N Ioannidis; George S Orphanos; Gerassimos A Rigatos
Journal:  Anticancer Res       Date:  2006 Mar-Apr       Impact factor: 2.480

5.  Safety and pharmacokinetics of the dual action Raf kinase and vascular endothelial growth factor receptor inhibitor, BAY 43-9006, in patients with advanced, refractory solid tumors.

Authors:  Jeffrey W Clark; Joseph P Eder; David Ryan; Chetan Lathia; Heinz-Josef Lenz
Journal:  Clin Cancer Res       Date:  2005-08-01       Impact factor: 12.531

6.  Single-agent capecitabine in patients with metastatic colorectal cancer refractory to 5-fluorouracil/leucovorin chemotherapy.

Authors:  Jae Jin Lee; Tae Min Kim; Su Jong Yu; Dong-Wan Kim; Yo-han Joh; Do-Youn Oh; Jung Hye Kwon; Tae You Kim; Dae Seog Heo; Yung-Jue Bang; Noe Kyeong Kim
Journal:  Jpn J Clin Oncol       Date:  2004-07       Impact factor: 3.019

7.  Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer.

Authors:  Herbert Hurwitz; Louis Fehrenbacher; William Novotny; Thomas Cartwright; John Hainsworth; William Heim; Jordan Berlin; Ari Baron; Susan Griffing; Eric Holmgren; Napoleone Ferrara; Gwen Fyfe; Beth Rogers; Robert Ross; Fairooz Kabbinavar
Journal:  N Engl J Med       Date:  2004-06-03       Impact factor: 91.245

8.  Randomized, controlled trial of irinotecan plus infusional, bolus, or oral fluoropyrimidines in first-line treatment of metastatic colorectal cancer: results from the BICC-C Study.

Authors:  Charles S Fuchs; John Marshall; Edith Mitchell; Rafal Wierzbicki; Vinod Ganju; Mark Jeffery; Joseph Schulz; Donald Richards; Raoudha Soufi-Mahjoubi; Benjamin Wang; José Barrueco
Journal:  J Clin Oncol       Date:  2007-10-20       Impact factor: 44.544

9.  Bevacizumab in combination with oxaliplatin, fluorouracil, and leucovorin (FOLFOX4) for previously treated metastatic colorectal cancer: results from the Eastern Cooperative Oncology Group Study E3200.

Authors:  Bruce J Giantonio; Paul J Catalano; Neal J Meropol; Peter J O'Dwyer; Edith P Mitchell; Steven R Alberts; Michael A Schwartz; Al B Benson
Journal:  J Clin Oncol       Date:  2007-04-20       Impact factor: 44.544

10.  Phase I safety and pharmacokinetics of BAY 43-9006 administered for 21 days on/7 days off in patients with advanced, refractory solid tumours.

Authors:  A Awada; A Hendlisz; T Gil; S Bartholomeus; M Mano; D de Valeriola; D Strumberg; E Brendel; C G Haase; B Schwartz; M Piccart
Journal:  Br J Cancer       Date:  2005-05-23       Impact factor: 7.640

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