Literature DB >> 31023524

Metronomic Capecitabine With Cyclophosphamide Regimen in Unresectable or Relapsed Pseudomyxoma Peritonei.

Alessandra Raimondi1, Salvatore Corallo1, Monica Niger1, Maria Antista1, Giovanni Randon1, Federica Morano1, Massimo Milione2, Shigeki Kusamura3, Dario Baratti3, Marcello Guaglio3, Chiara Cremolini4, Federica Marmorino4, Maria Di Bartolomeo1, Marcello Deraco3, Filippo De Braud5, Filippo Pietrantonio6.   

Abstract

BACKGROUND: No standard treatment for advanced unresectable pseudomyxoma peritonei (PMP) has been defined so far. PMP is traditionally considered chemoresistant but nonrandomized series showed promising results with regimens for gastrointestinal tumors. PATIENTS AND METHODS: We conducted a single-center prospective single-arm trial. Inclusion criteria were histologically confirmed PMP, unresectable or progressive to surgery/previous treatments. Patients received a continuous metronomic regimen with capecitabine (625 mg/m2 twice per day) with cyclophosphamide (50 mg/d) until progression, unacceptable toxicity, or consent withdrawal. The primary end point was progression-free survival (PFS); secondary end points were disease control rate (DCR), overall survival (OS), and safety. Exploratory analyses were the variation of circulating tumor biomarkers and neutrophil to lymphocyte ratio (NLR).
RESULTS: Twenty-three consecutive patients were enrolled from April 2015 to October 2017. At a median follow up of 22.4 months, median PFS was 9.5 months and 1-year OS rate was 73.7%. Overall, DCR was 87% and 6 (27%) patients achieved disease control ≥12 months. The safety profile was manageable: 26% of patients reported Grade 3 drug-related adverse events and none Grade 4/5. NLR baseline < 3 versus ≥ 3 was associated with prolonged PFS (12.6 vs. 3.4 months; P = .0001).
CONCLUSION: Metronomic capecitabine with cyclophosphamide is a well tolerated regimen in unresectable/recurrent PMP, and its safety profile favorably compares with previously investigated regimens.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Capecitabine; Metronomic chemotherapy; Neutrophils-to-lymphocytes ratio; Pseudomyxoma peritonei; Systemic therapy

Mesh:

Substances:

Year:  2019        PMID: 31023524     DOI: 10.1016/j.clcc.2019.03.002

Source DB:  PubMed          Journal:  Clin Colorectal Cancer        ISSN: 1533-0028            Impact factor:   4.481


  6 in total

1.  Metronomic capecitabine as maintenance treatment after first line induction with XELOX for metastatic colorectal cancer patients.

Authors:  Rui Geng; Gang Wang; Lei Qiu; Bing Liu; Fan Yang; Jingyu Zhang; Yongchang Miao
Journal:  Medicine (Baltimore)       Date:  2020-12-18       Impact factor: 1.817

Review 2.  Role of Epithelial-Mesenchymal Plasticity in Pseudomyxoma Peritonei: Implications for Locoregional Treatments.

Authors:  Maria Luisa Calabrò; Nayana Lazzari; Giulia Rigotto; Marco Tonello; Antonio Sommariva
Journal:  Int J Mol Sci       Date:  2020-11-30       Impact factor: 5.923

Review 3.  Novel Perspectives in Pseudomyxoma Peritonei Treatment.

Authors:  Antonio Sommariva; Marco Tonello; Giulia Rigotto; Nayana Lazzari; Pierluigi Pilati; Maria Luisa Calabrò
Journal:  Cancers (Basel)       Date:  2021-11-27       Impact factor: 6.639

Review 4.  Comprehensive Understanding and Evolutional Therapeutic Schemes for Pseudomyxoma Peritonei: A Literature Review.

Authors:  Suiting Ye; Song Zheng
Journal:  Am J Clin Oncol       Date:  2022-04-14       Impact factor: 2.787

Review 5.  The role of chemotherapy in the treatment of advanced appendiceal cancers: summary of the literature and future directions.

Authors:  Madeleine C Strach; Sarah Sutherland; Lisa G Horvath; Kate Mahon
Journal:  Ther Adv Med Oncol       Date:  2022-07-23       Impact factor: 5.485

6.  Efficacy of modified FOLFOX6 chemotherapy for patients with unresectable pseudomyxoma peritonei.

Authors:  Sakura Hiraide; Keigo Komine; Yuko Sato; Kota Ouchi; Hiroo Imai; Ken Saijo; Masahiro Takahashi; Shin Takahashi; Hidekazu Shirota; Masanobu Takahashi; Chikashi Ishioka
Journal:  Int J Clin Oncol       Date:  2019-12-10       Impact factor: 3.402

  6 in total

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