Literature DB >> 18559761

Prospective multicenter study of pegylated liposomal doxorubicin treatment in patients with advanced or refractory mycosis fungoides or Sézary syndrome.

Gaëlle Quereux1, Sonia Marques, Jean-Michel Nguyen, Christophe Bedane, Michel D'incan, Olivier Dereure, Elisabeth Puzenat, Alain Claudy, Ludovic Martin, Pascal Joly, Michele Delaunay, Marie Beylot-Barry, Pierre Vabres, Philippe Celerier, Bruno Sasolas, Florent Grange, Amir Khammari, Brigitte Dreno.   

Abstract

OBJECTIVE: To assess the rate of objective response to pegylated liposomal doxorubicin hydrochloride (Caelyx) in patients with advanced or refractory cutaneous T-cell lymphoma (CTCL).
DESIGN: Prospective, open, multicenter study.
SETTING: Thirteen dermatology departments in France. PATIENTS: Twenty-five patients with either (1) stage II to stage IV CTCL previously unsuccessfully treated with at least 2 lines of treatments or (2) histologically transformed epidermotropic CTCL requiring chemotherapy. INTERVENTION: Administration of Caelyx intravenously once every 4 weeks at a dose of 40 mg/m(2). MAIN OUTCOME MEASURES: The response to treatment was evaluated by clinical evaluation.
RESULTS: At the end of treatment, we observed an objective response (primary end point) in 56% of the patients (14 of 25): 5 complete responses and 9 partial responses. The median overall survival time was 43.7 months. For the 14 patients who experienced an objective response, the median progression-free survival time after the end of treatment was 5 months.
CONCLUSIONS: This prospective study demonstrates the effectiveness of Caelyx in treating CTCL, with an overall response rate of 56% in spite of the high proportion of patients with advanced-stage disease. Responses were observed in 2 subpopulations of patients in which the prognosis is known to be poorer: Sézary syndrome (overall response rate, 60%) and transformed CTCL (overall response rate, 50%). Moreover, this study shows that dose escalation to 40 mg/m(2) does not seem to improve the effectiveness but increases toxic effects (especially hematologic toxic effects) compared with the dose previously tested of 20 mg/m(2).

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Year:  2008        PMID: 18559761     DOI: 10.1001/archderm.144.6.727

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  14 in total

Review 1.  [Treatment of mycosis fungoides and Sézary syndrome].

Authors:  J P Nicolay; C Assaf
Journal:  Hautarzt       Date:  2017-09       Impact factor: 0.751

Review 2.  Mycosis Fungoides and Sézary Syndrome: An Update.

Authors:  Cecilia Larocca; Thomas Kupper
Journal:  Hematol Oncol Clin North Am       Date:  2019-02       Impact factor: 3.722

3.  [Management of cutaneous lymphomas].

Authors:  J P Nicolay; C-D Klemke
Journal:  Hautarzt       Date:  2014-07       Impact factor: 0.751

4.  Pharmacodynamic and pharmacokinetic study of pegylated liposomal doxorubicin combination (CCOP) chemotherapy in patients with peripheral T-cell lymphomas.

Authors:  Yun Fan; Neng-ming Lin; Lü-hong Luo; Luo Fang; Zhi-yu Huang; Hai-feng Yu; Feng-qin Wu
Journal:  Acta Pharmacol Sin       Date:  2011-03       Impact factor: 6.150

5.  How we treat mycosis fungoides and Sézary syndrome.

Authors:  Niloufer Khan; Sarah J Noor; Steven Horwitz
Journal:  Clin Adv Hematol Oncol       Date:  2021-09

6.  Cutaneous T-cell lymphoma in sub-Saharan Africa.

Authors:  Matthew Ulrickson; Fred Okuku; Victoria Walusansa; Oliver Press; Sam Kalungi; David Wu; Fred Kambugu; Corey Casper; Jackson Orem
Journal:  J Natl Compr Canc Netw       Date:  2013-03-01       Impact factor: 11.908

Review 7.  Cutaneous T-cell lymphoma: 2016 update on diagnosis, risk-stratification, and management.

Authors:  Ryan A Wilcox
Journal:  Am J Hematol       Date:  2015-11-26       Impact factor: 10.047

Review 8.  Mycosis Fungoides and Sézary Syndrome: Updates and Review of Current Therapy.

Authors:  Hiroaki Kamijo; Tomomitsu Miyagaki
Journal:  Curr Treat Options Oncol       Date:  2021-01-07

9.  Xenograft and cell culture models of Sézary syndrome reveal cell of origin diversity and subclonal heterogeneity.

Authors:  Martina Prochazkova-Carlotti; Floriane Cherrier; Audrey Gros; Sandrine Poglio; Elodie Laharanne; Anne Pham-Ledard; Marie Beylot-Barry; Jean-Philippe Merlio
Journal:  Leukemia       Date:  2020-10-26       Impact factor: 11.528

10.  Phase II study of gemcitabine and bexarotene (GEMBEX) in the treatment of cutaneous T-cell lymphoma.

Authors:  T Illidge; C Chan; N Counsell; S Morris; J Scarisbrick; D Gilson; B Popova; P Patrick; P Smith; S Whittaker; R Cowan
Journal:  Br J Cancer       Date:  2013-10-17       Impact factor: 7.640

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