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Salvage outcomes in patients with first relapse after fludarabine,cyclophosphamide, and rituximab for chronic lymphocytic leukemia: The French intergroup experience
Authors:Luc‐Matthieu Fornecker  Thérèse Aurran‐Schleinitz  Anne‐Sophie Michallet  Bruno Cazin  Romain Guieze  Marie‐Sarah Dilhuydy  Jean‐Marc Zini  Cécile Tomowiak  Stéphane Lepretre  Florence Cymbalista  Annie Brion  Pierre Feugier  Alain Delmer  Véronique Leblond  Loïc Ysebaert
Institution:1. Department of Hematology, H?pitaux Universitaires De Strasbourg, Strasbourg, France;2. Department of Hematology, Institut Paoli‐Calmettes, Marseille, France;3. Department of Hematology, Centre Hospitalier Lyon Sud, Hospices Civils De Lyon, Lyon, France;4. Department of Hematology, CHU, Lille, France;5. Department of Hematology, CHU De Clermont‐Ferrand, H?pital Estaing, Université Clermont 1, EA7283, CREaT, Clermont‐Ferrand, France;6. Department of Hematology, CHU, Bordeaux, France;7. Department of Hematology, H?pital Saint‐Louis, AP‐HP, Paris, France;8. Department of Hematology, CHU, Poitiers, France;9. Department of Hematology, Centre Henri Becquerel, Rouen, France;10. Department of Hematology, H?pital Avicenne, AP‐HP, Bobigny, France;11. Department of Hematology, CHU Jean Minjoz, Besan?on, France;12. Department of Hematology, CHU, Nancy, France;13. Department of Hematology, CHU, Reims, France;14. Department of Hematology, H?pital De La Pitié‐Salpétrière, AP‐HP, Paris, France;15. Department of Hematology, IUCT‐Oncopole, Toulouse, France
Abstract:The optimal management of patients with relapsed chronic lymphocytic leukemia (CLL) is dictated by the type of prior therapy, duration of prior response, presence of genomic aberrations, age, and comorbidities. The patterns of relapses and the clinical outcomes of second‐line options after fludarabine‐cyclophosphamide‐rituximab (FCR) is given as a frontline treatment are currently unknown. In this retrospective and non‐randomized study, we report the outcomes of 132 patients from databases of 14 French CLL study group centers who needed a second‐line treatment after FCR frontline. Bendamustine + rituximab (BR) was the most frequently used second‐line regimen, followed by alemtuzumab‐based regimens, R‐CHOP, and FCR. Median progression‐free survival (PFS) was 18 months after BR with a median overall survival (OS) not reached. We also found that response durations of < 36 months and the presence of del(17p) are critical factors that contribute to poor overall survival. BR appears to be an effective salvage regimen in our series, both in terms of progression‐free and overall survival. Patients who relapsed less than 36 months after FCR have a poor outcome, not significantly different in this study from patients with early relapses less than 12 or 24 months. Am. J. Hematol. 90:511–514, 2015. © 2015 Wiley Periodicals, Inc.
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