Outcomes in patients with aggressive B-cell non-Hodgkin lymphoma after intensive frontline treatment failure.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
15 01 2020
Historique:
received: 07 03 2019
revised: 19 06 2019
accepted: 12 07 2019
pubmed: 1 10 2019
medline: 2 7 2020
entrez: 1 10 2019
Statut: ppublish

Résumé

Salvage immunochemotherapy followed by high-dose chemotherapy and autologous stem cell transplantation is the standard-of-care second-line treatment for patients with relapsed/refractory diffuse large B-cell lymphoma after first-line R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone). Outcomes after receipt of second-line immunochemotherapy in patients with aggressive B-cell lymphomas who relapse or are refractory to intensive first-line immunochemotherapy regimens (etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab [R-EPOCH], rituximab, hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone alternating with methotrexate and cytarabine [R-HyperCVAD], rituximab, cyclophosphamide, vincristine, doxorubicin, and high-dose methotrexate alternating with ifosfamide, etoposide, and cytarabine [R-CODOX-M/IVAC]) remain unknown. Outcomes of patients with non-Burkitt, aggressive B-cell lymphomas and relapsed/refractory disease after first-line treatment with intensive immunochemotherapy regimens who received platinum-based second-line immunochemotherapy were reviewed retrospectively. Analyses were performed to determine progression-free survival (PFS) and overall survival (OS) from the time of receipt of second-line immunochemotherapy. In total, 195 patients from 19 academic centers were included in the study. The overall response rate to second-line immunochemotherapy was 44%, with a median PFS of 3 months and a median OS of 8 months. Patients with early treatment failure (primary refractory or relapse <12 months from completion of first-line therapy) experienced inferior median PFS (2.8 vs 23 months; P < .001) and OS (6 months vs not reached; P < .001) compared with patients with late treatment failure. Although the 17% of patients with early failure who achieved a complete response to second-line immunochemotherapy experienced prolonged survival, this outcome could not be predicted by clinicopathologic features at the start of second-line immunochemotherapy. Patients with early treatment failure after intensive first-line immunochemotherapy experience poor outcomes after receiving standard second-line immunochemotherapy. The use of standard-of-care or experimental therapies currently available in the third-line setting and beyond should be investigated in the second-line setting for these patients.

Sections du résumé

BACKGROUND
Salvage immunochemotherapy followed by high-dose chemotherapy and autologous stem cell transplantation is the standard-of-care second-line treatment for patients with relapsed/refractory diffuse large B-cell lymphoma after first-line R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone). Outcomes after receipt of second-line immunochemotherapy in patients with aggressive B-cell lymphomas who relapse or are refractory to intensive first-line immunochemotherapy regimens (etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab [R-EPOCH], rituximab, hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone alternating with methotrexate and cytarabine [R-HyperCVAD], rituximab, cyclophosphamide, vincristine, doxorubicin, and high-dose methotrexate alternating with ifosfamide, etoposide, and cytarabine [R-CODOX-M/IVAC]) remain unknown.
METHODS
Outcomes of patients with non-Burkitt, aggressive B-cell lymphomas and relapsed/refractory disease after first-line treatment with intensive immunochemotherapy regimens who received platinum-based second-line immunochemotherapy were reviewed retrospectively. Analyses were performed to determine progression-free survival (PFS) and overall survival (OS) from the time of receipt of second-line immunochemotherapy.
RESULTS
In total, 195 patients from 19 academic centers were included in the study. The overall response rate to second-line immunochemotherapy was 44%, with a median PFS of 3 months and a median OS of 8 months. Patients with early treatment failure (primary refractory or relapse <12 months from completion of first-line therapy) experienced inferior median PFS (2.8 vs 23 months; P < .001) and OS (6 months vs not reached; P < .001) compared with patients with late treatment failure. Although the 17% of patients with early failure who achieved a complete response to second-line immunochemotherapy experienced prolonged survival, this outcome could not be predicted by clinicopathologic features at the start of second-line immunochemotherapy.
CONCLUSIONS
Patients with early treatment failure after intensive first-line immunochemotherapy experience poor outcomes after receiving standard second-line immunochemotherapy. The use of standard-of-care or experimental therapies currently available in the third-line setting and beyond should be investigated in the second-line setting for these patients.

Identifiants

pubmed: 31568564
doi: 10.1002/cncr.32526
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

293-303

Informations de copyright

© 2019 American Cancer Society.

Références

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Auteurs

Emily C Ayers (EC)

Abramson Cancer Center, University of Pennsylvania, Philadelphia, Pennsylvania.

Shaoying Li (S)

Department of Hematopathology, The University of Texas MD Anderson Cancer, Houston, Texas.

L Jeffrey Medeiros (LJ)

Department of Hematopathology, The University of Texas MD Anderson Cancer, Houston, Texas.

David A Bond (DA)

Department of Internal Medicine, The Ohio State University Cancer Center, Columbus, Ohio.

Kami J Maddocks (KJ)

Department of Hematology, The Ohio State University Cancer Center, Columbus, Ohio.

Pallawi Torka (P)

Roswell Park Comprehensive Cancer Center, Buffalo, New York.

Angel Mier Hicks (A)

Roswell Park Comprehensive Cancer Center, Buffalo, New York.

Madeira Curry (M)

Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland.

Nina D Wagner-Johnston (ND)

Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland.

Reem Karmali (R)

Department of Medicine, Division of Hematology/Oncology, Northwestern University Feinberg.
School of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois.

Amir Behdad (A)

Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Bita Fakhri (B)

Washington University School of Medicine, St. Louis, Missouri.

Brad S Kahl (BS)

Washington University School of Medicine, St. Louis, Missouri.

Michael C Churnetski (MC)

Department of Hematology, Winship Cancer Institute, Emory University, Atlanta, Georgia.
Department of Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia.

Jonathon B Cohen (JB)

Department of Hematology, Winship Cancer Institute, Emory University, Atlanta, Georgia.

Nishitha M Reddy (NM)

Department of Hematology/Oncology, Vanderbilt University Medical Center, Nashville, Tennessee.

Dipenkumar Modi (D)

Karmanos Cancer Institute/Wayne State University, Detroit, Michigan.

Radhakrishnan Ramchandren (R)

Hematology-Oncology, Karmanos Cancer Institute/Wayne State University, Detroit, Michigan.

Christina Howlett (C)

Deparrment of Pharmacy and Clinical Services, John Theurer Cancer Center, Hackensack Meridian Health, Hackensack, New Jersey.

Lori A Leslie (LA)

John Theurer Cancer Center, Hackensack Meridian Health, Hackensack, New Jersey.

Samuel Cytryn (S)

New York University Perlmutter Cancer Center, New York, New York.

Catherine S Diefenbach (CS)

New York University Perlmutter Cancer Center, New York, New York.

Rawan Faramand (R)

Department of Malignant Hematology, H. Lee Moffitt Cancer Center, Tampa, Florida.

Julio C Chavez (JC)

Department of Malignant Hematology, H. Lee Moffitt Cancer Center, Tampa, Florida.

Adam J Olszewski (AJ)

The Warren Alpert Medical School of Brown University, Providence, Rhode Island.
Division of Hematology-Oncology, Rhode Island Hospital, Providence, Rhode Island.

Yang Liu (Y)

Fox Chase Cancer Center, Philadelphia, Pennsylvania.

Stefan K Barta (SK)

Abramson Cancer Center, University of Pennsylvania, Philadelphia, Pennsylvania.
Fox Chase Cancer Center, Philadelphia, Pennsylvania.

Dhruvika Mukhija (D)

Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.

Brian T Hill (BT)

Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.

Helen Ma (H)

Center for Lymphoid Malignancies, Department of Medicine, and Department of Pathology and Cell Biology, Columbia University Medical Center , New York.

Jennifer E Amengual (JE)

Division of Hematology and Oncology, Department of Medicine, Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York.

Sunita Nathan (S)

Rush University Medical Center, Chicago, Illinois.

Sarit E Assouline (SE)

Medicine and Oncology, Jewish General Hospital, McGill University, Montreal, Quebec, Canada.

Victor M Orellana-Noia (VM)

University of Virginia, Charlottesville, Virginia.

Craig A Portell (CA)

Hematology and Oncology, University of Virginia, Charlottesville, Virginia.

Ashwin Chandar (A)

Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey.

Kevin A David (KA)

Rush University Medical Center, Chicago, Illinois.

Anshu Giri (A)

Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina.

Brian T Hess (BT)

Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina.

Daniel J Landsburg (DJ)

Abramson Cancer Center, University of Pennsylvania, Philadelphia, Pennsylvania.

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