Survival Outcomes of Younger Patients With Mantle Cell Lymphoma Treated in the Rituximab Era.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
20 02 2019
Historique:
pubmed: 8 1 2019
medline: 18 12 2019
entrez: 8 1 2019
Statut: ppublish

Résumé

Mantle cell lymphoma (MCL) is a B-cell lymphoma characterized by cyclin D1 expression. Autologous hematopoietic cell transplantation (AHCT) consolidation after induction chemotherapy is often used for eligible patients; however, the benefit remains uncertain in the rituximab era. Herein we retrospectively assessed the impact of AHCT consolidation on survival in a large cohort of transplantation-eligible patients age 65 years or younger. We retrospectively studied transplantation-eligible adults age 65 years or younger with newly diagnosed MCL treated between 2000 and 2015. The primary objective was to assess for improved progression-free survival (PFS) with AHCT consolidation and secondarily to assess for improved overall survival (OS). Cox multivariable regression analysis and propensity score-weighted (PSW) analysis were performed. Data were collected from 25 medical centers for 1,254 patients; 1,029 met inclusion criteria. Median follow-up for the cohort was 76 months. Median PFS and OS were 62 and 139 months, respectively. On unadjusted analysis, AHCT was associated with improved PFS (75 v 44 months with v without AHCT, respectively; P < .01) and OS (147 v 115 months with v without AHCT, respectively; P < .05). On multivariable regression analysis, AHCT was associated with improved PFS (hazard ratio [HR], 0.54; 95% CI, 0.44 to 0.66; P < .01) and a trend toward improved OS (HR, 0.77; 95% CI, 0.59 to 1.01; P = .06). After PSW analysis, AHCT remained associated with improved PFS (HR, 0.70; 95% CI, 0.59 to 0.84; P < .05) but not improved OS (HR, 0.87; 95% CI, 0.69 to 1.1; P = .2). In this large cohort of younger, transplantation-eligible patients with MCL, AHCT consolidation after induction was associated with significantly improved PFS but not OS after PSW analysis. Within the limitations of a retrospective analysis, our findings suggest that in younger, fit patients, AHCT consolidation may improve PFS.

Identifiants

pubmed: 30615550
doi: 10.1200/JCO.18.00690
pmc: PMC7554677
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Rituximab 4F4X42SYQ6

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

471-480

Subventions

Organisme : NCI NIH HHS
ID : P30 CA006927
Pays : United States

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Auteurs

James N Gerson (JN)

1 Fox Chase Cancer Center, Philadelphia, PA.

Elizabeth Handorf (E)

1 Fox Chase Cancer Center, Philadelphia, PA.

Diego Villa (D)

2 BC Cancer, Vancouver, British Columbia, Canada.

Alina S Gerrie (AS)

2 BC Cancer, Vancouver, British Columbia, Canada.

Parv Chapani (P)

2 BC Cancer, Vancouver, British Columbia, Canada.

Shaoying Li (S)

3 MD Anderson Cancer Center, Houston, TX.

L Jeffrey Medeiros (LJ)

3 MD Anderson Cancer Center, Houston, TX.

Michael I Wang (MI)

3 MD Anderson Cancer Center, Houston, TX.

Jonathon B Cohen (JB)

4 Emory University, Atlanta, GA.

Oscar Calzada (O)

4 Emory University, Atlanta, GA.

Michael C Churnetski (MC)

4 Emory University, Atlanta, GA.

Brian T Hill (BT)

5 Cleveland Clinic Foundation, Cleveland, OH.

Yazeed Sawalha (Y)

5 Cleveland Clinic Foundation, Cleveland, OH.

Francisco J Hernandez-Ilizaliturri (FJ)

6 Roswell Park Cancer Institute, Buffalo, NY.

Shalin Kothari (S)

6 Roswell Park Cancer Institute, Buffalo, NY.

Julie M Vose (JM)

7 University of Nebraska Cancer Center, Omaha, NE.

Martin A Bast (MA)

7 University of Nebraska Cancer Center, Omaha, NE.

Timothy S Fenske (TS)

8 Medical College of Wisconsin, Milwaukee, WI.

Swapna Narayana Rao Gari (S)

8 Medical College of Wisconsin, Milwaukee, WI.

Kami J Maddocks (KJ)

9 Ohio State University; Columbus, OH.

David Bond (D)

9 Ohio State University; Columbus, OH.

Veronika Bachanova (V)

10 University of Minnesota, Minneapolis, MN.

Bhaskar Kolla (B)

10 University of Minnesota, Minneapolis, MN.

Julio Chavez (J)

11 Moffitt Cancer Center, Tampa, FL.

Bijal Shah (B)

11 Moffitt Cancer Center, Tampa, FL.

Frederick Lansigan (F)

12 Dartmouth-Hitchcock Medical Center, Lebanon, NH.

Timothy F Burns (TF)

12 Dartmouth-Hitchcock Medical Center, Lebanon, NH.

Alexandra M Donovan (AM)

12 Dartmouth-Hitchcock Medical Center, Lebanon, NH.

Nina Wagner-Johnston (N)

13 Johns Hopkins University, Baltimore, MD.

Marcus Messmer (M)

13 Johns Hopkins University, Baltimore, MD.

Amitkumar Mehta (A)

14 University of Alabama Cancer Center, Birmingham, AL.

Jennifer K Anderson (JK)

14 University of Alabama Cancer Center, Birmingham, AL.

Nishitha Reddy (N)

15 Vanderbilt Ingram Cancer Center, Nashville, TN.

Alexandra E Kovach (AE)

15 Vanderbilt Ingram Cancer Center, Nashville, TN.

Daniel J Landsburg (DJ)

16 University of Pennsylvania, Philadelphia, PA.

Martha Glenn (M)

17 Huntsman Cancer Institute, Salt Lake City, UT.

David J Inwards (DJ)

18 Mayo Clinic, Rochester, MN.

Reem Karmali (R)

19 Northwestern University, Evanston, IL.

Jason B Kaplan (JB)

19 Northwestern University, Evanston, IL.

Paolo F Caimi (PF)

20 Case Western Reserve University, Cleveland, OH.

Saurabh Rajguru (S)

21 University of Wisconsin, Madison, WI.

Andrew Evens (A)

22 Tufts University, Boston, MA.

Andreas Klein (A)

22 Tufts University, Boston, MA.

Elvira Umyarova (E)

23 University of Vermont, Burlington, VT.

Bhargavi Pulluri (B)

23 University of Vermont, Burlington, VT.

Jennifer E Amengual (JE)

24 Columbia University, New York, NY.

Jennifer K Lue (JK)

24 Columbia University, New York, NY.

Catherine Diefenbach (C)

25 New York University, New York, NY.

Richard I Fisher (RI)

1 Fox Chase Cancer Center, Philadelphia, PA.

Stefan K Barta (SK)

1 Fox Chase Cancer Center, Philadelphia, PA.

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Classifications MeSH