Outcomes Among Classical Hodgkin Lymphoma Patients After an Interim PET Scan: A Real-World Experience.


Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
07 2022
Historique:
received: 21 09 2021
revised: 17 11 2021
accepted: 18 12 2021
pubmed: 31 1 2022
medline: 22 6 2022
entrez: 30 1 2022
Statut: ppublish

Résumé

The utility of dose escalation after positive positron emission tomography following 2 cycles of ABVD (PET2) for Hodgkin Lymphoma (HL) remains controversial. We describe the United States real-world practice patterns for PET2 positive patients. Data was collected from 15 sites on PET2 positive HL patients after receiving frontline treatment between January, 2015 and June, 2019. Descriptive analyses between those with therapy change and those continuing initial therapy were assessed. A total of 129 patients were identified; 111 (86%) were treated with ABVD therapy and 18 (14%) with an alternate regimen. At PET2 assessment, 74.4% (96/129) had Deauville score (DS) 4 and 25.6% (33/129) had DS 5. Of the 66 limited stage (LS) patients with PET2 DS score of 4/5, 77.3% (51/66) continued initial therapy and 22.7% (15/66) changed to escalated therapy. The 12-month progression-free survival (PFS) for DS 4/5 LS patients was 67.0% (95% CI; 54.9-81.7) for patients without escalation compared with 51.4% (95% CI; 30.8-85.8) for those who escalated. Of the 63 DS 4/5 patients with advanced stage (AS) disease, 76.2% (48/63) continued initial therapy and 23.8% (15/63) changed to escalated therapy. The 12-month PFS for DS 4/5 AS patients was 38.3% (95% CI: 26.3%-55.7%) for patients without escalation compared with 57.1% (95% CI: 36.3-89.9) for those with escalation. A minority of PET2 positive HL patients undergo therapy escalation and outcomes remain overall suboptimal. Improved prognostics markers and better therapeutics are required to improve outcomes for high-risk PET2 positive HL patients.

Identifiants

pubmed: 35093285
pii: S2152-2650(21)02483-6
doi: 10.1016/j.clml.2021.12.012
pii:
doi:

Substances chimiques

Bleomycin 11056-06-7
Vinblastine 5V9KLZ54CY
Dacarbazine 7GR28W0FJI
Doxorubicin 80168379AG

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e435-e442

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Muhammad Saad Hamid (MS)

University of Tennessee Health Science Center, Memphis, TN. Electronic address: mhamid2@uthsc.edu.

Sarah C Rutherford (SC)

Weill Cornell Medicine, New York City, NY.

Hyejeong Jang (H)

Karmanos Cancer Institute, Detroit, MI.

Seongho Kim (S)

Karmanos Cancer Institute, Detroit, MI.

Krish Patel (K)

Swedish Cancer Institute, Seattle, WA.

Nancy L Bartlett (NL)

Washington University Medical University at St. Louis, St. Louis, MO.

Mary-Kate Malecek (MK)

Washington University Medical University at St. Louis, St. Louis, MO.

Marcus P Watkins (MP)

Washington University Medical University at St. Louis, St. Louis, MO.

Kami J Maddocks (KJ)

The James Comprehensive Cancer Center, The Ohio State University, Columbus, OH.

David A Bond (DA)

The James Comprehensive Cancer Center, The Ohio State University, Columbus, OH.

Tatyana A Feldman (TA)

John Theurer Cancer Center at Hackensack Meridian Health, Hackensack, NJ.

Gabriela Magarelli (G)

John Theurer Cancer Center at Hackensack Meridian Health, Hackensack, NJ.

Ranjana H Advani (RH)

Stanford Cancer Institute at Stanford University, Stanford, CA.

Michael A Spinner (MA)

Stanford Cancer Institute at Stanford University, Stanford, CA.

Andrew M Evens (AM)

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

Mansi Shah (M)

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

Sairah Ahmed (S)

MD Anderson Cancer Center, Houston, TX.

Deborah M Stephens (DM)

Huntsman Cancer Institute at University of Utah, Salt Lake City, UT.

Pamela Allen (P)

Winship Cancer Institute at Emory University, Atlanta, GA.

Michael T Tees (MT)

Colorado Blood Cancer Institute, Denver, CO.

Reem Karmali (R)

Northwestern University, Chicago, IL.

Bruce D Cheson (BD)

Lombardi Comprehensive Cancer Center, Washington D.C.

Maryam Sarraf Yazdy (MS)

Lombardi Comprehensive Cancer Center, Washington D.C.

Christopher Strouse (C)

University of Iowa, Iowa City, IA.

Neil A Bailey (NA)

Swedish Cancer Institute, Seattle, WA.

John M Pagel (JM)

Swedish Cancer Institute, Seattle, WA.

Radhakrishnan Ramchandren (R)

University of Tennessee Medical Center, Knoxville TN.

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Classifications MeSH