Evidence map›Paper›PMID 33956047›Full record

Observational studyJAMA oncology2021

Outcomes Associated With Thiotepa-Based Conditioning in Patients With Primary Central Nervous System Lymphoma After Autologous Hematopoietic Cell Transplant.

Michael Scordo, Trent P Wang, Kwang W Ahn, Yue Chen, Sairah Ahmed, Farrukh T Awan, Amer Beitinjaneh, Andy Chen, Victor A Chow, Bhagirathbhai Dholaria and 29 more

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in JAMA oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
6.2field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 75 citations in OpenAlex.

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  18. Survival outcomes and treatment experience of 124 patients with primary central nervous system lymphoma.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2024
    Article
  19. Article
  20. Primary central nervous system lymphoma.Journal of neurology · 2024
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

39 authors at 20 institutions in 5 countries.

Michael ScordoAdult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Trent P WangDivision of Transplantation and Cellular Therapy, University of Miami Miller School of Medicine, Miami, Florida.
Kwang W AhnCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee.
Yue ChenCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee.
Sairah AhmedDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Farrukh T AwanDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.
Amer BeitinjanehDivision of Transplantation and Cellular Therapy, University of Miami Miller School of Medicine, Miami, Florida.
Andy ChenDepartment of Medicine, Oregon Health and Science University, Portland.
Victor A ChowFred Hutchinson Cancer Research Center, Seattle, Washington.
Bhagirathbhai DholariaDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Narendranath EpperlaThe James Cancer Hospital and Solove Research Institute, Division of Hematology, Department of Medicine, The Ohio State University, Columbus.
Umar FarooqDivision of Hematology, Oncology and Blood & Marrow Transplantation, University of Iowa Hospitals and Clinics, Iowa City.
Nilanjan GhoshLevine Cancer Institute, Department of Hematologic Oncology and Blood Disorders, Atrium Health, Charlotte, North Carolina.
Natalie GroverDepartment of Medicine, University of North Carolina Hospitals, Chapel Hill.
Nada HamadSt Vincent's Hospital, Darlinghurst, New South Wales, Australia.
Gerhard C HildebrandtMarkey Cancer Center, University of Kentucky, Lexington.
Leona HolmbergFred Hutchinson Cancer Research Center, Seattle, Washington.
Sanghee HongBlood and Marrow Transplant Program, Taussig Cancer Center, Cleveland Clinic, Cleveland, Ohio.
David J InwardsDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Antonio Jimenez-JimenezDivision of Transplantation and Cellular Therapy, University of Miami Miller School of Medicine, Miami, Florida.
Reem KarmaliDepartment of Medicine, Northwestern University, Chicago, Illinois.
Vaishalee P KenkreDepartment of Medicine, University of Wisconsin-Madison, Madison.
Farhad KhimaniH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Evgeny KlyuchnikovDepartment for Stem Cell Transplantation, University Cancer Center, Hamburg, Germany.
Maxwell M KremMarkey Cancer Center, University of Kentucky, Lexington.
Pashna N MunshiDepartment of Medicine, Georgetown University Hospital, Washington, DC.
Yago NietoDepartment of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston.
Tim PrestidgeBlood and Cancer Centre, Starship Children's Hospital, Auckland, New Zealand.
Praveen Ramakrishnan GeethakumariLymphoma, BMT and Cellular Therapy Program, University of Texas Southwestern Medical Center, Dallas.
Andrew R RezvaniDivision of Blood & Marrow Transplantation, Stanford University, Stanford, California.
Peter A RiedellDepartment of Medicine, The University of Chicago Medicine, Chicago, Illinois.
Sachiko SeoDepartment of Hematology and Oncology, Dokkyo Medical University, Tochigi, Japan.
Nirav N ShahDepartment of Medicine, Medical College of Wisconsin, Milwaukee.
Melhem SolhThe Blood and Marrow Transplant Group of Georgia, Northside Hospital, Atlanta.
Jean A YaredBlood & Marrow Transplantation Program, Greenebaum Comprehensive Cancer Center, Division of Hematology/Oncology, Department of Medicine, University of Maryland, Baltimore.
Mohamed A Kharfan-DabajaDivision of Hematology-Oncology, Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, Florida.
Alex HerreraDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, California.
Mehdi HamadaniCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee.
Craig S SauterAdult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Medical College of Wisconsin · USUniversity of Miami · USFred Hutch Cancer Center · USMarkey Cancer Center · USThe University of Texas MD Anderson Cancer Center · USThe University of Texas Southwestern Medical Center · USCity Of Hope National Medical Center · USCleveland Clinic · USCornell University · USDokkyo Medical University · JPGeorgetown University · USLevine Cancer Institute · USMayo Clinic · USMayo Clinic in Florida · USMemorial Sloan Kettering Cancer Center · USMoffitt Cancer Center · USNorthside Hospital · USNorthwestern University · USOregon Health & Science University · USStanford University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

importancePrimary central nervous system lymphoma (PCNSL) requires induction and consolidation to achieve potential cure. High-dose therapy and autologous hematopoietic cell transplant (AHCT) is an accepted and effective consolidation strategy for PCNSL, but no consensus exists on the optimal conditioning regimens.

objectiveTo assess the outcomes in patients with PCNSL undergoing AHCT with the 3 most commonly used conditioning regimens: thiotepa/busulfan/cyclophosphamide (TBC), thiotepa/carmustine (TT-BCNU), and carmustine/etoposide/cytarabine/melphalan (BEAM). DESIGN, SETTING, AND

participantsThis observational cohort study used registry data from the Center for International Blood and Marrow Transplant Research registry. The Center is a working group of more than 380 transplantation centers worldwide that contributed detailed data on HCT to a statistical center at the Medical College of Wisconsin, Milwaukee. The participant data were from 603 adult patients with PCNSL who underwent AHCT as initial, or subsequent, consolidation between January 2010 and December 2018. Patients were excluded if they had a non-Hodgkin lymphoma subtype other than diffuse large B-cell lymphoma, systemic non-Hodgkin lymphoma, or HIV; received an uncommon conditioning regimen; or were not in partial remission or complete remission prior to AHCT. Statistical analysis was performed from July 5, 2020, to March 1, 2021.

interventionsPatients received 1 of 3 conditioning regimens: TBC (n = 263), TT-BCNU (n = 275), and BEAM (n = 65). MAIN OUTCOMES AND MEASURES: The primary outcome was progression-free survival. Secondary outcomes included hematopoietic recovery, incidence of relapse, nonrelapse mortality, and overall survival.

resultsOf 603 patients, the mean age was 57 (range, 19-77) years and 318 (53%) were male. The 3-year adjusted progression-free survival rates were higher in the TBC cohort (75%) and TT-BCNU cohort (76%) compared with the BEAM cohort (58%) (P = .03) owing to a higher relapse risk in the BEAM cohort (hazard ratio [HR], 4.34; 95% CI, 2.45-7.70; P < .001). In a multivariable regression analysis, compared with the TBC cohort, patients who received TT-BCNU had a higher relapse risk (HR, 1.79; 95% CI, 1.07-2.98; P = .03), lower risk of nonrelapse mortality (NRM) (HR, 0.50; 95% CI, 0.29-0.87; P = .01), and similar risk of all-cause mortality more than 6 months after HCT (HR, 1.54; 95% CI, 0.93-2.55; P = .10). Age of 60 years or older, Karnofsky performance status less than 90, and an HCT-comorbidity index greater than or equal to 3 were associated with lower rates of survival across all 3 cohorts. Subgroup analyses demonstrated that patients aged 60 years and older had considerably higher NRM with TBC. CONCLUSIONS AND RELEVANCE: In this cohort study, thiotepa-based conditioning regimen was associated with higher rates of survival compared with BEAM, despite higher rates of early toxic effects and NRM; these findings may assist clinicians in choosing between TBC or TT-BCNU based on patient and disease characteristics.

Indexed as

Hematopoietic Stem Cell TransplantationLymphoma, Non-HodgkinAgedAntineoplastic Combined Chemotherapy ProtocolsCentral Nervous SystemCohort StudiesCyclophosphamideHumansMaleMiddle AgedNeoplasm Recurrence, LocalThiotepaCyclophosphamideThiotepa

Identifiers

PMID33956047
PMCPMC8283558
OpenAlexW3158097874

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.