Page last updated: 2024-11-05

thiotepa and Lymphoma, B-Cell

thiotepa has been researched along with Lymphoma, B-Cell in 6 studies

Thiotepa: A very toxic alkylating antineoplastic agent also used as an insect sterilant. It causes skin, gastrointestinal, CNS, and bone marrow damage. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), thiotepa may reasonably be anticipated to be a carcinogen (Merck Index, 11th ed).

Lymphoma, B-Cell: A group of heterogeneous lymphoid tumors generally expressing one or more B-cell antigens or representing malignant transformations of B-lymphocytes.

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's3 (50.00)29.6817
2010's1 (16.67)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Takahashi, M1
Sumitani, R1
Hori, T1
Murai, J1
Kawata, S1
Oura, M1
Sogabe, K1
Harada, T1
Fujii, S1
Miki, H1
Kagawa, K1
Abe, M1
Nakamura, S1
Ferreri, AJ1
Cwynarski, K1
Pulczynski, E1
Ponzoni, M1
Deckert, M1
Politi, LS1
Torri, V1
Fox, CP1
Rosée, PL1
Schorb, E1
Ambrosetti, A1
Roth, A1
Hemmaway, C1
Ferrari, A1
Linton, KM1
Rudà, R1
Binder, M1
Pukrop, T1
Balzarotti, M1
Fabbri, A1
Johnson, P1
Gørløv, JS1
Hess, G1
Panse, J1
Pisani, F1
Tucci, A1
Stilgenbauer, S1
Hertenstein, B1
Keller, U1
Krause, SW1
Levis, A1
Schmoll, HJ1
Cavalli, F1
Finke, J1
Reni, M1
Zucca, E1
Illerhaus, G1
Soussain, C2
Hoang-Xuan, K2
Levy, V2
Stern, BV1
Baehring, JM1
Kleopa, KA1
Hochberg, FH1
Sandor, V1
Stark-Vancs, V1
Pearson, D1
Nussenblat, R1
Whitcup, SM1
Brouwers, P1
Patronas, N1
Heiss, J1
Jaffe, E1
deSmet, M1
Kohler, D1
Simon, R1
Wittes, R1
Suzan, F1
Cassoux, N1
Azar, N1
Belanger, C1
Achour, E1
Ribrag, V1
Gerber, S1
Delattre, JY1
Leblond, V1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Randomized Phase II Trial On Primary Chemotherapy With High-Dose Methotrexate And High-Dose Cytarabine With Or Without Thiotepa, And With Or Without Rituximab, Followed By Brain Irradiation Vs. High-Dose Chemotherapy Supported By Autologous Stem Cells Tra[NCT01011920]Phase 2126 participants (Actual)Interventional2009-11-30Completed
A Phase 2a Study of the Addition of Temozolomide to a Standard Conditioning Regimen for Autologous Stem Cell Transplantation in Relapsed and Refractory Central Nervous System (CNS) Lymphoma[NCT01235793]Phase 211 participants (Actual)Interventional2010-10-14Terminated (stopped due to The clinical trial was terminated due to poor enrollment)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Safest Dose of Temozolomide for the DRBEAT Regimen

Safety will be assessed using a dose escalation design for temozolomide's use to determine the target dose and also to evaluate any and all acute treatment related toxicities. During the course of patient follow up and therapy, toxicities will be evaluated, particularly as the investigators will be determining the target dose of temozolomide. One of the major criteria for dose limiting toxicity for the study will be any Grade 3 or 4 nonhematologic toxicity from a list of commonly expected toxicities associated with autologous transplantation and temozolomide. (NCT01235793)
Timeframe: One Year

Interventiondose in mg/m^2 (Number)
DRBEAT Regimen773.25

One-year Progression-free Survival and Overall Survival

"Efficacy of the DRBEAT Regimen will be assessed by analysis of~one-year progression-free survival (PFS), defined as the time interval from maximal response from therapy to tumor regrowth, progression*, or death, (*Progression is defined as meeting the response criteria listed in Table 4: Response Criteria for Primary Central Nervous System Lymphoma according to Abrey LE, Batchelor TT, Ferreri AJM et al.)~and~Overall survival, defined as the time interval between the date of transplant and the date of death from any cause." (NCT01235793)
Timeframe: (1) One Year (2) Until date of death from any cause, assessed up to 2 years

InterventionDays (Median)
Progression Free SurvivalOverall Survival
DRBEAT Regimen132564

Trials

3 trials available for thiotepa and Lymphoma, B-Cell

ArticleYear
Chemoimmunotherapy with methotrexate, cytarabine, thiotepa, and rituximab (MATRix regimen) in patients with primary CNS lymphoma: results of the first randomisation of the International Extranodal Lymphoma Study Group-32 (IELSG32) phase 2 trial.
    The Lancet. Haematology, 2016, Volume: 3, Issue:5

    Topics: Acute Kidney Injury; Anemia; Antineoplastic Combined Chemotherapy Protocols; Central Nervous System

2016
Phase II trial of chemotherapy alone for primary CNS and intraocular lymphoma.
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 1998, Volume: 16, Issue:9

    Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Central Nervous System Neoplasms; Cytar

1998
Results of intensive chemotherapy followed by hematopoietic stem-cell rescue in 22 patients with refractory or recurrent primary CNS lymphoma or intraocular lymphoma.
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2001, Feb-01, Volume: 19, Issue:3

    Topics: Adult; Antineoplastic Combined Chemotherapy Protocols; Busulfan; Central Nervous System Neoplasms; C

2001

Other Studies

3 other studies available for thiotepa and Lymphoma, B-Cell

ArticleYear
Intravenous busulfan-based conditioning with autologous stem cell transplantation for refractory B-cell lymphoma with central nervous system involvement.
    The journal of medical investigation : JMI, 2021, Volume: 68, Issue:1.2

    Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Busulfan; Central Nervous System; Combi

2021
[Results of intensive chemotherapy followed by hematopoietic stem-cell rescue in 22 patients with refractory or recurrent primary CNS lymphoma or intraocular lymphoma].
    Bulletin du cancer, 2004, Volume: 91, Issue:2

    Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Busulfan; Central Nervous System Neopla

2004
Multifocal motor neuropathy with conduction block associated with metastatic lymphoma of the nervous system.
    Journal of neuro-oncology, 2006, Volume: 78, Issue:1

    Topics: Antineoplastic Combined Chemotherapy Protocols; Cyclophosphamide; Demyelinating Diseases; Female; He

2006