ifosfamide has been researched along with Diffuse Lymphocytic Lymphoma, Poorly-Differentiated in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (28.57) | 29.6817 |
2010's | 3 (42.86) | 24.3611 |
2020's | 2 (28.57) | 2.80 |
Authors | Studies |
---|---|
Pavlovsky, M | 1 |
Cubero, D | 1 |
Agreda-Vásquez, GP | 1 |
Enrico, A | 1 |
Mela-Osorio, MJ | 1 |
San Sebastián, JA | 1 |
Fogliatto, L | 1 |
Ovilla, R | 1 |
Avendano, O | 1 |
Machnicki, G | 1 |
Barreyro, P | 1 |
Trufelli, D | 1 |
Villanova, P | 1 |
Alderuccio, JP | 1 |
Saul, EE | 1 |
Iyer, SG | 1 |
Reis, IM | 1 |
Alencar, AJ | 1 |
Rosenblatt, JD | 2 |
Lossos, IS | 2 |
Hosein, PJ | 1 |
Morgensztern, D | 1 |
Coleman, F | 1 |
Escalón, MP | 1 |
Byrne, GE | 1 |
Walker, GR | 1 |
Stewart, DA | 1 |
Duan, Q | 1 |
Carlson, L | 1 |
Russell, JA | 1 |
Bahlis, NJ | 1 |
Duggan, P | 1 |
Hasegawa, W | 1 |
Voralia, M | 1 |
Cartier, JC | 1 |
Truche, AS | 1 |
Tonini, J | 1 |
Zaoui, P | 1 |
Carron, PL | 1 |
Corazzelli, G | 1 |
Russo, F | 1 |
Capobianco, G | 1 |
Marcacci, G | 1 |
Della Cioppa, P | 1 |
Pinto, A | 1 |
Hertzberg, MS | 1 |
Crombie, C | 1 |
Benson, W | 1 |
Taper, J | 1 |
Gottlieb, D | 1 |
Bradstock, KF | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Phase II Study of Rituximab in Combination With Methotrexate, Doxorubicin, Cyclophosphamide, Leucovorin, Vincristine, Ifosfamide, Etoposide, Cytarabine and Mesna (R-MACLO/VAM) in Patients With Previously Untreated Mantle Cell Lymphoma[NCT00878254] | Phase 2 | 25 participants (Actual) | Interventional | 2009-03-25 | Active, not recruiting | ||
Phase II Study of Rituximab in Combination With Methotrexate, Doxorubicin, Cyclophosphamide, Leucovorin, Vincristine, Ifosfamide, Etoposide, Cytarabine and Mesna (MACLO/IVAM) in Patients With Previously Untreated Mantle Cell Lymphoma[NCT00450801] | Phase 2 | 22 participants (Actual) | Interventional | 2004-04-30 | Completed | ||
Long-term Follow-up and/or Continued Thalidomide (THALOMID®) Maintenance Therapy for Patients Enrolled on Clinical Trial 20030165[NCT02507336] | Phase 2 | 2 participants (Actual) | Interventional | 2015-11-24 | Completed | ||
High Dose Chemotherapy and Autologous or Allogeneic Blood Stem Cell Transplantation for Mantle Cell and Relapsed Low Grade Non-hodgkin's Lymphoma[NCT00144092] | Phase 2 | 60 participants (Anticipated) | Interventional | 2001-05-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Number of patients experiencing adverse events during the course of protocol therapy. (NCT00450801)
Timeframe: Up to 5 years
Intervention | participants (Number) |
---|---|
R-MACLO Cycles | 22 |
R-IVAM Cycles | 22 |
Thalidomide Therapy | 19 |
Percentage of participants achieving complete response (CR) to protocol therapy according to International Working Group Response Criteria for Non-Hodgkin's Lymphoma (NHL) using the CT imaging method. Patients were classified by best tumor response; CR was defined as normalization of the lactate dehydrogenase (LDH), complete disappearance of disease-related symptoms and lymph nodes, and clearance of lymphoma from involved organs; complete response unconfirmed (CRu) as a residual lymph node greater than 1.5 cm in greatest transverse diameter that had regressed by more than 75% or an indeterminate bone marrow examination; partial response (PR) as greater than 50% reduction in the involved lymph nodes, or disappearance of the involved lymph nodes but persistent bone marrow involvement; relapse/progression as new or increased lymph nodes, organomegaly, or reappearance of bone marrow involvement. (NCT00450801)
Timeframe: Up to 5 years
Intervention | percentage of participants (Number) |
---|---|
R-MACLO-IVAM-T | 100 |
Percentage of participants who are alive up to five years after receipt of protocol therapy. (NCT00450801)
Timeframe: Up to 5 years
Intervention | percentage of participants (Number) | ||||
---|---|---|---|---|---|
1-year rate overall survival Rate | 2-year overall survival Rate | 3-year overall survival rate | 4-year overall survival rate | 5-year overall survival rate | |
R-MACLO-IVAM-T | 96 | 96 | 96 | 87 | 87 |
Percentage of participants achieving progression-free survival at 1, 3 and 5 years after the start of protocol therapy, based upon the International Working Group Response Criteria for Non-Hodgkin's Lymphoma (NHL). Progression is defined as a ≥ 50% increase from nadir in the product of the two largest perpendicular diameters (PPD-size) of any previously identified abnormal node, or appearance of any new lesion. (NCT00450801)
Timeframe: Up to 5 years
Intervention | percentage of participants (Number) | ||
---|---|---|---|
1 year progression-free survival | 3 year progression-free survival | 5-year progression-free survival | |
R-MACLO-IVAM-T | 91 | 78 | 69 |
3 trials available for ifosfamide and Diffuse Lymphocytic Lymphoma, Poorly-Differentiated
4 other studies available for ifosfamide and Diffuse Lymphocytic Lymphoma, Poorly-Differentiated
Article | Year |
---|---|
Clinical Outcomes of Patients With B-Cell Non-Hodgkin Lymphoma in Real-World Settings: Findings From the Hemato-Oncology Latin America Observational Registry Study.
Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Carboplatin; Cyclophosphamide; Etoposid | 2022 |
Hemodialysis as a treatment of ifosfamide intoxication.
Topics: Humans; Ifosfamide; Lymphoma, Mantle-Cell; Male; Medication Errors; Middle Aged; Poisoning; Renal Di | 2013 |
Gemcitabine, ifosfamide, oxaliplatin and rituximab (R-GIFOX), a new effective cytoreductive/mobilizing salvage regimen for relapsed and refractory aggressive non-Hodgkin's lymphoma: results of a pilot study.
Topics: Adolescent; Adult; Aged; Antibodies, Monoclonal; Antibodies, Monoclonal, Murine-Derived; Antineoplas | 2006 |
Outpatient fractionated ifosfamide, carboplatin and etoposide as salvage therapy in relapsed and refractory non-Hodgkin's and Hodgkin's lymphoma.
Topics: Adolescent; Adult; Aged; Ambulatory Care; Antineoplastic Combined Chemotherapy Protocols; Carboplati | 2006 |