thalidomide has been researched along with Leukemia, Myelomonocytic, Chronic in 7 studies
Thalidomide: A piperidinyl isoindole originally introduced as a non-barbiturate hypnotic, but withdrawn from the market due to teratogenic effects. It has been reintroduced and used for a number of immunological and inflammatory disorders. Thalidomide displays immunosuppressive and anti-angiogenic activity. It inhibits release of TUMOR NECROSIS FACTOR-ALPHA from monocytes, and modulates other cytokine action.
thalidomide : A racemate comprising equimolar amounts of R- and S-thalidomide.
2-(2,6-dioxopiperidin-3-yl)-1H-isoindole-1,3(2H)-dione : A dicarboximide that is isoindole-1,3(2H)-dione in which the hydrogen attached to the nitrogen is substituted by a 2,6-dioxopiperidin-3-yl group.
Leukemia, Myelomonocytic, Chronic: A myelodysplastic-myeloproliferative disease characterized by monocytosis, increased monocytes in the bone marrow, variable degrees of dysplasia, but an absence of immature granulocytes in the blood.
Excerpt | Relevance | Reference |
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"We examined the efficacy of thalidomide in 34 patients with myelodysplastic syndromes (MDS): five RAEB-T, four RAEB, three CMML, six RARS, and 16 RA." | 7.71 | Thalidomide for the treatment of patients with myelodysplastic syndromes. ( Aivado, M; Gattermann, N; Germing, U; Haas, R; Misgeld, E; Strupp, C, 2002) |
"The myelodysplastic syndromes are a heterogeneous group of clonal diseases of haemopoiesis, which are a challenge for both biologists and clinicians." | 6.41 | Thalidomide in myelodysplastic syndromes. ( Pozzato, G; Zorat, F, 2002) |
"We examined the efficacy of thalidomide in 34 patients with myelodysplastic syndromes (MDS): five RAEB-T, four RAEB, three CMML, six RARS, and 16 RA." | 3.71 | Thalidomide for the treatment of patients with myelodysplastic syndromes. ( Aivado, M; Gattermann, N; Germing, U; Haas, R; Misgeld, E; Strupp, C, 2002) |
"We report the cases of 3 patients with hematological malignancies and complex karyotypes involving der(5; 17) (p10;q10), which results in the loss of 5q and 17p." | 2.50 | der(5;17)(p10;q10) is a recurrent but rare whole-arm translocation in patients with hematological neoplasms: a report of three cases. ( Aoyama, Y; Furukawa, Y; Harada, N; Kumura, T; Manabe, M; Mugitani, A; Ohta, T; Okita, J; Tarakuwa, T, 2014) |
"The myelodysplastic syndromes are a heterogeneous group of clonal diseases of haemopoiesis, which are a challenge for both biologists and clinicians." | 2.41 | Thalidomide in myelodysplastic syndromes. ( Pozzato, G; Zorat, F, 2002) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 4 (57.14) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
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Sekeres, MA | 1 |
Othus, M | 1 |
List, AF | 1 |
Odenike, O | 1 |
Stone, RM | 1 |
Gore, SD | 1 |
Litzow, MR | 1 |
Buckstein, R | 2 |
Fang, M | 1 |
Roulston, D | 1 |
Bloomfield, CD | 1 |
Moseley, A | 1 |
Nazha, A | 1 |
Zhang, Y | 1 |
Velasco, MR | 1 |
Gaur, R | 1 |
Atallah, E | 1 |
Attar, EC | 1 |
Cook, EK | 1 |
Cull, AH | 1 |
Rauh, MJ | 1 |
Appelbaum, FR | 1 |
Erba, HP | 1 |
Manabe, M | 1 |
Okita, J | 1 |
Tarakuwa, T | 1 |
Harada, N | 1 |
Aoyama, Y | 1 |
Kumura, T | 1 |
Ohta, T | 1 |
Furukawa, Y | 1 |
Mugitani, A | 1 |
Kerbel, R | 1 |
Cheung, M | 1 |
Shaked, Y | 1 |
Chodirker, L | 1 |
Lee, CR | 1 |
Lenis, M | 1 |
Davidson, C | 1 |
Cussen, MA | 1 |
Reis, M | 1 |
Chesney, A | 1 |
Zhang, L | 1 |
Mamedov, A | 1 |
Wells, RA | 1 |
Kenealy, M | 1 |
Patton, N | 1 |
Filshie, R | 1 |
Nicol, A | 1 |
Ho, SJ | 1 |
Hertzberg, M | 1 |
Mills, T | 1 |
Prosser, I | 1 |
Link, E | 1 |
Cowan, L | 1 |
Zannino, D | 1 |
Seymour, JF | 1 |
Steensma, DP | 1 |
Tefferi, A | 1 |
Strupp, C | 1 |
Germing, U | 1 |
Aivado, M | 1 |
Misgeld, E | 1 |
Haas, R | 1 |
Gattermann, N | 1 |
Zorat, F | 1 |
Pozzato, G | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
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"Revlimid®, and Metronomic Melphalan in the Management of Higher Risk Myelodysplastic Syndromes (MDS) and CMML: A Phase 2 Study"[NCT00744536] | Phase 2 | 20 participants (Actual) | Interventional | 2008-01-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
3 reviews available for thalidomide and Leukemia, Myelomonocytic, Chronic
Article | Year |
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der(5;17)(p10;q10) is a recurrent but rare whole-arm translocation in patients with hematological neoplasms: a report of three cases.
Topics: Aged; Aged, 80 and over; Anemia, Refractory, with Excess of Blasts; Aneuploidy; Antineoplastic Combi | 2014 |
Risk-based management of myelodysplastic syndrome.
Topics: Anemia, Sideroblastic; Antilymphocyte Serum; Azacitidine; Benzoates; Decitabine; Deferasirox; DNA Mo | 2007 |
Thalidomide in myelodysplastic syndromes.
Topics: Anemia, Refractory; Anemia, Refractory, with Excess of Blasts; Antineoplastic Agents; Chromosome Abe | 2002 |
3 trials available for thalidomide and Leukemia, Myelomonocytic, Chronic
Article | Year |
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Randomized Phase II Study of Azacitidine Alone or in Combination With Lenalidomide or With Vorinostat in Higher-Risk Myelodysplastic Syndromes and Chronic Myelomonocytic Leukemia: North American Intergroup Study SWOG S1117.
Topics: Adult; Aged; Aged, 80 and over; Antimetabolites, Antineoplastic; Antineoplastic Combined Chemotherap | 2017 |
Lenalidomide and metronomic melphalan for CMML and higher risk MDS: a phase 2 clinical study with biomarkers of angiogenesis.
Topics: Aged; Aged, 80 and over; Biomarkers; Endothelial Cells; Humans; Lenalidomide; Leukemia, Myelomonocyt | 2014 |
Results of a phase II study of thalidomide and azacitidine in patients with clinically advanced myelodysplastic syndromes (MDS), chronic myelomonocytic leukemia (CMML) and low blast count acute myeloid leukemia (AML).
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Azacitidine; Bone Ma | 2017 |
1 other study available for thalidomide and Leukemia, Myelomonocytic, Chronic
Article | Year |
---|---|
Thalidomide for the treatment of patients with myelodysplastic syndromes.
Topics: Aged; Aged, 80 and over; Anemia, Refractory; Anemia, Refractory, with Excess of Blasts; Blood Transf | 2002 |