1-anilino-8-naphthalenesulfonate has been researched along with Precursor Cell Lymphoblastic Leukemia-Lymphoma in 7 studies
1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd
8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.
Precursor Cell Lymphoblastic Leukemia-Lymphoma: A neoplasm characterized by abnormalities of the lymphoid cell precursors leading to excessive lymphoblasts in the marrow and other organs. It is the most common cancer in children and accounts for the vast majority of all childhood leukemias.
Excerpt | Relevance | Reference |
---|---|---|
"Ponatinib (AP24534) is a potent oral tyrosine kinase inhibitor that blocks native and mutated BCR-ABL, including the gatekeeper mutant T315I, which is uniformly resistant to tyrosine kinase inhibitors." | 2.77 | Ponatinib in refractory Philadelphia chromosome-positive leukemias. ( Bixby, D; Clackson, T; Cortes, JE; Deininger, MW; Druker, BJ; Flinn, I; Haluska, FG; Hu, S; Kantarjian, H; Mauro, MJ; Narasimhan, NI; O'Hare, T; Rivera, VM; Shah, NP; Talpaz, M; Turner, CD, 2012) |
"In this study, no clinically significant acute pancreatitis occurred." | 1.72 | The Effect of Chemotherapy Induction Therapy on the Pancreas in Patients with Acute Lymphoblastic Leukemia. ( Mekonnen, AT; Wondmeneh, TG, 2022) |
"Remission induction therapy for acute lymphoblastic leukemia (ALL) includes medications that may cause hepatotoxicity, including asparaginase." | 1.46 | Genome-Wide Study Links PNPLA3 Variant With Elevated Hepatic Transaminase After Acute Lymphoblastic Leukemia Therapy. ( Carroll, WL; Cheng, C; Devidas, M; Evans, WE; Fernandez, CA; Hunger, SP; Janke, LJ; Jeha, S; Karol, SE; Kornegay, N; Larsen, EC; Liu, C; Liu, Y; Loh, ML; Mullighan, CG; Panetta, JC; Pui, CH; Raetz, EA; Ramsey, LB; Relling, MV; Smith, C; Winick, N; Yang, JJ; Yang, W; Zhang, J, 2017) |
"The hypercholesterolemia was caused by cholestasis due to chronic GVHD and ischemic cholangiopathy." | 1.33 | Severe hypercholesterolemia associated with decreased hepatic triglyceride lipase activity and pseudohyponatremia in patients after allogeneic stem cell transplantation. ( Hirabayashi, N; Inamoto, Y; Kodera, Y; Miyamura, K; Sanda, T; Shirai, K; Teramoto, T; Tsukamoto, H; Yamamori, I, 2005) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 2 (28.57) | 29.6817 |
2010's | 3 (42.86) | 24.3611 |
2020's | 1 (14.29) | 2.80 |
Authors | Studies |
---|---|
Wondmeneh, TG | 1 |
Mekonnen, AT | 1 |
Guruprasad, CS | 1 |
Reghu, KS | 1 |
Nair, M | 1 |
Kumary, PK | 1 |
Liu, Y | 1 |
Fernandez, CA | 1 |
Smith, C | 1 |
Yang, W | 1 |
Cheng, C | 1 |
Panetta, JC | 1 |
Kornegay, N | 1 |
Liu, C | 1 |
Ramsey, LB | 1 |
Karol, SE | 1 |
Janke, LJ | 1 |
Larsen, EC | 1 |
Winick, N | 1 |
Carroll, WL | 1 |
Loh, ML | 1 |
Raetz, EA | 1 |
Hunger, SP | 1 |
Devidas, M | 1 |
Yang, JJ | 1 |
Mullighan, CG | 1 |
Zhang, J | 1 |
Evans, WE | 1 |
Jeha, S | 1 |
Pui, CH | 1 |
Relling, MV | 1 |
Cortes, JE | 1 |
Kantarjian, H | 1 |
Shah, NP | 1 |
Bixby, D | 1 |
Mauro, MJ | 1 |
Flinn, I | 1 |
O'Hare, T | 1 |
Hu, S | 1 |
Narasimhan, NI | 1 |
Rivera, VM | 1 |
Clackson, T | 1 |
Turner, CD | 1 |
Haluska, FG | 1 |
Druker, BJ | 1 |
Deininger, MW | 1 |
Talpaz, M | 1 |
Inamoto, Y | 1 |
Teramoto, T | 1 |
Shirai, K | 1 |
Tsukamoto, H | 1 |
Sanda, T | 1 |
Miyamura, K | 1 |
Yamamori, I | 1 |
Hirabayashi, N | 1 |
Kodera, Y | 1 |
Malbora, B | 1 |
Avci, Z | 1 |
Alioglu, B | 1 |
Tutar, NU | 1 |
Ozbek, N | 1 |
Shimizu, T | 1 |
Yamashiro, Y | 1 |
Igarashi, J | 1 |
Fujita, H | 1 |
Ishimoto, K | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Total XV - Total Therapy Study XV for Newly Diagnosed Patients With Acute Lymphoblastic Leukemia[NCT00137111] | Phase 3 | 501 participants (Actual) | Interventional | 2000-07-08 | Completed | ||
A Phase 1 Dose Escalation Trial to Determine the Safety, Tolerability and Maximum Tolerated Dose of Oral AP24534 in Patients With Refractory or Advanced Chronic Myelogenous Leukemia and Other Hematologic Malignancies[NCT00660920] | Phase 1 | 81 participants (Actual) | Interventional | 2008-06-30 | Completed | ||
Phase 2 Trial of Ponatinib in Patients With Metastatic and/or Unresectable Gastrointestinal Stromal Tumor (GIST) Following Failure or Intolerance of Prior Therapy With Imatinib[NCT03171389] | Phase 2 | 81 participants (Anticipated) | Interventional | 2017-03-22 | Recruiting | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
"White blood cell (leukocytes) counts in peripheral blood by Complete Blood Count~Measurement: Percentage change of leukemia cells from baseline" (NCT00137111)
Timeframe: Immediately before the methotrexate infusion and three days after subsequent infusion
Intervention | Percent change (Mean) |
---|---|
4 hr | -44 |
24 hr | -50 |
CCR was measured from end of week 56 therapy to the date of first treatment failure of any kind (relapse, death, lineage switch, or second malignancy) or to the last date of follow-up. Measurement was determined by Kaplan-Meyer estimate. (NCT00137111)
Timeframe: Median follow up time (range) 4.5 (1 to 7.8) years
Intervention | Percentage of participants (Number) |
---|---|
Patients With High Risk of CNS Relapse | 92.2 |
Children were randomly assigned to receive initial single-agent treatment with HDMTX (1g/m^2) as either a 24-hour infusion or a 4-hour infusion and the outcome measure was the accumulation of MTXPG in leukemia cells. (NCT00137111)
Timeframe: 42 hours after start of high dose methotrexate infusion (HDMTX)
Intervention | pmol/1,000,000,000 cells (Mean) |
---|---|
4 hr | 1688 |
24 hr | 2521 |
EFS was measured from the start of on-study to the date of first treatment failure of any kind (relapse, death, lineage switch, or second malignancy) or to the last date of follow-up. Failure to enter remission was considered an event at time zero. Measurement was determined by Kaplan-Meyer estimate. (NCT00137111)
Timeframe: Median follow-up time (range) 5.6 (1.3 to 8.9) years
Intervention | Percentage of Participants (Number) |
---|---|
Total Therapy | 87.3 |
Prednisolone sensitivity was measured in primary leukemia cells from bone marrow collected at diagnosis. Expression of CASP1 was determined by HG-U133A microarray. Values given are gene expression values, and the unit is arbitrary units (AU) defined as scaled fluorescence measured on microarray. (NCT00137111)
Timeframe: Pre-treatment
Intervention | arbitrary units (Median) | |
---|---|---|
Prednisolone-sensitive cells | Prednisolone-resistant cells | |
Total Therapy | 341.3 | 447.9 |
Prednisolone sensitivity was measured in primary leukemia cells from bone marrow collected at diagnosis. Expression of NLRP3 was determined by HG-U133A microarray. Values given are gene expression values, and the unit is arbitrary units (AU) defined as scaled fluorescence measured on microarray. (NCT00137111)
Timeframe: Pre-treatment
Intervention | arbitrary units (Median) | |
---|---|---|
Prednisolone-sensitive cells | Prednisolone-resistant cells | |
Total Therapy | 41.2 | 110.7 |
Detection of MRD at end of induction where positive MRD was defined as one or more leukemic cell per 10,000 mononuclear bone-marrow cells (>=0.01%). (NCT00137111)
Timeframe: End of Induction (Day 46 MRD measurement)
Intervention | participants (Number) | |
---|---|---|
Negative <0.01% | Positive >= 0.01% | |
Total Therapy | 390 | 102 |
1 trial available for 1-anilino-8-naphthalenesulfonate and Precursor Cell Lymphoblastic Leukemia-Lymphoma
Article | Year |
---|---|
Ponatinib in refractory Philadelphia chromosome-positive leukemias.
Topics: Adult; Aged; Aged, 80 and over; Amylases; Antineoplastic Agents; Dose-Response Relationship, Drug; D | 2012 |
Ponatinib in refractory Philadelphia chromosome-positive leukemias.
Topics: Adult; Aged; Aged, 80 and over; Amylases; Antineoplastic Agents; Dose-Response Relationship, Drug; D | 2012 |
Ponatinib in refractory Philadelphia chromosome-positive leukemias.
Topics: Adult; Aged; Aged, 80 and over; Amylases; Antineoplastic Agents; Dose-Response Relationship, Drug; D | 2012 |
Ponatinib in refractory Philadelphia chromosome-positive leukemias.
Topics: Adult; Aged; Aged, 80 and over; Amylases; Antineoplastic Agents; Dose-Response Relationship, Drug; D | 2012 |
6 other studies available for 1-anilino-8-naphthalenesulfonate and Precursor Cell Lymphoblastic Leukemia-Lymphoma
Article | Year |
---|---|
The Effect of Chemotherapy Induction Therapy on the Pancreas in Patients with Acute Lymphoblastic Leukemia.
Topics: Acute Disease; Adult; Amylases; Child; Humans; Induction Chemotherapy; Lipase; Pancreas; Pancreatiti | 2022 |
Asymptomatic Hyperamylasemia / Hyperlipasemia due to Pancreatic Infiltration in Acute Lymphoblastic Leukemia.
Topics: Antineoplastic Agents; Bone Marrow Examination; Child; Endoscopic Ultrasound-Guided Fine Needle Aspi | 2016 |
Genome-Wide Study Links PNPLA3 Variant With Elevated Hepatic Transaminase After Acute Lymphoblastic Leukemia Therapy.
Topics: Alanine Transaminase; Antineoplastic Agents; Asparaginase; Chemical and Drug Induced Liver Injury; C | 2017 |
Severe hypercholesterolemia associated with decreased hepatic triglyceride lipase activity and pseudohyponatremia in patients after allogeneic stem cell transplantation.
Topics: ABO Blood-Group System; Adult; Blood Group Incompatibility; Female; Humans; Hypercholesterolemia; Hy | 2005 |
A case with mature B-cell acute lymphoblastic leukemia and pancreatic involvement at the time of diagnosis.
Topics: Acute Disease; Amylases; Antineoplastic Combined Chemotherapy Protocols; Child, Preschool; Diagnosis | 2008 |
Increased serum trypsin and elastase-1 levels in patients undergoing L-asparaginase therapy.
Topics: Acute Disease; Adolescent; Amylases; Antineoplastic Agents; Asparaginase; Child; Child, Preschool; F | 1998 |