Promoter mutation analysis of PMS2 gene in solid tumors and acute leukemias

2019 ◽  
Vol 215 (10) ◽  
pp. 152583
Author(s):  
Ha Yoon Mo ◽  
Eun Ji Choi ◽  
Nam Jin Yoo ◽  
Sug Hyung Lee
2019 ◽  
Vol 141 (4) ◽  
pp. 214-215
Author(s):  
Ha Yoon Mo ◽  
Min Sung Kim ◽  
Nack Gyun Chung ◽  
Nam Jin Yoo ◽  
Sug Hyung Lee

2018 ◽  
Vol 25 (2) ◽  
pp. 825-826 ◽  
Author(s):  
Hyun Ji Son ◽  
Eun Ji Choi ◽  
Nam Jin Yoo ◽  
Sug Hyung Lee

2019 ◽  
Vol 26 (4) ◽  
pp. 2809-2810
Author(s):  
Hyun Ji Son ◽  
Ha Yoon Mo ◽  
Eun Ji Choi ◽  
Nam Jin Yoo ◽  
Sug Hyung Lee

2020 ◽  
Vol 27 (1) ◽  
pp. 169-178
Author(s):  
Koushik Muralidharan ◽  
Anudeep Yekula ◽  
Julia L. Small ◽  
Zachary S. Rosh ◽  
Keiko M. Kang ◽  
...  

1997 ◽  
Vol 32 (8) ◽  
pp. 1175-1180 ◽  
Author(s):  
Takeshi Kusafuka ◽  
Masahiro Fukuzawa ◽  
Takaharu Oue ◽  
Yosuke Komoto ◽  
Akihiro Yoneda ◽  
...  

2015 ◽  
Vol 22 (1) ◽  
pp. 223-224 ◽  
Author(s):  
Hye Rim Oh ◽  
Youn Jin Choi ◽  
Nam Jin Yoo ◽  
Sug Hyung Lee

2016 ◽  
Vol 34 (15_suppl) ◽  
pp. e23246-e23246
Author(s):  
Ling Xu ◽  
Xiujuan Qu ◽  
Rui Ma ◽  
Yuee Teng ◽  
Jingdong Zhang ◽  
...  

2020 ◽  
Vol 38 (15_suppl) ◽  
pp. TPS10560-TPS10560
Author(s):  
Theodore Willis Laetsch ◽  
Kathleen Ludwig ◽  
Donald A. Barkauskas ◽  
Steven G. DuBois ◽  
Joan Ronan ◽  
...  

TPS10560 Background: In children, fusions of the NTRK1/2/3 genes (TRK fusions) occur in soft tissue sarcomas, including infantile fibrosarcoma (IFS), congenital mesoblastic nephroma, high- and low-grade gliomas, secretory breast carcinoma, and papillary thyroid cancer. Rarely, TRK fusions also occur in Ph-like acute lymphoblastic leukemia and acute myeloid leukemia. Larotrectinib is a selective TRK inhibitor FDA-approved for the treatment of TRK fusion solid tumors in patients with no satisfactory alternative treatments or whose cancer has progressed following initial treatment. In children, larotrectinib demonstrated a 94% overall response rate (ORR) with a 12-month progression free survival rate of 75% (1). Methods: Patients <30 years with any newly diagnosed unresectable solid tumor or relapsed/refractory acute leukemia with TRK fusions are eligible. TRK fusions must be locally identified in a CLIA/CAP laboratory and are confirmed centrally using a targeted RNA sequencing panel. Patients with high-grade gliomas are excluded. Patients receive larotrectinib 100 mg/m2/dose BID (max of 100 mg/dose) continuously in 28-day cycles. Patients with solid tumors who achieve CR will discontinue larotrectinib at the completion of at least 12 total cycles of therapy and 6 cycles after achieving CR. Those whose tumors become surgically resectable may undergo on study resection and discontinue therapy if an R0/R1 (IFS) or R0 (other tumors) resection is obtained. All other patients will receive 26 cycles in the absence of unacceptable toxicity or progressive disease. The primary endpoint is the ORR to larotrectinib according to RECIST 1.1 in children with IFS. The study uses a Simon 2-stage minimax design, and the regimen will be considered of sufficient interest if 16 of 21 (76%) patients with IFS demonstrate response. Patients with other solid tumors and leukemias will be analyzed in separate cohorts as secondary objectives. Correlative studies include serial sampling of circulating tumor DNA and neurocognitive assessments. This is the first Children’s Oncology Group study to assign frontline therapy based on the presence of a molecular marker independent of histology, and the first clinical trial to evaluate larotrectinib for the treatment of leukemia. Enrollment began in October 2019 (NCT03834961). 1. Tilburg CMv, DuBois SG, Albert CM, et al: Larotrectinib efficacy and safety in pediatric TRK fusion cancer patients. Journal of Clinical Oncology 37:10010-10010, 2019 Clinical trial information: NCT03834961.


Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 3143-3143 ◽  
Author(s):  
Helen Baldomero ◽  
Mahmoud Aljurf ◽  
Luis Fernando Bouzas ◽  
Alois Gratwohl ◽  
Yoshihisa Kodera ◽  
...  

Abstract Abstract 3143 Hematopoietic cell transplantation (HCT) is the treatment of choice for many patients with malignant and non-malignant disorders. Transplant practices have evolved allowing patients previously not otherwise candidates to receive this procedure. Activity surveys and registries play an essential role in the success of HCT, by tracking activities, identifying areas of need and through clinical research to continue improving patient outcome. Because of the need of matched donors, ethnic characteristics and legal requirements HCT has acquired a global dimension. In the current analysis the Worldwide Blood and Marrow Transplantation network (WBMT) reports the global activities, indications and trends for the years 2006 to 2008. The survey consisted of activities reported to the WBMT from international societies members (EBMT, CIBMTR, APBMT, EMBMT, ABMTRR), national registries (SBTMO) and also directly from transplant centers in regions were no societies are established. Annual transplant center specific activities were from 1327 transplant centers in 71 countries in 2006. The number of participating centers increased to 1382 and 1407 in 2007 and 2008, respectively. Annual number of transplants steadily increased from 46,563 in 2006 to 48,709 and 51,536 in 2007 and 2008. When analyzing the median number of transplants/year performed at each center the corresponding annual activity was 38 (range 3–180), 46 (3–421) and 48 (1–389), suggesting that the increment in transplant activity is not only related to higher number of reporting centers. The highest increase in total HCT over two years was observed in the Asia Pacific region (38.6%) followed by the East Mediterranean region (19.4%), Europe (5.6%) and the U.S. (4.5%). An absolute increase of autologous and allogeneic was observed over the three year period with more autologous (55%) than allogeneic (45%) HCT reported, however the increase was less in autologous (+5.0%) when compared to allogeneic (+17.9%). Among indications for allogeneic HCT, acute leukemias (AML +23%; ALL +27%), myelodysplasia (MDS +26%), chronic lymphocytic leukemia (CLL +24.6%) nonmalignant diseases (NMD +23.6%) and bone marrow failure disorders (BMF +21.2%) significantly increased during the study period. Slower increase was reported for lymphoproliferative disorders (LPD +6%) and a clear decrease for chronic myelogenous leukemia (CML -17%) and solid tumors (−13.3%). Among autologous HCT indications autoimmune diseases (+24.5%), PCD (+9.8%) and LPD (+7.5%) increased during the period. A negative trend was seen in autologous HCT for solid tumors (−2.4%), ALL (−22.0%), AML (−9.0%), CLL (−52.0%) and CML (−57.1%). These data show the trend and activity for autologous and allogeneic HSCT worldwide. There is a clear increase in activity especially in acute and chronic (except CML) leukemias for allogeneic HST and for autoimmune diseases, LPD and PCD in autologous HCT. Monitoring global transplant practices is an important activity for WBMT in order for capacity planning of HCT donor pool worldwide and to promote the field by expanding access to transplantation at regions in need. Disclosures: No relevant conflicts of interest to declare.


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