The goal of the T32 Investigational Cancer Therapeutics Training Program (ICTTP) at Memorial Sloan- Kettering Cancer Center (MSKCC) is to provide highly select physician trainees in hematology and medical oncology with the research training necessary for successful careers in the translation of cancer biology discoveries into novel molecular, immune, or cell-based therapeutics, and those experimental treatments into clinical trials that have the potential to change standards of care. The T32 ICTTP program accomplishes this goal by combining a comprehensive mentored training program, an extensive didactic curriculum in clinical and translational research methodologies, and experiential programs supporting development of the critical career skills (e.g. collaboration, research management, grant writing) necessary for academic success. Each year, we select 4 highly committed postdoctoral trainees from the pool of outstanding physicians at MSKCC who have completed at least 3-4 years of both internal medicine and oncology/hematology clinical training. T32 trainees are then supported for 2 consecutive years so that ? 80% of their time and effort is dedicated to research training. Based on individual research interests and career goals, ICCTP trainees develop either a laboratory- based or a prospective clinical research program with guidance from their mentors, who are established, independently funded investigators. These programs involve extensive collaborative scientific interactions, including additional clinical scientist mentorship for laboratory-based trainees and laboratory scientist mentorship for clinical research trainees. The T32 ICTTP supplements mentored research training with a curriculum of symposia, workshops, in-person didactic programs, and online courses that prepares trainees to conduct successful, independently supported research at the faculty level. We continue to enhance the program by revising and adding new educational programs in clinical research methodology, research ethics, national and international clinical trial requirements and conduct, as well as hands-on writing workshops for grants and protocols. Participating faculty mentors are continually reviewed and selected based on strict criteria for research productivity, independent funding, and quality of mentoring. T32 ICTTP mentors have research programs on cancer genetics, genomics, epigenetics, signal transduction, and metabolism; tumor immunology and immunotherapy; drug and cellular therapeutic development; and tumor evolution, using systems and computational approaches. Projects conducted by T32 ICTTP trainees in the proposed funding period continue similar themes in cancer therapeutics research. All T32 ICTTP graduates from the last funding cycle are continuing in oncology research, and all who are working in academia have secured independent research funding. This success continues the ICTTP?s 40-year track record of training leaders in cancer therapeutic development and translational research.

Public Health Relevance

Accelerating the future development of new cancer treatments requires educating the next generation of leaders in this field in the complex interactions between tumors, their surroundings, and the immune system, and preparing them to efficiently conduct research in today?s regulatory and administrative environment. The T32 Investigational Cancer Therapeutics Training Program (ICTTP) at Memorial Sloan Kettering Cancer Center addresses this need by providing fellows in medical oncology who are committed to careers in translational cancer research with comprehensive mentored research and didactic training for two years. The ICTTP program is designed to optimally train physician scientists to translate discoveries regarding the biology of cancer into new, approved molecular/cytotoxic, immunotherapeutic, and cell-based treatments through state-of-the-art experimental trials. !

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Institutional National Research Service Award (T32)
Project #
2T32CA009207-41
Application #
9853229
Study Section
Subcommittee I - Transistion to Independence (NCI)
Program Officer
Lim, Susan E
Project Start
1977-09-30
Project End
2024-08-31
Budget Start
2019-09-11
Budget End
2020-08-31
Support Year
41
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Sloan-Kettering Institute for Cancer Research
Department
Type
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10065
Offin, Michael; Rizvi, Hira; Tenet, Megan et al. (2018) Tumor Mutation Burden and Efficacy of EGFR-Tyrosine Kinase Inhibitors in Patients with EGFR-Mutant Lung Cancers. Clin Cancer Res :
Sharma, Sai Kiran; Chow, Andrew; Monette, Sebastien et al. (2018) Fc-Mediated Anomalous Biodistribution of Therapeutic Antibodies in Immunodeficient Mouse Models. Cancer Res 78:1820-1832
Avanzi, Mauro P; Yeku, Oladapo; Li, Xinghuo et al. (2018) Engineered Tumor-Targeted T Cells Mediate Enhanced Anti-Tumor Efficacy Both Directly and through Activation of the Endogenous Immune System. Cell Rep 23:2130-2141
Hyman, David M; Piha-Paul, Sarina A; Won, Helen et al. (2018) HER kinase inhibition in patients with HER2- and HER3-mutant cancers. Nature 554:189-194
Rekhtman, Natasha; Pietanza, Catherine M; Sabari, Joshua et al. (2018) Pulmonary large cell neuroendocrine carcinoma with adenocarcinoma-like features: napsin A expression and genomic alterations. Mod Pathol 31:111-121
Bielski, Craig M; Donoghue, Mark T A; Gadiya, Mayur et al. (2018) Widespread Selection for Oncogenic Mutant Allele Imbalance in Cancer. Cancer Cell 34:852-862.e4
Chang, Matthew T; Bhattarai, Tripti Shrestha; Schram, Alison M et al. (2018) Accelerating Discovery of Functional Mutant Alleles in Cancer. Cancer Discov 8:174-183
Sabari, J K; Leonardi, G C; Shu, C A et al. (2018) PD-L1 expression, tumor mutational burden, and response to immunotherapy in patients with MET exon 14 altered lung cancers. Ann Oncol 29:2085-2091
Dunbar, Andrew; Nazir, Abbas; Levine, Ross (2017) Overview of Transgenic Mouse Models of Myeloproliferative Neoplasms (MPNs). Curr Protoc Pharmacol 77:14.40.1-14.40.19
Vardhana, Santosha A; Sauter, Craig S; Matasar, Matthew J et al. (2017) Outcomes of primary refractory diffuse large B-cell lymphoma (DLBCL) treated with salvage chemotherapy and intention to transplant in the rituximab era. Br J Haematol 176:591-599

Showing the most recent 10 out of 195 publications