Mantle cell lymphoma future or investigational therapies: Difference between revisions
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* In addition to the ongoing assessment of new monoclonal antibody-based therapies, the continued development of targeted molecular signaling inhibitors based on the underlying biology of MCL is an approach that will potentially yield fruitful results in this disease. | * In addition to the ongoing assessment of new monoclonal antibody-based therapies, the continued development of targeted molecular signaling inhibitors based on the underlying biology of MCL is an approach that will potentially yield fruitful results in this disease. | ||
* Some of the current therapies under clinical investigation are as follows: | * Some of the current therapies under clinical investigation are as follows: | ||
** Chimeric antigen receptor T-cell (CAR-T) therapy is being used in a phase II study of CAR-T therapy in relapsed MCL. | **BCL-2 inhibitor venetoclax (ABT-199) and the phosphatydilinosytol 3-kinase δ (PI3K δ) inhibitor idelalisib were tested in a phase I study and have shown promising results.<ref>{{Cite journal | ||
| author = [[Brad S. Kahl]], [[Stephen E. Spurgeon]], [[Richard R. Furman]], [[Ian W. Flinn]], [[Steven E. Coutre]], [[Jennifer R. Brown]], [[Don M. Benson]], [[John C. Byrd]], [[Sissy Peterman]], [[Yoonjin Cho]], [[Albert Yu]], [[Wayne R. Godfrey]] & [[Nina D. Wagner-Johnston]] | |||
| title = A phase 1 study of the PI3Kdelta inhibitor idelalisib in patients with relapsed/refractory mantle cell lymphoma (MCL) | |||
| journal = [[Blood]] | |||
| volume = 123 | |||
| issue = 22 | |||
| pages = 3398–3405 | |||
| year = 2014 | |||
| month = May | |||
| doi = 10.1182/blood-2013-11-537555 | |||
| pmid = 24615778 | |||
}}</ref><ref>{{Cite journal | |||
| author = [[Toby A. Eyre]], [[Harriet S. Walter]], [[Sunil Iyengar]], [[George Follows]], [[Matthew Cross]], [[Christopher P. Fox]], [[Andrew Hodson]], [[Josh Coats]], [[Santosh Narat]], [[Nick Morley]], [[Martin J. S. Dyer]] & [[Graham P. Collins]] | |||
| title = Efficacy of venetoclax monotherapy in patients with relapsed, refractory mantle cell lymphoma post BTK inhibitor therapy | |||
| journal = [[Haematologica]] | |||
| year = 2018 | |||
| month = September | |||
| doi = 10.3324/haematol.2018.198812 | |||
| pmid = 30190341 | |||
}}</ref> | |||
** Chimeric antigen receptor T-cell (CAR-T) therapy is being used in a phase II study of CAR-T therapy in relapsed MCL.<ref>{{Cite journal | |||
| author = [[James N. Kochenderfer]], [[Mark E. Dudley]], [[Sadik H. Kassim]], [[Robert P. T. Somerville]], [[Robert O. Carpenter]], [[Maryalice Stetler-Stevenson]], [[James C. Yang]], [[Giao Q. Phan]], [[Marybeth S. Hughes]], [[Richard M. Sherry]], [[Mark Raffeld]], [[Steven Feldman]], [[Lily Lu]], [[Yong F. Li]], [[Lien T. Ngo]], [[Andre Goy]], [[Tatyana Feldman]], [[David E. Spaner]], [[Michael L. Wang]], [[Clara C. Chen]], [[Sarah M. Kranick]], [[Avindra Nath]], [[Debbie-Ann N. Nathan]], [[Kathleen E. Morton]], [[Mary Ann Toomey]] & [[Steven A. Rosenberg]] | |||
| title = Chemotherapy-refractory diffuse large B-cell lymphoma and indolent B-cell malignancies can be effectively treated with autologous T cells expressing an anti-CD19 chimeric antigen receptor | |||
| journal = [[Journal of clinical oncology : official journal of the American Society of Clinical Oncology]] | |||
| volume = 33 | |||
| issue = 6 | |||
| pages = 540–549 | |||
| year = 2015 | |||
| month = February | |||
| doi = 10.1200/JCO.2014.56.2025 | |||
| pmid = 25154820 | |||
}}</ref> | |||
**Due to the male to female predominance of approximately 4:1 in MCL, investigators are investigating androgen receptor (AR) blockers like enzalutamide as means of decreasing MCL cell proliferation.<ref>{{Cite journal | |||
| author = [[Elahe A. Mostaghel]], [[Paul S. Martin]], [[Stephen Mongovin]], [[Shani Frayo]], [[Ailin Zhang]], [[Kerstin L. Edlefsen]], [[Oliver W. Press]] & [[Ajay K. Gopal]] | |||
| title = Androgen receptor expression in mantle cell lymphoma: Potential novel therapeutic implications | |||
| journal = [[Experimental hematology]] | |||
| volume = 49 | |||
| pages = 34–38 | |||
| year = 2017 | |||
| month = May | |||
| doi = 10.1016/j.exphem.2017.01.001 | |||
| pmid = 28115200 | |||
}}</ref> | |||
** | |||
*** | *** | ||
Revision as of 19:54, 12 December 2018
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Investigational therapies
- Recent advances in the understanding of the pathogenesis of mantle cell lymphoma has led to the development of targeted therapies which have shown potential promise as effective therapeutic approaches in the future..
- In addition to the ongoing assessment of new monoclonal antibody-based therapies, the continued development of targeted molecular signaling inhibitors based on the underlying biology of MCL is an approach that will potentially yield fruitful results in this disease.
- Some of the current therapies under clinical investigation are as follows:
- BCL-2 inhibitor venetoclax (ABT-199) and the phosphatydilinosytol 3-kinase δ (PI3K δ) inhibitor idelalisib were tested in a phase I study and have shown promising results.[1][2]
- Chimeric antigen receptor T-cell (CAR-T) therapy is being used in a phase II study of CAR-T therapy in relapsed MCL.[3]
- Due to the male to female predominance of approximately 4:1 in MCL, investigators are investigating androgen receptor (AR) blockers like enzalutamide as means of decreasing MCL cell proliferation.[4]
-
References
- ↑ Brad S. Kahl, Stephen E. Spurgeon, Richard R. Furman, Ian W. Flinn, Steven E. Coutre, Jennifer R. Brown, Don M. Benson, John C. Byrd, Sissy Peterman, Yoonjin Cho, Albert Yu, Wayne R. Godfrey & Nina D. Wagner-Johnston (2014). "A phase 1 study of the PI3Kdelta inhibitor idelalisib in patients with relapsed/refractory mantle cell lymphoma (MCL)". Blood. 123 (22): 3398–3405. doi:10.1182/blood-2013-11-537555. PMID 24615778. Unknown parameter
|month=
ignored (help) - ↑ Toby A. Eyre, Harriet S. Walter, Sunil Iyengar, George Follows, Matthew Cross, Christopher P. Fox, Andrew Hodson, Josh Coats, Santosh Narat, Nick Morley, Martin J. S. Dyer & Graham P. Collins (2018). "Efficacy of venetoclax monotherapy in patients with relapsed, refractory mantle cell lymphoma post BTK inhibitor therapy". Haematologica. doi:10.3324/haematol.2018.198812. PMID 30190341. Unknown parameter
|month=
ignored (help) - ↑ James N. Kochenderfer, Mark E. Dudley, Sadik H. Kassim, Robert P. T. Somerville, Robert O. Carpenter, Maryalice Stetler-Stevenson, James C. Yang, Giao Q. Phan, Marybeth S. Hughes, Richard M. Sherry, Mark Raffeld, Steven Feldman, Lily Lu, Yong F. Li, Lien T. Ngo, Andre Goy, Tatyana Feldman, David E. Spaner, Michael L. Wang, Clara C. Chen, Sarah M. Kranick, Avindra Nath, Debbie-Ann N. Nathan, Kathleen E. Morton, Mary Ann Toomey & Steven A. Rosenberg (2015). "Chemotherapy-refractory diffuse large B-cell lymphoma and indolent B-cell malignancies can be effectively treated with autologous T cells expressing an anti-CD19 chimeric antigen receptor". Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 33 (6): 540–549. doi:10.1200/JCO.2014.56.2025. PMID 25154820. Unknown parameter
|month=
ignored (help) - ↑ Elahe A. Mostaghel, Paul S. Martin, Stephen Mongovin, Shani Frayo, Ailin Zhang, Kerstin L. Edlefsen, Oliver W. Press & Ajay K. Gopal (2017). "Androgen receptor expression in mantle cell lymphoma: Potential novel therapeutic implications". Experimental hematology. 49: 34–38. doi:10.1016/j.exphem.2017.01.001. PMID 28115200. Unknown parameter
|month=
ignored (help)