Melanoma Clinical Trial
Official title:
Tumor Oximetry Using Electron Paramagnetic Resonance (EPR) With India Ink (Using Carbon Particulates From Carlo Erba [CE])
Verified date | December 2019 |
Source | Dartmouth-Hitchcock Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
It has been well established that malignant tumors tend to have low levels of oxygen and that
tumors with very low levels of oxygen are more resistant to radiotherapy and other
treatments, such as chemotherapy and immunotherapy. Previous attempts to improve response to
therapy by increasing the oxygen level of tissues have had disappointing results and
collectively have not led to changing clinical practice. Without a method to measure oxygen
levels in tumors or the ability to monitor over time whether tumors are responding to methods
to increase oxygen during therapy, clinician's reluctance to use oxygen therapy in usual
practice is not surprising.
The hypothesis underlying this research is that repeated measurements of tissue oxygen levels
can be used to optimize cancer therapy, including combined therapy, and to minimize normal
tissue side effects or complications. Because studies have found that tumors vary both in
their initial levels of oxygen and exhibit changing patterns during growth and treatment, we
propose to monitor oxygen levels in tumors and their responsiveness to hyperoxygenation
procedures. Such knowledge about oxygen levels in tumor tissues and their responsiveness to
hyper-oxygenation could potentially be used to select subjects for particular types of
treatment, or otherwise to adjust routine care for patients known to have hypoxic but
unresponsive tumors in order to improve their outcomes.
The overall objectives of this study are to establish the clinical feasibility and efficacy
of using in vivo electron paramagnetic resonance (EPR) oximetry—a technique related to
magnetic resonance imaging (MRI)—to obtain direct and repeated measurements of clinically
useful information about tumor tissue oxygenation in specific groups of subjects with the
same types of tumors, and to establish the clinical feasibility and efficacy of using
inhalation of enriched oxygen to gain additional clinically useful information about
responsiveness of tumors to hyper-oxygenation. Two devices are used: a paramagnetic charcoal
suspension (Carlo Erba India ink) and in vivo EPR oximetry to assess oxygen levels. The ink
is injected and becomes permanent in the tissue at the site of injection unless removed;
thereafter, the in vivo oximetry measurements are noninvasive and can be repeated
indefinitely.
Status | Terminated |
Enrollment | 3 |
Est. completion date | October 27, 2019 |
Est. primary completion date | October 27, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Subject must be capable of giving informed consent or has an acceptable surrogate capable of giving consent on behalf of the subject. 2. Subject has an eligible tumor that is within 5 mm of the surface (either skin or mucosa) or has had a tumor removed with a tumor bed that is within 5 mm of the surface. 1. Eligible tumors types: - Intraoral tumors: squamous cell carcinoma (SCC), melanoma; - Primary cutaneous tumors (including, but not limited to): SCC, basal cell carcinoma (BCC,) melanoma; - Breast malignancies post surgery; - Other tumors: any tumor within 5 mm of the surface and with planned radiation therapy. Exclusion Criteria: 1. Previous adverse reaction to a charcoal product e.g., a local hypersensitive response from a black tattoo or from ingestion of activated charcoal 2. Previous adverse reaction to the suspending agent 3. Subject has a pacemaker that is not known to be MRI compatible 4. Subject has a non-removable implant or device with metal that is not known to be MRI compatible 5. Subject is pregnant or has a likelihood for becoming pregnant during the basic study timeframe. Note: There is no known harm to the woman or her fetus from participating; this is precautionary only. |
Country | Name | City | State |
---|---|---|---|
United States | Dartmouth-Hitchcock Medical Center | Lebanon | New Hampshire |
Lead Sponsor | Collaborator |
---|---|
Philip Schaner | National Cancer Institute (NCI) |
United States,
Bacic G, Liu KJ, O'Hara JA, Harris RD, Szybinski K, Goda F, Swartz HM. Oxygen tension in a murine tumor: a combined EPR and MRI study. Magn Reson Med. 1993 Nov;30(5):568-72. — View Citation
Baudelet C, Gallez B. How does blood oxygen level-dependent (BOLD) contrast correlate with oxygen partial pressure (pO2) inside tumors? Magn Reson Med. 2002 Dec;48(6):980-6. — View Citation
Brizel DM, Scully SP, Harrelson JM, Layfield LJ, Dodge RK, Charles HC, Samulski TV, Prosnitz LR, Dewhirst MW. Radiation therapy and hyperthermia improve the oxygenation of human soft tissue sarcomas. Cancer Res. 1996 Dec 1;56(23):5347-50. — View Citation
Brizel DM, Sibley GS, Prosnitz LR, Scher RL, Dewhirst MW. Tumor hypoxia adversely affects the prognosis of carcinoma of the head and neck. Int J Radiat Oncol Biol Phys. 1997 May 1;38(2):285-9. — View Citation
Chaplin DJ, Horsman MR. Tumor blood flow changes induced by chemical modifiers of radiation response. Int J Radiat Oncol Biol Phys. 1992;22(3):459-62. — View Citation
Charlier N, Beghein N, Gallez B. Development and evaluation of biocompatible inks for the local measurement of oxygen using in vivo EPR. NMR Biomed. 2004 Aug;17(5):303-10. — View Citation
Dardzinski BJ, Sotak CH. Rapid tissue oxygen tension mapping using 19F inversion-recovery echo-planar imaging of perfluoro-15-crown-5-ether. Magn Reson Med. 1994 Jul;32(1):88-97. — View Citation
Demidenko E. Mixed models: theory and applications with R. John Wiley & Sons; 2013 Aug 26.
Dewhirst MW, Poulson JM, Yu D, Sanders L, Lora-Michiels M, Vujaskovic Z, Jones EL, Samulski TV, Powers BE, Brizel DM, Prosnitz LR, Charles HC. Relation between pO2, 31P magnetic resonance spectroscopy parameters and treatment outcome in patients with high-grade soft tissue sarcomas treated with thermoradiotherapy. Int J Radiat Oncol Biol Phys. 2005 Feb 1;61(2):480-91. — View Citation
Dunn JF, Ding S, O'Hara JA, Liu KJ, Rhodes E, Weaver JB, Swartz HM. The apparent diffusion constant measured by MRI correlates with pO2 in a RIF-1 tumor. Magn Reson Med. 1995 Oct;34(4):515-9. — View Citation
Flood AB, Satinsky VA, Swartz HM. Comparing the Effectiveness of Methods to Measure Oxygen in Tissues for Prognosis and Treatment of Cancer. Adv Exp Med Biol. 2016;923:113-120. doi: 10.1007/978-3-319-38810-6_15. Review. — View Citation
Gallez B, Baudelet C, Jordan BF. Assessment of tumor oxygenation by electron paramagnetic resonance: principles and applications. NMR Biomed. 2004 Aug;17(5):240-62. Review. — View Citation
Gallez B, Debuyst R, Dejehet F, Liu KJ, Walczak T, Goda F, Demeure R, Taper H, Swartz HM. Small particles of fusinite and carbohydrate chars coated with aqueous soluble polymers: preparation and applications for in vivo EPR oximetry. Magn Reson Med. 1998 Jul;40(1):152-9. — View Citation
Gallez B, Swartz HM. In vivo EPR: when, how and why? NMR Biomed. 2004 Aug;17(5):223-5. — View Citation
Gatenby RA, Kessler HB, Rosenblum JS, Coia LR, Moldofsky PJ, Hartz WH, Broder GJ. Oxygen distribution in squamous cell carcinoma metastases and its relationship to outcome of radiation therapy. Int J Radiat Oncol Biol Phys. 1988 May;14(5):831-8. — View Citation
Glockner JF, Norby SW, Swartz HM. Simultaneous measurement of intracellular and extracellular oxygen concentrations using a nitroxide-liposome system. Magn Reson Med. 1993 Jan;29(1):12-8. — View Citation
Glockner JF, Swartz HM. In vivo EPR oximetry using two novel probes: fusinite and lithium phthalocyanine. Adv Exp Med Biol. 1992;317:229-34. — View Citation
Goda F, Liu KJ, Walczak T, O'Hara JA, Jiang J, Swartz HM. In vivo oximetry using EPR and India ink. Magn Reson Med. 1995 Feb;33(2):237-45. — View Citation
Goda F, O'Hara JA, Liu KJ, Rhodes ES, Dunn JF, Swartz HM. Comparisons of measurements of pO2 in tissue in vivo by EPR oximetry and microelectrodes. Adv Exp Med Biol. 1997;411:543-9. — View Citation
Goda F, O'Hara JA, Rhodes ES, Liu KJ, Dunn JF, Bacic G, Swartz HM. Changes of oxygen tension in experimental tumors after a single dose of X-ray irradiation. Cancer Res. 1995 Jun 1;55(11):2249-52. — View Citation
Haga T, Hirata H, Lesniewski P, Rychert KM, Williams BB, Flood AN, Swartz HM. L-band surface-coil resonator with voltage-control impedance-matching for EPR tooth dosimetry. Concepts in Magnetic Resonance Part B: Magnetic Resonance Engineering. 2013 Feb 1;43(1):32-40.2013).
Hall EJ, Giaccia AJ. Radiobiology for the Radiologist. Philadelphia: JB Lippincott. 1988.
Hees PS, Sotak CH. Assessment of changes in murine tumor oxygenation in response to nicotinamide using 19F NMR relaxometry of a perfluorocarbon emulsion. Magn Reson Med. 1993 Mar;29(3):303-10. Erratum in: Magn Reson Med 1993 May;29(5):716. — View Citation
Hirata H, Walczak T, Swartz HM. Electronically tunable surface-coil-type resonator for L-band EPR spectroscopy. J Magn Reson. 2000 Jan;142(1):159-67. — View Citation
Höckel M, Schlenger K, Mitze M, Schäffer U, Vaupel P. Hypoxia and Radiation Response in Human Tumors. Semin Radiat Oncol. 1996 Jan;6(1):3-9. — View Citation
Höckel M, Vorndran B, Schlenger K, Baussmann E, Knapstein PG. Tumor oxygenation: a new predictive parameter in locally advanced cancer of the uterine cervix. Gynecol Oncol. 1993 Nov;51(2):141-9. — View Citation
Hyde JS and Subczynski, WK. Spin-label oximetry. (1989). Pp 399-425. In: Berliner LJ, Reuben J (ed). Spin Labeling: Theory and Applications. New York: Plenum Press. doi: 10.1007/978-1-4613-0743-3_8
Islam PS, Chang C, Selmi C, Generali E, Huntley A, Teuber SS, Gershwin ME. Medical Complications of Tattoos: A Comprehensive Review. Clin Rev Allergy Immunol. 2016 Apr;50(2):273-86. doi: 10.1007/s12016-016-8532-0. Review. — View Citation
Jordan BF, Baudelet C, Gallez B. Carbon-centered radicals as oxygen sensors for in vivo electron paramagnetic resonance: screening for an optimal probe among commercially available charcoals. MAGMA. 1998 Dec;7(2):121-9. — View Citation
Jordan BF, Grégoire V, Demeure RJ, Sonveaux P, Feron O, O'Hara J, Vanhulle VP, Delzenne N, Gallez B. Insulin increases the sensitivity of tumors to irradiation: involvement of an increase in tumor oxygenation mediated by a nitric oxide-dependent decrease of the tumor cells oxygen consumption. Cancer Res. 2002 Jun 15;62(12):3555-61. — View Citation
Jordan BF, Misson P, Demeure R, Baudelet C, Beghein N, Gallez B. Changes in tumor oxygenation/perfusion induced by the no donor, isosorbide dinitrate, in comparison with carbogen: monitoring by EPR and MRI. Int J Radiat Oncol Biol Phys. 2000 Sep 1;48(2):565-70. — View Citation
Jordan BF, Sonveaux P, Feron O, Grégoire V, Beghein N, Gallez B. Nitric oxide-mediated increase in tumor blood flow and oxygenation of tumors implanted in muscles stimulated by electric pulses. Int J Radiat Oncol Biol Phys. 2003 Mar 15;55(4):1066-73. — View Citation
Khan N, Grinberg O, Wilmot C, Kiefer H, Swartz HM. "Distant spin trapping": a method for expanding the availability of spin trapping measurements. J Biochem Biophys Methods. 2005 Feb 28;62(2):125-30. Epub 2004 Nov 13. — View Citation
Lartigau E, Lusinchi A, Eschwege F, Guichard M. Tumor oxygenation: the Institut Gustave Roussy experience. In: Vaupel P, Kelleher DK (ed). Tumor hypoxia pathophysiology, clinical significance and therapeutic perspectives. Stuttgart, Germany: Wissenschaftliche Verlagsgesellschaft mbH. 1999:47-52.
Lartigau E, Randrianarivelo H, Avril MF, Margulis A, Spatz A, Eschwège F, Guichard M. Intratumoral oxygen tension in metastatic melanoma. Melanoma Res. 1997 Oct;7(5):400-6. — View Citation
Liu KJ, Gast P, Moussavi M, Norby SW, Vahidi N, Walczak T, Wu M, Swartz HM. Lithium phthalocyanine: a probe for electron paramagnetic resonance oximetry in viable biological systems. Proc Natl Acad Sci U S A. 1993 Jun 15;90(12):5438-42. — View Citation
Nakashima T, Jiang J, Goda F, Shima T, Swartz HM. The measurement of pO2 in mouse liver in vivo by EPR oximetry using india ink. Magn. Reson. Med. 1995;6:158-60.
Nilges MJ, Walczak T, Swartz HM. GHz in vivo ESR spectrometer operating with a surface probe. Phys. Med. 1989;5:195-201.
Nordsmark M, Alsner J, Keller J, Nielsen OS, Jensen OM, Horsman MR, Overgaard J. Hypoxia in human soft tissue sarcomas: adverse impact on survival and no association with p53 mutations. Br J Cancer. 2001 Apr 20;84(8):1070-5. — View Citation
Nordsmark M, Bentzen SM, Rudat V, Brizel D, Lartigau E, Stadler P, Becker A, Adam M, Molls M, Dunst J, Terris DJ, Overgaard J. Prognostic value of tumor oxygenation in 397 head and neck tumors after primary radiation therapy. An international multi-center study. Radiother Oncol. 2005 Oct;77(1):18-24. Epub 2005 Aug 10. — View Citation
O'Hara JA, Goda F, Demidenko E, Swartz HM. Effect on regrowth delay in a murine tumor of scheduling split-dose irradiation based on direct pO2 measurements by electron paramagnetic resonance oximetry. Radiat Res. 1998 Nov;150(5):549-56. — View Citation
O'Hara JA, Goda F, Liu KJ, Bacic G, Hoopes PJ, Swartz HM. The pO2 in a murine tumor after irradiation: an in vivo electron paramagnetic resonance oximetry study. Radiat Res. 1995 Nov;144(2):222-9. — View Citation
O'Hara JA, Hou H, Demidenko E, Springett RJ, Khan N, Swartz HM. Simultaneous measurement of rat brain cortex PtO2 using EPR oximetry and a fluorescence fiber-optic sensor during normoxia and hyperoxia. Physiol Meas. 2005 Jun;26(3):203-13. Epub 2005 Feb 25. — View Citation
O'Hara JA, Khan N, Hou H, Wilmo CM, Demidenko E, Dunn JF, Swartz HM. Comparison of EPR oximetry and Eppendorf polarographic electrode assessments of rat brain PtO2. Physiol Meas. 2004 Dec;25(6):1413-23. — View Citation
Petryakov SV, Schreiber W, Kmiec MM, Williams BB, Swartz HM. Surface Dielectric Resonators for X-band EPR Spectroscopy. Radiat Prot Dosimetry. 2016 Dec;172(1-3):127-132. doi: 10.1093/rpd/ncw167. Epub 2016 Jul 15. — View Citation
Salikhov I, Hirata H, Walczak T, Swartz HM. An improved external loop resonator for in vivo L-band EPR spectroscopy. J Magn Reson. 2003 Sep;164(1):54-9. — View Citation
Salikhov IK, Swartz HM. Measurement of specific absorption rate for clinical EPR at 1200 MHz. Applied Magnetic Resonance. 2005 Jun 1;29(2):287-91.
Smirnov AI, Norby SW, Clarkson RB, Walczak T, Swartz HM. Simultaneous multi-site EPR spectroscopy in vivo. Magn Reson Med. 1993 Aug;30(2):213-20. — View Citation
Smirnov AI, Norby SW, Walczak T, Liu KJ, Swartz HM. Physical and instrumental considerations in the use of lithium phthalocyanine for measurements of the concentration of the oxygen. J Magn Reson B. 1994 Feb;103(2):95-102. — View Citation
Swartz HM, Clarkson RB. The measurement of oxygen in vivo using EPR techniques. Phys Med Biol. 1998 Jul;43(7):1957-75. Review. — View Citation
Swartz HM, Dunn J, Grinberg O, O'Hara J, Walczak T. What does EPR oximetry with solid particles measure--and how does this relate to other measures of PO2? Adv Exp Med Biol. 1997;428:663-70. — View Citation
Swartz HM, Dunn JF. Measurements of oxygen in tissues: overview and perspectives on methods. Adv Exp Med Biol. 2003;530:1-12. Review. — View Citation
Swartz HM, Halpern H. EPR studies of living animals and related model systems (in vivo EPR). InBiological magnetic resonance 2002 (pp. 367-404). Springer US.
Swartz HM, Hou H, Khan N, Jarvis LA, Chen EY, Williams BB, Kuppusamy P. Advances in probes and methods for clinical EPR oximetry. Adv Exp Med Biol. 2014;812:73-79. doi: 10.1007/978-1-4939-0620-8_10. Review. — View Citation
Swartz HM, Iwasaki A, Walczak T, Demidenko E, Salikov I, Lesniewski P, Starewicz P, Schauer D, Romanyukha A. Measurements of clinically significant doses of ionizing radiation using non-invasive in vivo EPR spectroscopy of teeth in situ. Appl Radiat Isot. 2005 Feb;62(2):293-9. — View Citation
Swartz HM, Khan N, Buckey J, Comi R, Gould L, Grinberg O, Hartford A, Hopf H, Hou H, Hug E, Iwasaki A, Lesniewski P, Salikhov I, Walczak T. Clinical applications of EPR: overview and perspectives. NMR Biomed. 2004 Aug;17(5):335-51. Review. — View Citation
Swartz HM, Liu KJ, Goda F, Walczak T. India ink: a potential clinically applicable EPR oximetry probe. Magn Reson Med. 1994 Feb;31(2):229-32. — View Citation
Swartz HM, Williams BB, Hou H, Khan N, Jarvis LA, Chen EY, Schaner PE, Ali A, Gallez B, Kuppusamy P, Flood AB. Direct and Repeated Clinical Measurements of pO2 for Enhancing Cancer Therapy and Other Applications. Adv Exp Med Biol. 2016;923:95-104. doi: 10.1007/978-3-319-38810-6_13. — View Citation
Swartz HM, Williams BB, Jarvis LA, Zaki BI, Gladstone DJ. Repeated monitoring of tumor oxygen while breathing carbogen to determine the therapeutic potential of hyperoxic therapy. Pract Radiat Oncol. 2013 Apr-Jun;3(2 Suppl 1):S23-4. doi: 10.1016/j.prro.2013.01.084. Epub 2013 Mar 25. — View Citation
Swartz HM, Williams BB, Zaki BI, Hartford AC, Jarvis LA, Chen EY, Comi RJ, Ernstoff MS, Hou H, Khan N, Swarts SG, Flood AB, Kuppusamy P. Clinical EPR: unique opportunities and some challenges. Acad Radiol. 2014 Feb;21(2):197-206. doi: 10.1016/j.acra.2013.10.011. Review. — View Citation
Swartz HM. EPR Studies of Cells and Tissue. In: Foundations Of Modern EPR 1998 (pp. 451-459).
Swartz HM. Potential Medical (Clinical) Applications of EPR: Overview & Perspectives. InIn Vivo EPR (ESR) 2003 (pp. 599-621). Springer US.
Swartz HM. Using EPR to measure a critical but often unmeasured component of oxidative damage: oxygen. Antioxid Redox Signal. 2004 Jun;6(3):677-86. Review. — View Citation
Swartz, HM, N. Khan, B.B. Williams, A.C. Hartford, B. Zaki, M. Ernstoff, J.C. Buckey, F.F. Gubaidullin, H. Hou, P. Lesniewski, M. Kmiec, O.Y. Grinberg, A. Sucheta, and T. Walczak, Clinical Applications of In Vivo EPR: EPR Oximetry in Treasures of Eureka, Electron Paramagnetic Resonance From Fundamental Research To Pioneering Applications & Zavoisky Award, Volume 1, Axas Publishing, New Zealand, pp. 178-179 (2009).
Swartz, HM, R.P. Mason, N. Hogg, B. Kalyanaraman, T. Sarna, P.M. Plonka, M. Zareb, P.L. Gutierrez, and L.J. Berliner, Free Radicals and Medicine, in Biomedical ESR a volume in the Biological Magnetic Resonance Series (S.S. Eaton, G.R. Eaton, L.J. Berliner, eds.), Kluwer Publisher (The Netherlands, New York, Boston), Chapter 3, pp. 25-74 (2004a).
Tremper KK, Friedman AE, Levine EM, Lapin R, Camarillo D. The preoperative treatment of severely anemic patients with a perfluorochemical oxygen-transport fluid, Fluosol-DA. N Engl J Med. 1982 Jul 29;307(5):277-83. — View Citation
Vaeth JM. Hyperbaric oxygen and radiation therapy of cancer. Frontiers of Radiation Therapy and Oncology. 1: 195 (1968).
Vahidi N, Clarkson RB, Liu KJ, Norby SW, Wu M, Swartz HM. In vivo and in vitro EPR oximetry with fusinite: a new coal-derived, particulate EPR probe. Magn Reson Med. 1994 Feb;31(2):139-46. — View Citation
Vaupel P, Höckel M, Mayer A. Detection and characterization of tumor hypoxia using pO2 histography. Antioxid Redox Signal. 2007 Aug;9(8):1221-35. Review. — View Citation
Vaupel P. Tumor microenvironmental physiology and its implications for radiation oncology. Semin Radiat Oncol. 2004 Jul;14(3):198-206. Review. — View Citation
Williams BB, Khan N, Zaki B, Hartford A, Ernstoff MS, Swartz HM. Clinical electron paramagnetic resonance (EPR) oximetry using India ink. Adv Exp Med Biol. 2010;662:149-56. doi: 10.1007/978-1-4419-1241-1_21. — View Citation
* Note: There are 71 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Tissue Histology | For those subjects whose tumor is resected along with the tissue containing the India ink carbon particles as a part of their usual care, the tissue at the site of the injection will be submitted for processing with standard pathology procedures. Tissue sections spanning the injection site(s) will be evaluated for the extent and mechanism of dispersion and for the presence of acute or chronic inflammation or other tissue reaction (scar, fibrosis, capsule formation, or other). The tissue will be assessed as to whether the reaction observed is as expected for ink injections. | Approximately 30 days post-surgical excision of the tumor | |
Primary | Measurement of oxygen levels in tissues in response to hyperoxic therapy | This study will assess whether the addition of hyperoxic therapy (100% oxygen delivered through a non-rebreather face mask) will increase the oxygen level of a tumor or tumor bed by > 5 mm Hg using EPR oximetry. Tumor oxygen values will be reported in millimeters of mercury (mmHg). | From time of ink injection to the time the ink is removed through surgical resection. This can range from days to years, or until the study's completion of enrollment, anticipated in 2020. | |
Secondary | Characterize oxygen changes in tumor beds throughout the course of radiation therapy | This outcome will measure oxygen in the post-surgical tissue throughout the course of radiation therapy using EPR oximetry. Tissue oxygen values will be reported in millimeters of mercury (mmHg). | From time of ink injection through the completion of radiation therapy; an average of 4 months. | |
Secondary | Characterize oxygen changes in tumors throughout the course of radiation therapy | This outcome will measure tumor tissue oxygen throughout the course of radiation therapy using EPR oximetry. Tissue oxygen values will be reported in millimeters of mercury (mmHg). | From time of ink injection through the completion of radiation therapy; an average of 4 months. | |
Secondary | Characterize oxygen changes in tumor and tumor beds prior to radiation therapy | For those subjects receiving India ink injections in both the untreated tumor and in the post-surgical bed prior to radiation, we will examine patterns across these two 'states' in individual tumors, which can enhance our understanding of the relationship between the oxygen levels in the tumor and in the resulting tumor bed. Tissue oxygen values will be reported in millimeters of mercury (mmHg). | From time of ink injection through the completion of medical treatment for cancer; an average of 4 months. | |
Secondary | Characterize oxygen changes in tumor and tumor beds through the course of radiation therapy | For those subjects receiving India ink injections in both the untreated tumor and in the post-surgical bed while undergoing radiation therapy, we will examine patterns across these two 'states' in individual tumors, which can enhance our understanding of the relationship between the oxygen levels in the tumor and in the resulting tumor bed. Tissue oxygen values will be reported in millimeters of mercury (mmHg). | From time of ink injection through the completion of medical treatment for cancer; an average of 6 months. |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05094804 -
A Study of OR2805, a Monoclonal Antibody Targeting CD163, Alone and in Combination With Anticancer Agents
|
Phase 1/Phase 2 | |
Completed |
NCT03979872 -
Risk Information and Skin-cancer Education for Undergraduate Prevention
|
N/A | |
Recruiting |
NCT04986748 -
Using QPOP to Predict Treatment for Sarcomas and Melanomas
|
||
Enrolling by invitation |
NCT00068003 -
Harvesting Cells for Experimental Cancer Treatments
|
||
Recruiting |
NCT05707286 -
Pilot Study to Determine Pro-Inflammatory Cytokine Kinetics During Immune Checkpoint Inhibitor Therapy
|
||
Active, not recruiting |
NCT05470283 -
Phase I, Open-Label, Study of Tumor Infiltrating Lymphocytes Engineered With Membrane Bound IL15 Plus Acetazolamide in Adult Patients With Metastatic Melanoma
|
Phase 1 | |
Recruiting |
NCT05077137 -
A Feasibility Study Utilizing Immune Recall to Increase Response to Checkpoint Therapy
|
Phase 1 | |
Active, not recruiting |
NCT02721459 -
XL888 + Vemurafenib + Cobimetinib for Unresectable BRAF Mutated Stage III/IV Melanoma
|
Phase 1 | |
Completed |
NCT00341939 -
Retrospective Analysis of a Drug-Metabolizing Genotype in Cancer Patients and Correlation With Pharmacokinetic and Pharmacodynamics Data
|
||
Recruiting |
NCT05839912 -
Excision of Lymph Node Trial (EXCILYNT) (Mel69)
|
N/A | |
Recruiting |
NCT04971499 -
A Study of Dapansutrile Plus Pembrolizumab in Patients With PD-1 Refractory Advanced Melanoma
|
Phase 1/Phase 2 | |
Recruiting |
NCT05263453 -
HL-085+Vemurafenib to Treat Advanced Melanoma Patients With BRAF V600E/K Mutation
|
Phase 2 | |
Active, not recruiting |
NCT05060432 -
Study of EOS-448 With Standard of Care and/or Investigational Therapies in Participants With Advanced Solid Tumors
|
Phase 1/Phase 2 | |
Not yet recruiting |
NCT06413680 -
A First-In Human (FIH) Trial to Find Out if REGN10597 is Safe and How Well it Works for Adult Participants With Advanced Solid Organ Malignancies
|
Phase 1/Phase 2 | |
Completed |
NCT03348891 -
TNF in Melanoma Patients Treated With Immunotherapy
|
N/A | |
Terminated |
NCT03399448 -
NY-ESO-1-redirected CRISPR (TCRendo and PD1) Edited T Cells (NYCE T Cells)
|
Phase 1 | |
Completed |
NCT03171064 -
Exercise as a Supportive Measure for Patients Undergoing Checkpoint-inhibitor Treatment
|
Phase 2 | |
Not yet recruiting |
NCT05539118 -
Interferon-α1b Combined With Toripalimab and Anlotinib Hydrochloride in Advanced Unresectable Melanoma
|
Phase 1/Phase 2 | |
Recruiting |
NCT05171374 -
pRospective Evaluation of Clinical Outcomes in Patients With metAsTatIс melanOma Treated With dabrafeNib and trAmetinib in reaL practicE
|
||
Withdrawn |
NCT02854488 -
Yervoy Pregnancy Surveillance Study
|