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Boronophenylalanine (BPA)-Based Boron Neutron Capture Therapy (BNCT) in the Treatment Head and Neck Tumors

Primary Purpose

Head and Neck Cancer

Status
Completed
Phase
Phase 1
Locations
Finland
Study Type
Interventional
Intervention
boronophenylalanine-based BNCT
Sponsored by
Boneca Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Head and Neck Cancer focused on measuring head and neck cancer, boron neutron capture therapy, radiation therapy, boronophenylalanine

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Histologically confirmed, malignant head and neck cancer. Inoperable tumor, prior surgery may or may not have been done. Prior radiotherapy or chemoradiotherapy has been given. If prior SPECT or PET with 18F-BFA has been done, BPA needs to accumulate at least 2.5 times more in the tumor than in the corresponding contralateral normal tissue. WHO performance status <3. WBC >2,500/mm3, platelets >75,000/mm3, serum creatinine <180 umol/L. A written informed consent. Exclusion Criteria: Lymphoma or other tumor type that is expected to respond to cancer chemotherapy or to a dose of conventional radiation therapy that can be safely given. A non-experimental, effective treatment option is available. Expected survival less than 3 months. Concomitant systemic chemotherapy (prior cancer chemotherapy is allowed). Other concurrent experimental therapy, or such therapy is being planned to be given. Less than 3 months since prior radiation therapy. Untreated or severe, treated congestive heart failure or renal failure. A cardiac pace-maker or an unremovable metal implant present in the head and neck region that will interfere with MRI-based dose-planning. Restlessness or inability to lie in a cast for 30 to 60 minutes. Clinical follow-up after therapy cannot be arranged or the patient is not willing to participate in follow-up. Pregnancy. Age less than 18. The patient is not able to understand the treatment options.

Sites / Locations

  • Department of Oncology, Helsinki University Central Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

BNCT.

Arm Description

Boronophenylalanine-based BNCT.

Outcomes

Primary Outcome Measures

treatment response

Secondary Outcome Measures

time to progression
safety

Full Information

First Posted
June 17, 2005
Last Updated
May 3, 2013
Sponsor
Boneca Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT00114790
Brief Title
Boronophenylalanine (BPA)-Based Boron Neutron Capture Therapy (BNCT) in the Treatment Head and Neck Tumors
Official Title
Boronophenylalanine (BPA)-Based Boron Neutron Capture Therapy (BNCT) in the Treatment of Inoperable and Irradiated Head and Neck Tumors: A Feasibility Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2013
Overall Recruitment Status
Completed
Study Start Date
December 2003 (undefined)
Primary Completion Date
October 2008 (Actual)
Study Completion Date
January 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Boneca Corporation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Boron Neutron Capture Therapy (BNCT) is an experimental radiation therapy technique which is based on the principle of irradiating boron atoms with neutrons. When neutrons have relatively low energy, boron atoms that have been targeted to cancerous tissue using a suitable boron carrier (an amino acid derivative called BPA, boronophenylalanine) will capture the neutrons. As a result from the neutron capture the boron atoms will split into two, producing helium and lithium ions. The helium and lithium ions, in turn, have only a short pathlength in tissue (about 5 micrometers) and will deposit their cell damaging effect mainly within the tumor provided that the boron carrier (BPA) has accumulated in the tumor. In practice, the study participants will receive BPA as an approximately 2-hour intravenous infusion, following which the tumor is irradiated with low energy (epithermal) neutrons obtained from a nuclear reactor at the BNCT facility. BNCT requires careful radiation dose planning, but neutron irradiation will last approximately only for one hour. In this study BNCT will be repeated, and the 2 treatments will be given 3 to 5 weeks apart. The study hypothesis is that head and neck cancers that have recurred following conventional radiotherapy might accumulate the boron carrier compound, and might respond to BNCT.
Detailed Description
This is a single BNCT-facility, non-randomized, non-comparative, open-label, phase I to II trial to determine the value of BNCT in the treatment of inoperable, irradiated, locally advanced cancers of the head and neck region. An attempt to perform 18F-labeled boronophenylalanine (18F-BPA) SPECT or PET imaging will be made before BNCT. Patients whose tumor uptake is >2.5 times that of the corresponding normal head and neck tissue will be enrolled, and treated with a single fraction BPA-based BNCT twice, 3 to 5 weeks apart. Another 18F-BPA SPECT or PET study may be performed 1 to 3 months after BNCT to determine the SPECT/PET response. The neutron irradiation site is the FiR 1 reactor site, located at Otaniemi, Espoo, Finland, about 6 kilometers from the Helsinki University Central Hospital, Helsinki, where patient evaluation and post-irradiation care will take place. Prior to BNCT, BPA is infused as a fructose complex (l-BPA-F) into a peripheral vein over 2 hours. Blood samples will be taken for monitoring whole blood boron concentration before starting the BPA infusion, and thereafter at 20 to 40 minute intervals during the infusion, following infusion, and after delivering neutron irradiation. The blood samples will be analyzed for blood boron concentration to estimate the average blood boron concentration during neutron irradiation. All patients will be evaluated for response using CT or magnetic resonance imaging (MRI).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Head and Neck Cancer
Keywords
head and neck cancer, boron neutron capture therapy, radiation therapy, boronophenylalanine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
BNCT.
Arm Type
Experimental
Arm Description
Boronophenylalanine-based BNCT.
Intervention Type
Radiation
Intervention Name(s)
boronophenylalanine-based BNCT
Intervention Description
Boronophenylalanine is infused into a peripheral vein prior to neutron irradiation.
Primary Outcome Measure Information:
Title
treatment response
Time Frame
1 year
Secondary Outcome Measure Information:
Title
time to progression
Time Frame
2 years
Title
safety
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically confirmed, malignant head and neck cancer. Inoperable tumor, prior surgery may or may not have been done. Prior radiotherapy or chemoradiotherapy has been given. If prior SPECT or PET with 18F-BFA has been done, BPA needs to accumulate at least 2.5 times more in the tumor than in the corresponding contralateral normal tissue. WHO performance status <3. WBC >2,500/mm3, platelets >75,000/mm3, serum creatinine <180 umol/L. A written informed consent. Exclusion Criteria: Lymphoma or other tumor type that is expected to respond to cancer chemotherapy or to a dose of conventional radiation therapy that can be safely given. A non-experimental, effective treatment option is available. Expected survival less than 3 months. Concomitant systemic chemotherapy (prior cancer chemotherapy is allowed). Other concurrent experimental therapy, or such therapy is being planned to be given. Less than 3 months since prior radiation therapy. Untreated or severe, treated congestive heart failure or renal failure. A cardiac pace-maker or an unremovable metal implant present in the head and neck region that will interfere with MRI-based dose-planning. Restlessness or inability to lie in a cast for 30 to 60 minutes. Clinical follow-up after therapy cannot be arranged or the patient is not willing to participate in follow-up. Pregnancy. Age less than 18. The patient is not able to understand the treatment options.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heikki T Joensuu, M.D., prof.
Organizational Affiliation
Helsinki University Central Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Oncology, Helsinki University Central Hospital
City
Helsinki
ZIP/Postal Code
FIN-00029
Country
Finland

12. IPD Sharing Statement

Citations:
PubMed Identifier
15236879
Citation
Kouri M, Kankaanranta L, Seppala T, Tervo L, Rasilainen M, Minn H, Eskola O, Vahatalo J, Paetau A, Savolainen S, Auterinen I, Jaaskelainen J, Joensuu H. Undifferentiated sinonasal carcinoma may respond to single-fraction boron neutron capture therapy. Radiother Oncol. 2004 Jul;72(1):83-5. doi: 10.1016/j.radonc.2004.03.016.
Results Reference
background
PubMed Identifier
12749708
Citation
Joensuu H, Kankaanranta L, Seppala T, Auterinen I, Kallio M, Kulvik M, Laakso J, Vahatalo J, Kortesniemi M, Kotiluoto P, Seren T, Karila J, Brander A, Jarviluoma E, Ryynanen P, Paetau A, Ruokonen I, Minn H, Tenhunen M, Jaaskelainen J, Farkkila M, Savolainen S. Boron neutron capture therapy of brain tumors: clinical trials at the finnish facility using boronophenylalanine. J Neurooncol. 2003 Mar-Apr;62(1-2):123-34. doi: 10.1007/BF02699939.
Results Reference
background
PubMed Identifier
36269660
Citation
Porra L, Wendland L, Seppala T, Koivunoro H, Revitzer H, Tervonen J, Kankaanranta L, Anttonen A, Tenhunen M, Joensuu H. From Nuclear Reactor-Based to Proton Accelerator-Based Therapy: The Finnish Boron Neutron Capture Therapy Experience. Cancer Biother Radiopharm. 2023 Apr;38(3):184-191. doi: 10.1089/cbr.2022.0059. Epub 2022 Oct 21.
Results Reference
derived
PubMed Identifier
21300462
Citation
Kankaanranta L, Seppala T, Koivunoro H, Saarilahti K, Atula T, Collan J, Salli E, Kortesniemi M, Uusi-Simola J, Valimaki P, Makitie A, Seppanen M, Minn H, Revitzer H, Kouri M, Kotiluoto P, Seren T, Auterinen I, Savolainen S, Joensuu H. Boron neutron capture therapy in the treatment of locally recurred head-and-neck cancer: final analysis of a phase I/II trial. Int J Radiat Oncol Biol Phys. 2012 Jan 1;82(1):e67-75. doi: 10.1016/j.ijrobp.2010.09.057. Epub 2011 Feb 6.
Results Reference
derived
Links:
URL
http://www.boneca.fi
Description
Boneca Corporation is a Finnish company that provides BNCT.

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Boronophenylalanine (BPA)-Based Boron Neutron Capture Therapy (BNCT) in the Treatment Head and Neck Tumors

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