Paraneoplastic Syndrome

This trial studies neuroendocrine tumors, paraganglioma, pheochromocytoma, and other SSTR-positive tumors that are not currently approved for lutetium therapy called LUTATHERA. It aims to evaluate the effectiveness and safety of a similar treatment called lutetium (177Lu) edotreotide or 177Lu-DOTATOC in patients who have these diseases but are outside the standard indications for LUTATHERA. The study focuses on expanding knowledge about this therapy's role in controlling disease and managing side effects. Participants receive treatment with 177Lu-DOTATOC given by slow intravenous infusion over 30 minutes using a pump system. The dose depends on patient risk factors: those with fewer than two risk factors receive 7.4 GBq per cycle, while those with two or more risk factors receive 5.5 GBq per cycle. Each participant will receive 4 cycles of treatment. Risk factors include kidney impairment, previous toxicities, uncontrolled diabetes or hypertension, prior therapies, and disease burden. During the study, participants will have regular assessments over several months, including scans to measure disease control at 32 months and ongoing monitoring up to 44 months for progression-free survival, overall survival, safety, and quality of life. Researchers will check blood tests, organ function, and side effects. This non-randomized phase 2 study allows patients with measurable or evaluable disease and progressive tumors confirmed by imaging to be included, with follow-up to evaluate response and safety.

Researchers are studying whether adjusting the dose of Lutetium-177 DOTATATE (Lutathera) based on individual dosimetry improves treatment results for adults with unresectable neuroendocrine tumors. This randomized controlled trial compares the standard fixed dose with a customized dosing approach guided by tumor and organ uptake, aiming to evaluate if personalized treatment can enhance outcomes. The study is sponsored by the University of Iowa and involves patients with well-differentiated gastroenteropancreatic neuroendocrine tumors. Participants will receive Lutathera through an intravenous infusion every 8 weeks for up to four cycles. The first dose is fixed at 200 millicuries for all participants. Those in the investigational group may receive higher doses (up to 400 millicuries) in subsequent cycles based on dosimetry imaging that tracks radiation exposure to tumors, kidneys, and bone marrow. The standard group continues with 200 millicuries per cycle. Imaging such as SPECT/CT scans and blood tests are performed to monitor the distribution and effects of the treatment. During the study, participants will undergo PET/CT scans before treatment, blood tests for several weeks after each Lutathera dose, and complete questionnaires about their health and symptoms. Follow-up visits occur about every 8 weeks during treatment and at 2, 3, 6, and 12 months after the last cycle. Long-term monitoring continues to assess side effects and treatment outcomes, including CT scans at 6 months and lifelong follow-up for radiation-related effects. The main outcome measure is the tumor response rate 6 months after treatment.

Researchers are evaluating the safety and effectiveness of a new molecular probe called 18F-FAPI-YQ104, which targets fibroblast activation protein (FAP), for early tumor diagnosis. This observational study focuses on patients with lung cancer, pancreatic cancer, neuroendocrine tumors, and thyroid cancer. The goal is to verify how well this probe works in detecting tumors during clinical use. Participants will receive an intravenous injection of the 18F-FAPI-YQ104 probe followed by a PET-CT examination to capture detailed images of tumor lesions. The study will observe the probe's uptake in tumor sites, measured by SUVmax values 60 minutes after administration. No additional treatment is given; instead, the study monitors the imaging results to assess the probe's diagnostic potential. During the study, participants will undergo PET-CT scans and other imaging tests such as CT or MRI. Researchers will evaluate the images to measure tumor activity and probe uptake. Safety assessments include checking kidney and liver function, blood counts, and monitoring for allergic reactions. The study will last from April 2025 to March 2026 and includes adults aged 18 to 75 years who have confirmed tumors and meet health criteria.

Researchers are evaluating the optimization of 18F-DOPA PET/CT imaging in specific patient groups including pediatric patients with congenital hyperinsulinism or neuroblastoma, pediatric and adult patients with neuroendocrine tumors or brain tumors, and adults suspected of Parkinson's disease or Lewy body dementia. The study aims to improve image quality using a new digital PET/CT scanner and intravenous furosemide, while also exploring gallbladder activity patterns related to dopaminergic degeneration. Participants will receive an intravenous injection of 18F-DOPA, with some also receiving a single intravenous dose of furosemide. The study includes a primary objective of assessing image quality improvements in the pelvis area and a secondary objective examining gallbladder activity patterns using dynamic imaging in a subgroup. Imaging data will be compared to previous scans with older technology. During the study, participants will undergo PET/CT scans, with measurements of lesion size and activity, bladder activity, and image artifact scoring. A questionnaire will screen for gallbladder disease history. The research team will analyze the imaging results and gallbladder activity patterns, with follow-up assessments occurring within one to three months. The total planned enrollment is 800 patients over approximately five years, with detailed monitoring of image optimization and gallbladder activity.

Researchers are evaluating the safety and sensitivity of a new imaging agent called 61Cu-NODAGA-LM3 compared to the standard 68Ga-DOTATOC for PET/CT scans in patients with well-differentiated bronchopulmonary and gastroenteropancreatic neuroendocrine tumors (NET). These tumors arise from neuroendocrine cells, often grow slowly, and may be metastatic at diagnosis. The study aims to improve diagnostic accuracy using this novel radiolabeled somatostatin receptor antagonist, which may offer advantages such as longer half-life and better tumor imaging contrast. Participants will receive a single intravenous dose of 61Cu-NODAGA-LM3 followed by up to three PET/CT scans. They will be randomly assigned to have the 61Cu-NODAGA-LM3 PET/CT either before or after their routine 68Ga-DOTATOC PET/CT, which is part of standard care. This open-label, randomized, controlled study takes place at one center and compares these two imaging approaches within a 24-hour to 4-week window. During the study, safety is monitored by tracking adverse events up to 18 hours after injection. Researchers will assess the sensitivity of 61Cu-NODAGA-LM3 imaging one hour after injection and evaluate various measures including tumor uptake, biodistribution, and patient preferences. Blood samples will be collected at multiple time points to study drug concentration and clearance. The total study duration spans from baseline assessments through imaging and follow-up, helping to understand the potential of 61Cu-NODAGA-LM3 in managing neuroendocrine tumors.

Researchers are evaluating the safety profile of the PET radiotracer 68Ga-DOTA-TATE to support its use as a routine standard-of-care diagnostic tool for patients with neuroendocrine tumors (NET). This pragmatic clinical trial is prospective, non-randomized, and open-label, conducted at a single center with recruitment across Canada. Previous studies have shown that 68Ga-DOTA-TATE is superior to the former standard-of-care imaging method, Octreoscan, and this trial aims to collect further data to support its adoption for NET patients. Participants referred by their physicians who meet eligibility criteria will receive an intravenous injection of 68Ga-DOTA-TATE at a dose of 3 MBq/kg, up to a maximum of 370 MBq. After waiting 45 to 90 minutes, patients will undergo imaging using a PET/CT scanner. The images will be reviewed by trained nuclear medicine physicians. The study will monitor the safety profile of the radiotracer, including any adverse effects, false positives or negatives, and abnormal biodistribution. During the study, participants will be assessed for safety outcomes over five years, including monitoring for any side effects and the clinical impact of imaging on patient management. Data collected will help establish 68Ga-DOTA-TATE as a routine diagnostic tool for NET. The study will track safety and clinical outcomes to support this implementation while ensuring ongoing observation and care for participants throughout the study period.

Researchers are evaluating the safety and diagnostic accuracy of 68Ga-HA-DOTATATE PET/CT imaging for patients with known or suspected somatostatin receptor positive tumors, such as gastrointestinal, pancreatic, pulmonary neuroendocrine tumors, and others. This phase II, single-center, non-randomized study aims to assess this new tracer produced at the Edmonton Radiopharmaceutical Centre, comparing it to standard CT or MRI imaging over a one-year follow-up period. Participants will receive a single intravenous dose of 68Ga-HA-DOTATATE at 2.64 MBq/kg, with a minimum of 37 MBq and maximum of 250 MBq, followed by PET/CT scanning. Up to 600 scans will be performed over six years, including both adult and pediatric patients. Some patients may undergo multiple scans during the study. Safety will be monitored immediately after injection, post-scan, and at 10 days, while efficacy will be evaluated by comparing imaging results to clinical follow-up. During the study, participants will undergo PET/CT scans and standard clinical CT or MRI within six months before enrollment. Adverse events will be tracked closely in the Nuclear Medicine department, and diagnostic accuracy will be assessed through sensitivity and specificity measures at one year post-scan. The study duration allows for comprehensive safety and efficacy evaluations, helping to inform clinical care for patients with these tumors.

This research aims to evaluate a new drug called ADCT-701 in adults with neuroendocrine neoplasms (NENs), including rare cancers found in the gastrointestinal tract, pancreas, lungs, adrenal glands, and other areas. These cancers often have a high risk of returning and low survival rates, and current treatments have limited benefits. The study is a first-in-human Phase I trial designed to find the maximum tolerated dose of ADCT-701, a drug targeting DLK1, which is present in various neuroendocrine tumors and related cancers. Participants will receive ADCT-701 as an intravenous infusion over 30 to 45 minutes on the first day of each 21-day treatment cycle. The study uses a dose-escalation design to determine the best dose, with up to 10 dose levels tested in approximately 70 patients. Treatment can continue for up to two years. After completing treatment, participants will have follow-up visits including physical exams, heart and blood tests, and imaging scans for up to five years to monitor health and disease status. During the study, participants will undergo screening that includes physical exams, blood and urine tests, imaging scans, heart function tests, and possibly a tumor biopsy. Clinic visits are frequent at first, with 10 visits over the first two cycles, then two visits per cycle thereafter. Each visit may last up to eight hours and includes repeated tests and assessments of daily activity ability. Researchers will monitor safety, drug levels in the body, immune responses, and antitumor activity throughout the trial and follow-up periods.

Researchers are evaluating a new rehabilitation process to assess and relieve chemotherapy-induced peripheral neuropathy in the feet of patients treated for early-stage breast cancer. This study compares two orthopedic supports: a standard treatment using customized insoles and shoes, and a novel silicone orthosis designed as a soft, sock-like device for indoor use. The goal is to understand if the silicone orthosis can reduce symptoms and improve function compared to standard treatment. Participants will be randomly assigned to receive either the customized insoles and shoes or the silicone orthosis along with the standard treatment. The study involves initial assessments including symptom grading, foot health questionnaires, quality of life scales, and 3D foot scanning. Activity levels will be tracked using an activity sensor worn on the leg for two weeks. Participants using the silicone orthosis will keep a diary of device usage. Follow-ups occur 3 to 6 weeks after starting the intervention to evaluate symptom changes and patient experiences. During the study, participants will undergo foot examinations and complete questionnaires about their symptoms, foot health, and quality of life. Mobility and activity patterns will be monitored objectively with activity trackers. Follow-up may be conducted in person, by phone, or digitally, lasting about 45 minutes. The main outcomes include changes in neuropathy symptoms and physical activity after 3 to 6 weeks of using the orthopedic devices. This research aims to improve rehabilitation care for breast cancer survivors experiencing foot neuropathy from chemotherapy.

Researchers are studying CHM-2101, an autologous CDH17 CAR T-cell therapy, in a Phase 1/2 open-label trial for patients with advanced gastrointestinal cancers that have returned or not responded to at least one standard treatment in metastatic or locally advanced stages. The study aims to evaluate the safety and effects of this therapy in treating gastric adenocarcinoma, colorectal cancer, and certain neuroendocrine tumors. It is sponsored by Chimeric Therapeutics and focuses on patients who have undergone prior treatments. The trial includes two parts: Phase 1 with dose escalation and expansion, and Phase 2. Participants first provide consent and undergo screening before leukapheresis, a procedure to collect immune cells for manufacturing the CHM-2101 therapy. After cell collection, participants may receive bridging chemotherapy to maintain disease stability if needed. Treatment involves three daily intravenous doses of fludarabine and cyclophosphamide followed by a single intravenous infusion of CHM-2101. The dose in Phase 1 follows a "3+3" escalation design to determine the recommended dose for Phase 2. Participants will be monitored for up to 18 months or until their disease progresses. Assessments include safety evaluations focusing on dose-limiting toxicities, cytokine release syndrome, adverse events, and objective tumor response. Secondary outcomes include disease control, response duration, and survival measures. Laboratory tests, imaging, and clinical evaluations will be used to follow participants' health and treatment effects throughout the study.