Clinical Trials Logo

Clinical Trial Summary

Many patients with cancer have insufficient vitamin D levels, and low vitamin D levels are associated with increased 'all-cause mortality' and especially mortality due to cancer. Vitamin D has anti-cancer effects, including anti-proliferation, anti-angiogenesis, and anti-inflammation. Besides, low vitamin D levels are associated with higher opioid dose usage, fatigue, and impaired quality of life in palliative cancer patients. Therefore, patients with low vitamin D levels needs instant vitamin D supplement with "stoss therapy" which is single high dose vitamin D with maintenance dose by enteral route. The stoss therapy has been applied in many fields, including neonatal, diabetes, hemodialysis, heart failure, osteoporosis. In critically ill patients, such as surgical, medical, burn intensive unit admission patients, high dose vitamin D supplement was associated lower mortality amount the vitamin D deficiency patients. This study aims for evaluating the effects of enteral high dose vitamin D supplement on advanced cancer patients with pain, serum concentration changes of vitamin D, quality of life, symptom burden, and analyze its correlation with inflammation, immune and nutritional markers.


Clinical Trial Description

In recent years, it has become evident that vitamin D is important for several different functions in the body including the immune system, nervous system and the cardiovascular system. Vitamin D affects the human immune system in several ways, including induction of antimicrobial peptides (AMPs), which are not only important for the defense against bacteria but might also be important for killing malignant cells. Several observational studies show that patients with cancer generally have lower vitamin D levels than healthy controls. There is a consensus that very low serum levels of 25OHD (<25 nmol/L) reflect a true vitamin D deficiency and consider levels below 50 nmol/L to represent vitamin D insufficiency. In a meta-analysis of 159 randomized controlled trials, it was shown that treatment with vitamin D3 was associated with decreased all-cause mortality and especially that mortality caused by cancer was significantly reduced (RR 0.88 (95% confidence interval 0.78 to 0.98); p=0.02; n=44.492). A Sweden observational study of 100 cancer patients with palliative care showed that low 25OHD levels are associated with increased pain and higher opioid dose, higher infectious burden, and impaired quality of life. A cross-sectional study showed positive correlation of vitamin D status with absence of fatigue and improved physical and functional well-being in 30 advanced cancer patients receiving palliative care. A Sweden matched case-control study demonstrated, in 39 palliative cancer patients, vitamin D supplement (4000 IU/day) significantly decreased fentanyl dose compared to the untreated group. The vitamin D treated group had improved quality of life and lower consumption of antibiotics. Besides, vitamin D was well tolerated by all patients. A recent phase II SUNSHINE trial compared addition of high-dose (vitamin D3 po 8,000 IU/d x 2 weeks as loading dose followed by 4,000 IU/d) and standard-dose (standard vitamin D3 400 IU/d) vitamin D supplement to chemotherapy in patients with metastatic colorectal cancer, which demonstrated the high-dose group resulted in a difference in median progression free survival that was not statistically significant, but with a significantly improved supportive hazard ratio. A dosing strategy can be utilized for the treatment of vitamin D deficiency, known as "stoss therapy", which has been utilized for a long time. For patients over 1 month of age, 100,000 to 600,000 units of vitamin D can be given orally as a single dose, followed by maintenance doses. The stoss therapy has been used to prevent and treat infant and childhood vitamin D deficiency since 1930s. In the recent years, vitamin D stoss therapy has given to patients in the intensive care unit. Quraishi team conducted a randomized control trial which compared placebo (n = 10) versus single dose of enteral 200,000 IU vitamin D (n = 10) versus 400,000 IU vitamin D (n = 10), within 24 hours of new-onset severe sepsis or septic shock. Compared with placebo, the higher dose group had fewer hospital length of stay. A pilot double blind randomized control trial conducted on mechanically ventilated adult ICU patients. A total 30 patients were administered either placebo, 50,000 IU vitamin D3 or 100,000 IU vitamin D3 daily for 5 consecutive days enterally. Higher dose vitamin D3 safely increased plasma 25(OH)D concentrations into the sufficient range and was associated with decreased hospital length of stay. Currently, there are several ongoing clinical trial regarding the use of high dose vitamin D in patients admitted in the intensive care unit. A clinical trial has been conducted at National Taiwan University Hospital, in which a total of 569,600 IU of enteral vitamin D3 or placebo is administered in one week for patients in intensive care units (ClinicalTrials.gov NCT02594579). Another study is conducted in Tri-service Hospital aimed to test the effects of high dose vitamin D3 (1.29 million IU vitamin D3 administered within one month) in patients with esophageal cancer undergoing operation. A randomized double-blind control trial is conducted in Thailand to test the effect of vitamin D3 supplementation on muscle mass in ICU patients, in which vitamin D3 100,000 IU/day on day 1,3, then 50,000 IU/day on day 5,7,9,12 and 50,000 IU 3 times/week for 4 weeks (ClinicalTrials.gov NCT02594579). This study will be conducted as a randomized control trial to determine the effects of high dose vitamin D on advanced cancer patients' pain, increase of 25(OH)D levels to at least 30 ng/mL, quality of life, symptom burden, and analyze its correlation with inflammation, immune and nutritional markers. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05450419
Study type Interventional
Source Chang Gung Memorial Hospital
Contact Li-Ting Lian
Phone +886-224329292
Email liting@cgmh.org.tw
Status Recruiting
Phase N/A
Start date July 1, 2021
Completion date June 30, 2025

See also
  Status Clinical Trial Phase
Completed NCT03181854 - Randomized Controlled Trial of Integrated Early Palliative Care N/A
Completed NCT01197170 - Hormone Receptor Positive Disease Across Solid Tumor Types: A Phase I Study of Single-Agent Hormone Blockade and Combination Approaches With Targeted Agents to Provide Synergy and Overcome Resistance Phase 1
Recruiting NCT05045040 - Empathetic Communication Facilitation Program for Early Initiation of End-of-life Discussions N/A
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
Active, not recruiting NCT03994601 - An Investigational Immunotherapy Study of BMS-986288 Alone and in Combination With Nivolumab in Advanced Solid Cancers Phase 1/Phase 2
Active, not recruiting NCT03667716 - COM701 (an Inhibitor of PVRIG) in Subjects With Advanced Solid Tumors. Phase 1
Completed NCT01393990 - A Study of LY2228820 in Participants With Advanced Cancer Phase 1
Completed NCT02857270 - A Study of LY3214996 Administered Alone or in Combination With Other Agents in Participants With Advanced/Metastatic Cancer Phase 1
Recruiting NCT03175224 - APL-101 Study of Subjects With NSCLC With c-Met EXON 14 Skip Mutations and c-Met Dysregulation Advanced Solid Tumors Phase 2
Active, not recruiting NCT04121676 - Anti-CD137 and Anti-CTLA-4 Monoclonal Antibody in Patients With Advanced Cancer Phase 1
Active, not recruiting NCT03177291 - Pirfenidone Combined With Standard First-Line Chemotherapy in Advanced-Stage Lung NSCLC Phase 1
Completed NCT03980041 - Study to Evaluate the Efficacy/Safety of IPI-549 in Combination With Nivolumab in Patients With Advanced Urothelial Carcinoma (MARIO-275) Phase 2
Active, not recruiting NCT03674567 - Dose Escalation and Expansion Study of FLX475 Monotherapy and in Combination With Pembrolizumab Phase 1/Phase 2
Recruiting NCT04823377 - Impact of a Process Optimizing the Decision to Continue or Stop Cancer Treatments in Patients With Advanced Non-small Cell Lung Cancer. N/A
Completed NCT02778126 - A Study of Prexasertib (LY2606368) in Participants With Advanced Cancer Phase 1
Completed NCT02507544 - A Safety and Pharmacokinetic Study of TRX-818 Administered Orally to Patients With Advanced Cancer Phase 1
Completed NCT02529553 - A Study of LY3076226 in Participants With Advanced or Metastatic Cancer Phase 1
Completed NCT02245204 - Phase I Studies of Chlorogenic Acid for Injection for Tolerance and Pharmacokinetic of Advanced Cancers Phase 1
Completed NCT01583777 - Phase I Mass Balance, PK and Safety Study of 14C-Labeled Belinostat in Patients With Advanced Cancer Phase 1
Completed NCT01901237 - Yoga for Adolescent and Young Adult Non-Curative Cancer Patients N/A