Case Reports in Pancreatic Cancer, Volume 2.1, 2016, DOI: 10.1089/crpc.2016.0003
- A woman with pancreatic cancer decided from the internet to take 50,000 IU of vitamin D daily
- She got her Vitamin D level to >150 ng
- 10 months later, without radiation therapy and with only one dose of Chemo she was well and without symptoms
- The researchers refered to her condition as "stabillized", but it seems more than stabilized, since her health improved
- The researchers were considering a trial for % "cured" with extremly high doses of vitamin D
- No clinical trials listed for Pancreatic Cancer with >4,000 IU of Vitamin D as of June 2018, 2 years after publication of the study
- Note The MS Vitamin D dosing (see below) needed to get to individuals to 150 ng ranged from 20,000 to 140,000 IU daily
- Cancer - Pancreatic category listing has
56 items along with related searches
- Vitamin D 100,000 IU daily was OK for Dr. Cannell for 6 months – Jan 2015 Dr. Cannell
- 50000 IU vitamin D daily toxic after 3 months – Oct 2011
However, balancing the co-factors avoids long-term Vitamin D toxicity
- Over 2,000 people have been cured of Multiple Sclerosis after a protocol which includes > 150 ng of vitamin D
Addition of Omega-3 would probably augment high dose Vitamin D
- Severe acute pancreatitis treated in 11 ways by Omega-3 in just 7 days – RCT April 2018
- Google query Pancreatic Cancer" ("vitamin d" AND omega-3) ==> 380.000 hits June 2018
Timothy L. Cannon,1'* Joel Ford,2 Danubia Hester,2 and Donald L. Trump1
1 Inova Schar Cancer Institute, Fairfax, Virginia.
2 Inova Medical Center, Falls Church, Virginia.
* Inova Schar Cancer Institute, 8505 Arlington Blvd., Suite 100, Fairfax, VA 22031, E-mail: timomothy.cannon at gmail.com
Background: Pancreatic adenocarcinoma is associated with a very poor prognosis, with a 5 year survival of 7.2%. Vitamin D has long been evaluated for benefit as a protective agent and treatment for malignancies. Although cancer incidence and outcomes have been tied to vitamin D levels, there is no clear evidence that supplementation of vitamin D improves outcome in pancreatic cancer to date.
Case Presentation: We present a patient who errantly took supratherapeutic doses of vitamin D 50,000 U daily, achieving a serum 25(OH)D level of more than 150ng/mL, with no appreciable side effects.
Conclusion: Her disease was stable for 8 months off of this was related to vitamin D supplementation.
Pancreatic cancer is the third most common cause of cancer death in the United States, with more than 40,000 deaths per year.1 The 5 year survival for all stages of pancreatic adenocarcinoma is * 7.2%.2,3 Reasons for poor outcomes include the advanced state at diagnosis, a location that makes resection difficult, and poor sensitivity to chemotherapy. For this reason, novel approaches are needed to improve outcomes.
Vitamin D has long been evaluated for benefit as a protective agent and treatment for malignancies.4,5 Giovannucci et al. demonstrated a statistically significant difference in cancer incidence between those in the bottom decile of predicted 25(OH)D levels and those in the top decile.6 Outcomes in colorectal cancer are more favorable for those with higher levels of 25(OH)D.7 Although correlation data have been promising, treatment with vitamin D has shown inconsistent results. Increased intake appears to decrease the risk of colon cancer,8-10 but has not shown to improve outcomes in other malignancies.11-13
Vitamin D impacts cancer cell growth and differentiation.14,15 In pancreatic cancer preclinical models, conventional treatment, although it is unclear whether the administration of 1,25(OH)2D analogues causes apoptosis, has antiproliferative effects, and inhibits angiogenesis.16-18 The vitamin D receptor (VDR) is involved in multiple metabolic pathways, most notably mineral metabolism, the immune response, and malignancy.19-22 The receptor is the mediator of the physiological actions of active forms of vitamin D. Activation of VDR antagonizes the activity of TGFBeta, a promoter of fibrogenesis, correcting maladaptive proin-flammatory responses that stimulate oncogenesis.23-26
VDRs are ubiquitous within stellate cells in the stroma of pancreatic ductal adenocarcinoma.27 Albrechtsson et al. found a more than threefold increase in human cancer cell lines than the normal pancreas.28 The stroma, consisting of fibroblastic cells, immune cells, blood vessels, and matricellular proteins, plays a crucial role in promoting and sustaining tumor growth.29,30 These tasks are carried out through paracrine stimulation.31 In addition, the stroma facilitates resistance to chemotherapy by forming a physical blockade to penetration. In their active state, stellate cells are proinflammatory. However, in a quiescent state, they are producing extracellular matrix at low levels.32,33 In murine models,
Patient A.N. is an 83-year-old woman who was living in Iran in January of 2015 when she presented to a local hospital with painless jaundice and dark urine. A CT scan showed a pancreatic head mass compressing the common bile duct. For palliation of hyperbilirubinemia, a palliative stent was placed in the common bile duct. A fine needle aspirate obtained through an endoscopic ultrasound (EUS) revealed a poorly differentiated adenocarcinoma. A follow-up CT scan performed on February 13, 2015 revealed a 3.6 X 2.7 cm pancreatic head mass that abutted the superior mesenteric artery and one of its proximal branches. There were suspicious peripancreatic and retroperitoneal nodes and no evidence of distant disease. At the beginning of March, she began taking 50,000 U vitamin D3 (cholecalciferol) daily, ordered directly from the Internet and not under the direction of a healthcare practitioner. Repeat EUS and biopsy on March 3, 2015 again confirmed adenocarcinoma with papillary features. She was referred to an oncologist and surgeon for evaluation. A triple phase CT was done on March 16, 2015 that showed a stable mass without any evidence of involvement of the celiac axis or superior mesenteric artery. Upfront chemotherapy was recommended, with consideration of surgery in the future.
She received gemcitabine/protein nanoparticle-bound paclitaxel in March. On day 10 of cycle 1, she developed neutropenic fever complicated by atrial fibrillation with rapid ventricular response. She was intubated for a brief time who then recovered to her baseline functional status. She was discharged on April 19. Based on her frailty, she was deemed to be a poor candidate for surgery and chemotherapy was not resumed.
She was referred to radiation oncology for consideration of stereotactic body radiotherapy, but she decided to first pursue alternative therapies.
She visited an alternative care clinic in April and began taking chelodium, curcumin, community mushroom blend, viscosin, and naltrexone.
She also continued to take her daily dose of 50,000 U vitamin D3. Although she was somewhat inconsistent in taking her regimen prescribed by the alternative therapy clinic, she consistently took the same vitamin D3 dose from April until the time of writing.
She was seen first at the Inova Schar Cancer Institute in September 2015. On September 4, 2015, CT scan revealed the pancreatic head mass to be 3.1 X 3.0 cm, slightly smaller than previously with a mild increase in pancreatic duct dilatation. On our first visit on September 5, 2015, we did not obtain a full supplement history, but checked a vitamin D, 25 OH level, which surprisingly was elevated above normal value of >150ng/mL. Her calcium level was 9.7, which had been 7.7 in March 2015, before starting supplementation. In October, 8 months after her only dose of chemotherapy, she had a CT scan that showed continued disease stability (Fig. 1). As of December 4, 2015, she was stable with no evidence of disease progression by both CT and CA 19-9 level. She was admitted to Fairfax hospital in October of 2015 for diverticulitis with abscess formation that was treated with resection. Currently she describes as feeling quite well with no difficulty accomplishing her activities of daily living.
Several clinical trials are underway that are investigating the use of ˜high-dose” vitamin D. To our knowledge, no trial is investigating a supplement dose that approaches the level taken by the subject of this case report.35,36 For example, NCT01150877, a trial designed to aggressively raise the serum 25(OH)D levels of colorectal cancer patients, aims for a serum (OH)D level of 80-100 ng/mL.35 The dose taken by patient A.N. achieved a serum (OH)D level of >150 ng/mL. This dose, initiated through a misunderstanding of the appropriate dose, was very well tolerated with no apparent side effects.
In the phase III MPACT study, the gemcitabine/ protein-bound nanoparticle paclitaxel arm had a median progression-free survival (PFS) of 5.5 months.37 Patient A.N. had an 8 month PFS despite not even completing one cycle of combination chemotherapy. One cannot conclude that her vitamin D dose was in any way related to this outcome. There is only one CT scan before the initiation of vitamin D, and there is no way to know what her pace of disease would have been in the absence of vitamin D supplementation. In addition, she was taking several other supplements such as shitake mushrooms, although inconsistently and for a shorter duration, which were also intended to treat her malignancy.
Nonetheless, given the poor prognosis of pancreatic cancer and the limited treatment options for patients, this case should stimulate further investigation. The daily dose of 50,000 U of vitamin D3 was well tolerated in our patient for over 10 months at the time of writing. Consideration should be given to a clinical trial that evaluates a similar dose. Correlatives may include an evaluation of gene expression changes as well as phenotypical changes in the stroma.
- Although epidemiological data have been suggestive of a correlation between vitamin D levels and cancer incidence, there is no evidence of a positive impact of vitamin D supplementation on pancreatic cancer outcome.
- Vitamin D impacts the stroma in murine models of pancreatic cancer, resulting in a more quiescent phenotype.
- The patient in the case report tolerated a dose of 50,000 U of vitamin D3 over an 10 month period.
- Vitamin D at high doses should be investigated as a novel therapeutic agent for pancreatic adenocarcinoma.
Pancreatic Cancer stabilized by a woman taking 50,000 IU of vitamin D daily - 2016
- 1. Seer.cancer.gov. Cancer of the Pancreasâ€”SEER Stat Fact Sheets. 2015. Available from: http://seer.cancer.gov/statfacts/html/pancreas.html (accessed December 17, 2015).
- 2. Cancer.org. Pancreatic cancer survival by stage. 2015. Available from: www.cancer.org/cancer/pancreaticcancer/detailedguide/pancreatic-cancer-survival-rates (accessed December 17, 2015).
- 3. Boeck S, Ankerst D, Heinemann V. The role of adjuvant chemotherapy for patients with resected pancreatic cancer: systematic review of randomized controlled trials and meta-analysis. Oncology. 2007;72:314-321.
- 4. Peller S, Stephenson C. Skin irritation and cancer in the U.S. Navy. Am J Med Sci. 1937;194:326-333.
- 5. Apperly F. The relation of solar radiation to cancer mortality in northern America. J Cancer Res. 1941;1:191-195.
- 6. Giovannucci E, Liu Y, Rimm E, et al. Prospective study of predictors of vitamin D status and cancer incidence and mortality in men. J Natl Cancer Inst. 2006;98:451-459.
- 7. Ng K. Vitamin D status and survival of metastatic colorectal cancer patients: results from CALGB/SWOG 80405 (Alliance). 2015 Gastrointestinal Cancers Symposium. J Clin Oncol 2015;13. Available from: http://meetinglibrary.asco.org/content/139861-158 (accessed December 17, 2015).
- 8. Garland C, Barrett-Connor E, Rossof A, et al. Dietary vitamin D and calcium and risk of colorectal cancer: a 19-year prospective study in men. Lancet. 1985;325:307-309.
- 9. Lappe J, Travers-Gustafson D, Davies K, et al. Vitamin D and calcium supplementation reduces cancer risk: results of a randomized trial. Am J Clin Nutr. 2007;85:1586-1591.
- 10. Ma Y, Zhang P, Wang F, et al. Association between vitamin D and risk of colorectal cancer: a systematic review of prospective studies. J Clin Oncol. 2011;29:3775-3782.
- 11. Purdue M, Freedman D, Gapstur S, et al. Circulating 25-hydroxyvitamin D and risk of non-Hodgkin Lymphoma: cohort consortium vitamin D pooling project of rarer cancers. Am J Epidemiol. 2010;172:58-69.
- 12. Weinstein S, Purdue M, Smith-Warner S, et al. Serum 25-hydroxyvitamin D, vitamin D binding protein and risk of colorectal cancer in the prostate, lung, colorectal and ovarian cancer screening trial. Int J Cancer. 2014;136: E654-E664.
- 13. Van Loon K, Owzar K, Jiang C, et al. 25-Hydroxyvitamin D levels and survival in advanced pancreatic cancer: findings from CALGB 80303 (Alliance). J Natl Cancer Inst. 2014;106:dju185.
- 14. Colston K. Mechanisms implicated in the growth regulatory effects of vitamin D in breast cancer. Endocr Relat Cancer. 2002;9:45-59.
- 15. Palmer H. Vitamin D3 promotes the differentiation of colon carcinoma cells by the induction of E-cadherin and the inhibition of beta-catenin signaling. J Cell Bio. 2001;154:369-388.
- 16. Colston K, James S, Ofori-Kuragu E, et al. Vitamin D receptors and antiproliferative effects of vitamin D derivatives in human pancreatic carcinoma cells in vivo and in vitro. Br J Cancer. 1997;76:1017-1020.
- 17. Zugmaier G, Jager R, Grage B, et al. Growth-inhibitory effects of vitamin D analogues and retinoids on human pancreatic cancer cells. Br J Cancer. 1996;73:1341-1346.
- 18. Deeb K, Trump D, Johnson C. Vitamin D signalling pathways in cancer: potential for anticancer therapeutics. Nat Rev Cancer. 2007;7:684-700.
- 19. Quarles L. Skeletal secretion of FGF-23 regulates phosphate and vitamin D metabolism. Nat Rev Endocrinol. 2012;8:276-286.
- 20. Hahn T. 6 Drug-induced disorders of vitamin D and mineral metabolism. Clin Endocrinol and Metab. 1980;9:107-129.
- 21. Gutierrez O, Farwell W, Kermah D, et al. Racial differences in the relationship between vitamin D, bone mineral density, and parathyroid hormone in the National Health and Nutrition Examination Survey. Osteoporosis Intl. 2010;22:1745-1753.
- 22. Bhan I, Powe C, Berg A, et al. Bioavailable vitamin D is more tightly linked to mineral metabolism than total vitamin D in incident hemodialysis patients. Kidney Int. 2012;82:84-89.
- 23. Zhang Y, Guo Q, Zhang Z, et al. VDR status arbitrates the prometastatic effects of tumor-associated macrophages. Mol Cancer Res. 2014;12: 1181-1191.
- 24. Ding C, Gao D, Wilding J, et al. Vitamin D signaling in adipose tissue. Br J Nutr. 2012;108:1915-1923.
- 25. Skinner H. Vitamin D intake and the risk for pancreatic cancer in two cohort studies. Cancer Epidemiol Biomarkers Prev. 2006;15:1688-1695.
- 26. Wolpin B, Ng K, Bao Y, et al. Plasma 25-hydroxyvitamin D and risk of pancreatic cancer. Cancer Epidemiol Biomarkers Prev. 2011;21:82-91.
- 27. Sherman M, Yu R, Engle D, et al. Vitamin D receptor-mediated stromal reprogramming suppresses pancreatitis and enhances pancreatic cancer therapy. Cell. 2014;159:80-93.
- 28. Albrechtsson E, Jonsson T, Moller S, et al. Vitamin D receptor is expressed in pancreatic cancer cells and a vitamin D3 analogue decreases cell number. Pancreatology. 2003;3:41-46.
- 29. Neesse A, Algul H, Tuveson D, et al. Stromal biology and therapy in pancreatic cancer: a changing paradigm. Gut. 2015;64:1476-1484.
- 30. Neesse A, Michl P, Frese K, et al. Stromal biology and therapy in pancreatic cancer. Gut. 2010;60:861-868.
- 31. Hwang R, Moore T, Arumugam T, et al. Cancer-associated stromal fibroblasts promote pancreatic tumor progression. Cancer Res. 2008;68:918-926.
- 32. Abramovitch S, Dahan-Bachar L, Sharvit E, et al. Vitamin D inhibits proliferation and profibrotic marker expression in hepatic stellate cells and decreases thioacetamide-induced liver fibrosis in rats. Gut. 2011;60:1728-1737.
- 33. Ding N, Yu R, Subramaniam N, et al. A Vitamin D receptor/SMAD genomic circuit gates hepatic fibrotic response. Cell. 2013;153:601-613.
- 34. American Association for Cancer Research. Genetic marker in vitamin D receptor gene associated with increased pancreatic cancer survival. ScienceDaily. 2012. Available from: www.sciencedaily.com/releases/2012/06/120619225733.htm (accessed December 17, 2015).
- 35. University of British Columbia. Study of high-dose vitamin D supplementation in stage-4 colorectal cancer patients. ClinicalTrials.gov 2015. Available from: https://clinicaltrials.gov/ct2/show/NCT01150877 (accessed December 17, 2015).
- 36. Dana Farber Cancer Center. Study of vitamin D in untreated metastatic colorectal cancer. ClinicalTrials.gov 2015. Available from: https://clinical-trials.gov/ct2/show/NCT01516216 (accessed December 17, 2015).
- 37. Van Hoff DD, Ervin T, Arena FP, et al. Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine. N Engl J Med. 2013;369: 1691-1703.
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