Rapamycin (Sirolimus) (partial)
Also known by these names
Rapamycin is a soil-derived antibiotic that binds to a target protein enzyme (mTOR) that controls cell growth, proliferation and survival. By blocking certain functions of the mTOR enzyme, rapamycin reduces cell growth. It therefore may be useful in treating or preventing proliferative diseases, including cancer.
Rapamycin received US FDA approval in 2003 for use in preventing acute rejection in kidney transplantation.1
Treating the Cancer
Working against cancer growth or spread, improving survival, or working with other treatments or therapies to improve their anticancer action
Everolimus and Rapamycin
The conventional cancer treatment everolimus (Medline Plus) is a later generation of rapamycin (sirolimus). Along with temsirolimus, everolimus is a derivative of sirolimus approved for treating renal cell carcinoma. A number of clinical studies have investigated the use of everolimus in cancers including breast and colorectal.
European Medicines Agency (EMA) has approved everolimus (Afinitor®) for the treatment of hormone receptor-positive, HER2/neu-negative advanced breast cancer,2 and the US Food and Drug Administration approved use in treatment of postmenopausal women with advanced hormone receptor-positive, HER-2 negative breast cancer in combination with exemestane, after failure of treatment with letrozole or anastrozole.3
Compared to everolimus, rapamycin is not only less expensive, but it may be less toxic. Integrative oncologist and BCCT advisor Dwight McKee, MD, considers using rapamycin with patients who demonstrate upregulated mTOR. See his Commentary below.
In many cancers, an intracellular signaling pathway important in regulating the cell cycle (the PI3K-AKT pathway) is overactive. This overactive pathway reduces normal cell death (apoptosis) and allows cells to grow abnormally. Rapamycin can inhibit cells that express the active form of AKT,4 and is therefore being investigated as a cancer treatment or adjuvant (supplemental) therapy.
- High response and cancer control rates when rapamycin and hydroxychloroquine were added to metronomic chemotherapy (also called low-dose chemotherapy) for refractory metastatic solid tumors (bladder, breast, colon, head and neck, lung and prostate) in a small group of patients who didn't respond to first-line metronomic chemotherapy5
- Tolerated by most patients when used with the chemotherapy drug bevacizumab, at lower cost than other mTOR inhibitors, but without significant treatment effects in patients with pathologically confirmed advanced solid tumors for which standard curative or palliative measures either do not exist or were no longer effective6
Lab and Animal Evidence
- Enhanced response to erlotinib (used to treat certain types of non-small cell lung cancer), inhibiting cell growth pathways in cell and animal models7
- Variable response rates for different tumor types, from melanoma zero percent to ovarian 41 percent8
- Increased anticancer effect when used with herceptin (a drug used to treat HER2-positive cancers including HER2-positive breast cancer) compared to either drug alone in breast cancer cells overexpressing HER2-neu (a protein involved in cell growth)9
- Stopped growth in breast carcinoma cells in cell studies and reduced growth of breast cancer cells grafted into animals, when given with cotylenin A10
Head and Neck Cancer
- Antitumor activity in animal models of head and neck squamous cell carcinoma comparable to the more expensive derivative temsirolimus11
- Enhanced effects of cancer treatments gefitinib and erlotinib (EGF receptor inhibitors) in suppressing cell growth12
- Enhanced effects of EGF receptor inhibitors against non-small-cell lung cancer cells13
- Reduced epidermal growth factor-induced HCCR expression in pancreatic cancer cells; HCCR expression plays a key role in pancreatic tumor progression14
Optimizing Your Terrain
Creating an environment within your body that does not support cancer development, growth or spread
A high rate of grade 3 (severe and undesirable adverse event) postoperative toxicity has been found when used too soon after surgery; researchers recommended waiting six weeks after surgery before use.16
BCCT does not recommend therapies or doses, but only provides information for patients and providers to consider as part of a complete treatment plan. Patients should discuss therapies with their physicians, as contraindications, interactions and side effects must be evaluated.
Dosage information and recommendations are available from these sources:
Integrative Programs, Protocols and Medical Systems
|For more information about programs and protocols, see our Integrative Programs and Protocols page.|
Rapamycin is not yet listed in any of the protocols or systems that BCCT references. However, see Dwight McKee’s comments below.
From integrative oncologist and BCCT advisor Dwight McKee, MD, April 23, 2020: Rapamycin is not FDA-approved for any cancer indications, so its use would still be considered off-label use in cancer. I prefer it to everolimus and temsirolimus because of its much lower toxicity. Because of its very long half life, it can be dosed weekly. I have usually recommended 5-8 mg, depending on body size. It's very useful to combine resveratrol and/or its cousin pterostilbene (500 mg bid for resveratrol, 250 mg bid for peterostilbene), as they effectively block the downstream signalling pathways of mTOR (PI3K and PTEN).
I would recommend weekly rapamycin and resveratrol/pterostilbene for cancers in which mTOR is upregulated, as indicated by genomics, RNA expression, and/or proteomics. It's ALWAYS a good idea to get genomic, RNA and/or proteomic testing, as mTOR upregulation is not predictable. It’s also good to look at downstream PI3K and PTEN when determining who might benefit from rapamycin, though most oncologists tend to go with mTOR if it's upregulated. I don't go by which cancers everolimus is indicated for. A person’s mTOR status is much more specific.
Taking 3 to 4 mg of rapamycin (sirolimus) with 8 ounces of grapefruit juice can save money. In this dose range there are typically no side effects noted. A phase 1 trial which studied the effect of grapefruit juice as well as a drug (ketoconazole) on slowing the metabolism of sirolimus used much higher doses of sirolimus, which did produce some side effects, and also might be associated with some immune suppression.17 3-4 mg taken with grapefruit juice weekly (or 6-8 mg without grapefruit juice) is adequate to suppress m-TOR signaling and allow other components of a comprehensive integrative approach to cancer treatment to work better, with no perceivable side effects or immunosuppression.
Non-cancer Uses of Rapamycin
BCCT has not reviewed the effectiveness of this therapy for non-cancer uses.
Written by Laura Pole, RN, MSN, OCNS, and Nancy Hepp, MS, and reviewed by Maria Williams; last update November 23, 2020.
- Cancer Strategies Journal: 2013 Summer Clinical Pearls