palbociclib
Trade Name:Ibrance™
Appearance:Tablet or capsule in various strengths and colours
Monograph Name:palbociclib
Monograph Body:
Palbociclib is a selective, reversible small molecule inhibitor of cyclin-dependent kinases (CDK) 4 and 6. The drug inhibits cyclin D-CDK 4/6 complex activity, blocking cell cycle progression from G1 to S phase. Palbociclib in combination with an anti-estrogen agent inhibits cell proliferation and induction of cell senescence in estrogen receptor (ER) positive breast cancer models.
Bioavailability |
46% (mean) |
Peak plasma levels |
6 to 12 hours (capsule); 4 to 12 hours (tablet) |
Time to reach steady state |
8 days |
Effects with food |
Capsule: When administered with food, AUC and Cmax increased (up to 21% and 38%, respectively) and exposure variability decreased. Palbociclib capsules should be taken with food. Tablet: When administered with food, AUC and Cmax increased up to 22% and 26%, respectively; food had no significant impact on exposure variability. Palbociclib tablets may be taken with or without food. |
PPB |
85% |
Palbociclib undergoes hepatic metabolism via oxidation and sulfonation, primarily by CYP3A and sulfotransferase (SULT2A1) enzymes; acylation and glucuronidation are minor metabolic pathways.
Inactive metabolites |
Yes |
Half-life |
29 hours (mean plasma) |
Feces |
74% |
Urine |
18% |
- Breast cancer
(Includes conditional approvals)
Refer to the product monograph for a full list and details of approved indications.
Emetogenic Potential:
The following adverse effects occurred in patients with breast cancer treated with palbociclib plus fulvestrant in a Phase III study, where the incidence was at least 2% greater than the placebo plus fulvestrant arm. The table also includes severe or life-threatening adverse effects from other sources or post-marketing.
ORGAN SITE | SIDE EFFECT* (%) | ONSET** | |||
---|---|---|---|---|---|
Cardiovascular | Venous thromboembolism (1%) (pulmonary embolism) | E | |||
Dermatological | Alopecia (15%) | E | |||
Rash, pruritus (14%) | E | ||||
Gastrointestinal | Anorexia (13%) | E | |||
Constipation (17%) | E | ||||
Diarrhea (19%) | E | ||||
Mucositis (25%) | E | ||||
Nausea, vomiting (29%) | E | ||||
General | Edema - limbs (8%) | E | |||
Fatigue (38%) | E | ||||
Hematological | Myelosuppression ± infection, bleeding (79%) (62% severe) | E | |||
Nervous System | Dizziness (11%) | E | |||
Dysgeusia (6%) | E | ||||
Headache (21%) | E | ||||
Insomnia (11%) | E | ||||
Respiratory | Cough, dyspnea (13%) | E | |||
Pneumonitis (1%) | E |
* "Incidence" may refer to an absolute value or the higher value from a reported range.
"Rare"
may refer to events with < 1% incidence, reported in post-marketing, phase 1 studies,
isolated data or anecdotal
reports.
** I = immediate (onset in hours to days)
E = early (days to weeks)
D = delayed (weeks to months)
L = late (months to years)
The most common side effects for palbociclib include myelosuppression ± infection, bleeding, fatigue, nausea, vomiting, mucositis, headache, diarrhea, constipation, alopecia, rash, pruritus and anorexia.
Neutropenia was the most frequently reported adverse effect with a median onset of 15 days. Febrile neutropenia, including one fatal case, has been was reported in 2% of patients across clinical trials.
Infections were reported more frequently. Patients should be warned of the increased risk of infection and promptly report any occurrences of fever to their health care team.
Severe or life-threatening interstitial lung disease/pneumonitis has been reported in combination with endocrine therapy in clinical trials and post-marketing (including fatal cases).
Refer to protocol by which patient is being treated.
Pre- and perimenopausal women treated with palbociclib and an aromatase inhibitor or fulvestrant should also be treated with luteinizing hormone-releasing hormone (LHRH) agonists according to local clinical practice.
in combination with an aromatase inhibitor (e.g., letrozole) or fulvestrant. Refer to regimen monographs for dosing details.
Dose Level |
Palbociclib Dose (mg/day) for 3 out of 4 weeks |
0 | 125 |
-1 | 100 |
-2 | 75 |
-3 | If further dose reduction required, discontinue. |
Toxicity | Grade | Palbociclib Dose |
Hematologic | 3 |
Day 1: Hold and repeat CBC within 1 week. When recovered to Grade ≤ 2, re-start next cycle at same dose. Day 15 of 1st 2 cycles: Continue current dose to complete the cycle. Repeat CBC day 22. If Grade 4 on Day 22, see Grade 4 recommendation below. Consider dose reduction if > 1 week recovery or recurrent Grade 3 neutropenia in subsequent cycles. |
3 with fever ≥ 38.5oC and/or infection | Hold until recovery to Grade ≤ 2. Restart at the next lower dose. | |
4 | Hold until recovery to Grade ≤ 2. Restart at the next lower dose. | |
Symptoms of interstitial lung disease (ILD)/pneumonitis (treatment–related) |
Any | Hold dose and investigate; discontinue if severe ILD confirmed. |
Other non-hematologic | 3 or 4 (if persisting despite medical treatment) | Hold until recovery to Grade ≤ 1 or Grade ≤ 2 (if not considered a safety risk). Restart at the next lower dose. |
Mean fraction of unbound palbociclib in plasma increased with worsening hepatic function.
Hepatic Impairment | Starting Dose |
Mild - Moderate (Child-Pugh class A and B) | No dosage adjustment needed. |
Severe (Child-Pugh class C) | 75 mg once daily (days 1 to 21; q28 days). Monitor for toxicity. |
No adjustment is required for CrCl > 15 mL/min. There is no data available in patients requiring hemodialysis.
No overall differences in efficacy were observed between patients aged 65 and older compared to younger patients. When combined with letrozole, patients ≥ 65 were more likely to experience anemia.
Gender and body weight had no significant effect on drug exposure.
No dose modification is required based on pharmacokinetic, safety and efficacy data across Asian and non-Asian populations.
The safety and efficacy of palbociclib has not been studied in children under 18 years.
- Palbociclib capsules should be administered with food; palbociclib tablets may be given with or without food.
- Capsules or tablets should be swallowed whole and not chewed, crushed, opened, or split prior to administration.
- If a patient vomits or misses a dose, an extra dose should not be taken to make up for the vomited or missed dose. The next dose should be taken at the usual time.
- Grapefruit, pomegranate, starfruit, Seville oranges, their juices or products should be avoided during palbociclib treatment.
- Capsules should be stored at 20 to 25oC, with excursions permitted between 15 to 30oC. Tablets should be stored at 15 to 30oC in original packaging to protect from moisture.
- Patients who are hypersensitive to palbociclib or any ingredient in the formulation or component in the container.
- As fatigue and dizziness have been reported, patients should exercise caution when driving or operating machinery.
- Capsules contain lactose; carefully consider use in patients with hereditary galactose intolerance, severe lactase deficiency or glucose-galactose malabsorption.
Other Drug Properties:
-
Carcinogenicity:
Unknown
An increased incidence of microglial cell tumors was observed male rats; the relevance to humans is unknown.
-
Genotoxicity:
Probable
-
Mutagenicity:
No
-
Fetotoxicity:
Yes
Palbociclib is not recommended for use in pregnancy. Adequate contraception should be used by both sexes during treatment, and for at least 21 days after the last dose (for females) and 97 days after the last dose (for males).
-
Excretion into breast milk:
Unknown
Breastfeeding is not recommended.
-
Fertility effects:
Probable
Animal data suggest that palbociclib may affect male fertility. Sperm preservation should be considered prior to starting treatment in males.
Palbociclib is a substrate and weak inhibitor of CYP3A and a moderate substrate of P-gp. Drug interactions are possible with strong CYP3A inducers and inhibitors. Palbociclib is not an inhibitor of CYP1A2, 2A6, 2B6, 2C9 and 2D6 and not an inducer of CYP1A2, 2B6, 2C8 and 3A4 in vitro.
The drug has a low potential to inhibit drug transporters P-gp, BCRP, OAT1, OAT3, OCT2, OATP1B1 and OATP1B3. Palbociclib is not a substrate of OATP1B1 and OATP1B3 (in vitro studies).
There are no drug interactions with letrozole or goserelin.
Palbociclib solubility is pH dependent. Drug interactions with proton pump inhibitors are minimized when palbociclib capsules are given with food; food also reduces drug exposure variability of palbociclib capsules.
AGENT | EFFECT | MECHANISM | MANAGEMENT |
---|---|---|---|
CYP3A inhibitors (i.e. ketoconazole, clarithromycin, ritonavir, fruit or juice from grapefruit, Seville oranges or starfruit) | ↑ palbociclib concentration and/or toxicity | ↓ metabolism of palbociclib | Avoid strong CYP3A inhibitors. |
Strong and moderate CYP3A inducers (i.e. phenytoin, rifampin, dexamethasone, carbamazepine, phenobarbital, St. John’s Wort, etc) | ↓ palbociclib concentration and/or efficacy | ↑ metabolism of palbociclib | Avoid CYP3A inducers. If use of moderate inducer cannot be avoided, no dose adjustment to palbociclib is needed. |
Antacids and PPIs (e.g. rabeprazole) | ↓ palbociclib exposure when PPI and palbociclib capsules given in fasted conditions; minimal effect when palbociclib capsules given with food | Palbociclib has pH-dependent solubility; reduced palbociclib capsule solubility with increasing pH. | To minimize interaction with antacids and PPIs, palbociclib capsules should be given with food. |
CYP3A substrates (e.g. cyclosporine, pimozide, tacrolimus, triazolo-benzodiazepines, dihydropyridine calcium-channel blockers, certain HMG-CoA reductase inhibitors) | ↑ substrate concentration and/or toxicity | Palbociclib is a weak inhibitor of CYP3A. | Consider reducing the dose of CYP3A substrates with narrow therapeutic indices (e.g. cyclosporine) |
Treating physicians may decide to monitor more or less frequently for individual patients but should always consider recommendations from the product monograph.
Monitor Type | Monitor Frequency |
---|---|
CBC |
Baseline and before each cycle, on day 15 of the first 2 cycles, one week after Grade 3 neutropenia, and as clinically indicated. If neutropenia Grade 2 or less in the first 6 cycles, may monitor every 3rd cycle thereafter |
Liver function tests |
Baseline and as clinically indicated |
Renal function tests |
Baseline and as clinically indicated |
Clinical toxicity assessment for infection, bleeding, thromboembolism, pneumonitis, rash, headache, mucositis, fatigue and GI effects |
At each visit |
Grade toxicity using the current NCI-CTCAE (Common Terminology Criteria for Adverse Events) version
Exceptional Access Program (EAP Website)
- palbociclib - For the treatment of patients with estrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER 2)-negative, unresectable locally advanced or metastatic breast cancer in combination with an aromatase inhibitor or fulvestrant, according to clinical criteria
Finn RS, Crown JP, Lang I, et al. The cyclin-dependent kinase 4/6 inhibitor palbociclib in combination with letrozole versus letrozole alone as first-line treatment of oestrogen receptor-positive, HER2-negative, advanced breast cancer (PALOMA-1/TRIO-18): a randomised phase 2 study. Lancet Oncol. 2015 Jan;16(1):25-35.
Product Monograph: Ibrance (palbociclib). Pfizer Canada Inc. January 24, 2020.
April 2021 Updated indication and dosing description
Refer to the New Drug Funding Program or Ontario Public Drug Programs websites for the most up-to-date public funding information.
The information set out in the drug monographs, regimen monographs, appendices and symptom management information (for health professionals) contained in the Drug Formulary (the "Formulary") is intended for healthcare providers and is to be used for informational purposes only. The information is not intended to cover all possible uses, directions, precautions, drug interactions or adverse effects of a particular drug, nor should it be construed to indicate that use of a particular drug is safe, appropriate or effective for a given condition. The information in the Formulary is not intended to constitute or be a substitute for medical advice and should not be relied upon in any such regard. All uses of the Formulary are subject to clinical judgment and actual prescribing patterns may not follow the information provided in the Formulary.
The format and content of the drug monographs, regimen monographs, appendices and symptom management information contained in the Formulary will change as they are reviewed and revised on a periodic basis. The date of last revision will be visible on each page of the monograph and regimen. Since standards of usage are constantly evolving, it is advised that the Formulary not be used as the sole source of information. It is strongly recommended that original references or product monograph be consulted prior to using a chemotherapy regimen for the first time.
Some Formulary documents, such as the medication information sheets, regimen information sheets and symptom management information (for patients), are intended for patients. Patients should always consult with their healthcare provider if they have questions regarding any information set out in the Formulary documents.
While care has been taken in the preparation of the information contained in the Formulary, such information is provided on an “as-is” basis, without any representation, warranty, or condition, whether express, or implied, statutory or otherwise, as to the information’s quality, accuracy, currency, completeness, or reliability.
CCO and the Formulary’s content providers shall have no liability, whether direct, indirect, consequential, contingent, special, or incidental, related to or arising from the information in the Formulary or its use thereof, whether based on breach of contract or tort (including negligence), and even if advised of the possibility thereof. Anyone using the information in the Formulary does so at his or her own risk, and by using such information, agrees to indemnify CCO and its content providers from any and all liability, loss, damages, costs and expenses (including legal fees and expenses) arising from such person’s use of the information in the Formulary.
Finn RS, Crown JP, Lang I, et al. The cyclin-dependent kinase 4/6 inhibitor palbociclib in combination with letrozole versus letrozole alone as first-line treatment of oestrogen receptor-positive, HER2-negative, advanced breast cancer (PALOMA-1/TRIO-18): a randomised phase 2 study. Lancet Oncol. 2015 Jan;16(1):25-35.
Product Monograph: Ibrance (palbociclib). Pfizer Canada Inc. January 24, 2020.
palbociclib (patient)
Info Sheet Introduction:- For treating certain types of hormone sensitive breast cancer. Palbociclib is given together with another medication.
Other Name: Ibrance™
Tablet or capsule in various strengths and colours
-
For treating certain types of hormone sensitive breast cancer. Palbociclib is given together with another medication.
Tell your health care team if you have or had significant medical condition(s), especially if you have / had:
-
liver or kidney problems,
-
lung problems,
-
active infections, or
-
any allergies.
Palbociclib capsules contain a small amount of lactose. If you cannot tolerate lactose, talk to your health care team.
Remember to:
-
Tell your health care team about all of the other medications you are taking.
-
Keep taking other medications that have been prescribed for you, unless you have been told not to by your health care team.
Talk to your health care team about:
-
How this medication may affect your sexual health.
-
How this medication may affect your ability to have a baby, if this applies to you.
This medication may harm an unborn baby. Tell your health care team if you or your partner are pregnant, become pregnant during treatment, or are breastfeeding.
-
If there is any chance of pregnancy happening, you and your partner together must use 2 effective forms of birth control at the same time until 21 days after your last dose (if you are female) and 97 days after your last treatment dose (if you are male). Talk to your health care team about which birth control options are best for you.
-
Do not use hormonal birth control (such as birth control pills), unless your health care team told you that they are safe. Talk to your health care team about the safest birth control for you.
-
Do not breastfeed while on this medication.
-
This medication is usually taken once a day by mouth for 3 weeks followed by a 1 week break with no palbociclib treatment. Talk to your health care team about how and when to take your medication.
-
Take the dose at about the same time each day.
-
If you have palbociclib tablets, swallow them whole with a glass of water, with or without food.
-
If you have palbociclib capsules, swallow them whole with a glass of water, with food.
-
Do not chew, crush, open, or split the tablets or capsules.
-
If you vomit (throw up) or miss a dose, skip this and take your next dose as you normally do. Do not take an extra dose to make up for the missed dose.
-
If you take too much of your medication by accident, or if you think a child or a pet may have swallowed your medication, you must call the Ontario Poison Control Center right away at: 1-800-268-9017.
Will this medication interact with other medications or natural health products?
-
This medication can interact with other medications, vitamins, foods and natural health products. Interactions can make the treatment not work as well or cause severe side effects.
-
Tell your health care team about all of your:
-
prescription and over-the-counter (non-prescription) medications and all other drugs, such as marijuana (medical or recreational)
-
natural health products such as vitamins, herbal teas, homeopathic medicines, and other supplements
-
-
Check with your health care team before starting or stopping any of them.
What should I do if I feel unwell, have pain, a headache or a fever?
-
Always check your temperature to see if you have a fever before taking any medications for fever or pain (such as acetaminophen (Tylenol®) or ibuprofen (Advil®)).
-
Fever can be a sign of infection that may need treatment right away.
-
If you take these medications before you check for fever, they may lower your temperature and you may not know you have an infection.
-
How to check for fever:
Keep a digital (electronic) thermometer at home and take your temperature if you feel hot or unwell (for example, chills, headache, mild pain).
- You have a fever if your temperature taken in your mouth (oral temperature) is:
- 38.3°C (100.9°F) or higher at any time
OR
- 38.0°C (100.4°F) or higher for at least one hour.
- 38.3°C (100.9°F) or higher at any time
If you do have a fever:
-
Try to contact your health care team. If you are not able to talk to them for advice, you MUST get emergency medical help right away.
-
Ask your health care team for the Fever pamphlet for more information.
If you do not have a fever but have mild symptoms such as headache or mild pain:
-
Ask your health care team about the right medication for you. Acetaminophen (Tylenol®) is a safe choice for most people.
-
Talk to your health care team before you start taking Ibuprofen (Advil®, Motrin®), naproxen (Aleve®) or ASA (Aspirin®), as they may increase your chance of bleeding or interact with your cancer treatment.
-
Talk to your health care team if you already take low dose aspirin for a medical condition (such as a heart problem). It may still be safe to take.
What to DO while on this medication:
-
DO check with your health care team before getting any vaccinations, surgery, dental work or other medical procedures.
What NOT to DO while on this medication:
-
DO NOT smoke or drink alcohol while on treatment without talking to your health care team first. Smoking and drinking can make side effects worse and make your treatment not work as well.
-
DO NOT eat or drink grapefruit, starfruit, pomegranate, Seville oranges or their juices (or products that contain these) while taking this drug. They may increase the amount of drug in your blood and increase side effects.
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DO NOT drive, operate machinery or do any tasks that need you to be alert if you feel tired or dizzy.
-
Do not throw out any unused medications at home. Bring them to your pharmacy to be thrown away safely.
-
Keep this medication in the original packaging at room temperature in a dry place, away from heat and light. Keep out of sight and reach of children and pets.
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How to safely touch oral anti-cancer medications
If you are a patient:
-
Wash your hands before and after touching your oral anti-cancer medication.
-
Swallow each pill whole. Do not crush or chew your pills.
If you are a caregiver:
-
Wear nitrile or latex gloves when touching tablets, capsules or liquids.
-
Wash your hands before putting on your gloves and after taking them off, even if your skin did not touch the oral anti-cancer medication.
-
Throw out your gloves after each use. Do not re-use gloves.
-
Do not touch oral anti-cancer medications if you are pregnant or breastfeeding.
-
-
What to do if oral anti-cancer medication gets on your skin or in your eyes
If medication gets on your skin:
-
Wash your skin with a lot of soap and water.
-
If your skin gets red or irritated, talk to your health care team.
If medication gets in your eyes:-
Rinse your eyes with running water right away. Keep water flowing over your open eyes for at least 15 minutes.
-
The following table lists side effects that you may have when getting palbociclib. The table is set up to list the most common side effects first and the least common last. It is unlikely that you will have all of the side effects listed and you may have some that are not listed.
Read over the side effect table so that you know what to look for and when to get help. Refer to this table if you experience any side effects while on palbociclib.
Very Common Side Effects (50 or more out of 100 people) | |
Side effects and what to do | When to contact health care team |
Low neutrophils (white blood cells) in the blood (neutropenia) When neutrophils are low, you are at risk of getting an infection more easily. Ask your health care team for the Neutropenia (Low white blood cell count) pamphlet for more information. What to look for?
You have a fever if your temperature taken in your mouth (oral temperature) is:
What to do? If your health care team has told you that you have low neutrophils:
If you have a fever: If you have a fever, try to contact your health care team. If you are unable to talk to the team for advice, you must get emergency medical help right away. |
If you have a fever, try to contact your health care team. If you are unable to talk to the team for advice, you MUST get emergency medical help right away. |
Common Side Effects (25 to 49 out of 100 people) | |
Side effects and what to do | When to contact health care team |
Fatigue What to look for?
What to do?
Ask your health care team for the Fatigue pamphlet for more information.
|
Talk to your health care team if it does not improve or if it is severe |
Nausea and vomiting (generallly mild) What to look for?
What to do? To help prevent nausea:
|
Talk to your healthcare team if nausea lasts more than 48 hours or vomiting lasts more than 24 hours or if it is severe |
Anemia (low red blood cells) What to look for?
What to do? If your health care team has told you that you have anemia (low red blood cells):
If it is very bad, your doctor may need to make changes to your treatment regimen.
|
Talk to your health care team if it does not improve or if it is severe |
Mouth sores What to look for?
To help prevent mouth sores:
Ask your health care team for the Oral Care (Mouth Care) pamphlet for more information. |
Talk to your health care team as soon as you notice mouth or lip sores or if it hurts to eat, drink or swallow |
Less Common Side Effects (10 to 24 out of 100 people) | |
Side effects and what to do | When to contact health care team |
Headache What to look for?
What to do?
Ask your health care team for the Pain pamphlet for more information. |
Talk to your health care team if it does not improve or if it is severe |
Low platelets in the blood When your platelets are low, you are at risk for bleeding and bruising. Ask your health care team for the Low Platelet Count pamphlet for more information. What to look for?
What to do? If your health care team has told you that you have low platelets:
If you have signs of bleeding:
If you have bleeding that does not stop or is severe (very heavy), you must get emergency medical help right away. |
Talk to your health care team if you have any signs of bleeding. If you have bleeding that doesn’t stop or is severe (very heavy), you MUST get emergency help right away. |
Diarrhea What to look for?
What to do? If you have diarrhea:
Ask your health care team for the Diarrhea pamphlet for more information.
|
Talk to your health care team if no improvement after 24 hours of taking diarrhea medication or if severe (more than 7 times in one day) |
Constipation What to look for?
What to do? To help prevent constipation:
To help treat constipation:
Ask your health care team for the Constipation Pamphlet for more information. |
Talk to your health care team if it does not improve or if it is severe |
Hair thinning or loss What to look for?
What to do?
|
Talk to your health care team if this bothers you |
Rash; dry, itchy skin What to look for?
What to do? To prevent and treat dry skin:
Rash may be severe in some rare cases and cause your skin to blister or peel. If this happens, get emergency medical help right away. |
Talk to your health care team if it does not improve or if it is severe |
Low appetite What to look for?
What to do?
Ask your health care team for the Loss of Appetite pamphlet for more information. |
Talk to your health care team if it does not improve or if it is severe |
Cough and feeling short of breath What to look for?
What to do?
|
Talk to your health care team. If you are not able to talk to your health care team for advice, and you have a fever or severe symptoms, you MUST get emergency medical help right away |
Dizziness What to look for?
What to do?
|
Talk to your health care team if it does not improve or if it is severe |
Trouble Sleeping Your medications may cause trouble sleeping. It may get better once your body gets used to the medication or when your treatment ends. What to look for?
What to do? Talk to your health care team if it does not improve or if it is severe |
Talk to your health care team if it does not improve or if it is severe |
Other rare, but serious side effects are possible.
If you experience ANY of the following, speak to your cancer health care provider or get emergency medical help right away:
- Pain, swelling and hardening of the vein in an arm or leg.
Who do I contact if I have questions or need help?My cancer health care provider is: ______________________________________________ During the day I should contact:________________________________________________ Evenings, weekends and holidays:______________________________________________
|
Other Notes:
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
February 2021 Updated/Revised info sheet
For more links on how to manage your symptoms go to www.cancercareontario.ca/symptoms.
The information set out in the medication information sheets, regimen information sheets, and symptom management information (for patients) contained in the Drug Formulary (the "Formulary") is intended to be used by health professionals and patients for informational purposes only. The information is not intended to cover all possible uses, directions, precautions, drug interactions or side effects of a certain drug, nor should it be used to indicate that use of a particular drug is safe, appropriate or effective for a given condition.
A patient should always consult a healthcare provider if he/she has any questions regarding the information set out in the Formulary. The information in the Formulary is not intended to act as or replace medical advice and should not be relied upon in any such regard. All uses of the Formulary are subject to clinical judgment and actual prescribing patterns may not follow the information provided in the Formulary.



- palbociclib - For the treatment of patients with estrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER 2)-negative, unresectable locally advanced or metastatic breast cancer in combination with an aromatase inhibitor or fulvestrant, according to clinical criteria
PAL boe SYE klib
Cancer Type: Breast Type of Content: Drug Monograph Status: Null Info Sheet Status: Null Global Date: Jeudi, avril 29, 2021 Universal Date: 2021-05-25 00:00:00 AddThis: Title URL: palbociclib Drug Display Status: Active Revision Summary:Drug Monograph: Updated indication and dosing description
Patient Info Sheet FR: Updated appearance