Les renseignements du Formulaire de médicaments s’adressent aux professionnels de la santé. Il ne s’agit pas d’un avis médical. Certains des renseignements, y compris ceux sur le financement des médicaments anticancéreux, ne s’appliquent pas à tous les patients. Les plans de traitement du cancer sont propres à chaque patient. Si vous êtes un patient, veuillez parler avec votre équipe soignante pour comprendre comment ces renseignements s’appliquent à vous.
XELOX
Small bowel and appendix
Regimen is considered appropriate as part of the standard care of patients; meaningfully improves outcomes (survival, quality of life), tolerability or costs compared to alternatives (recommended by the Disease Site Team and national consensus body e.g. pan-Canadian Oncology Drug Review, pCODR). Recommendation is based on an appropriately conducted phase III clinical trial relevant to the Canadian context OR (where phase III trials are not feasible) an appropriately sized phase II trial. Regimens where one or more drugs are not approved by Health Canada for any indication will be identified under Rationale and Use.
For the adjuvant treatment of stage III and high risk stage II colorectal, small bowel or appendiceal cancer
capecitabine
ODB - General Benefit
(capecitabine)
(ODB Formulary)
| oxaliplatin | 130 mg /m² | IV | Day 1 |
| capecitabine | 1000 mg /m² | PO | BID, Days 1 to 14 |
REPEAT EVERY 21 DAYS
For a total of 8 cycles unless disease progression or unacceptable toxicity occurs
Moderate
No routine prophylaxis for capecitabine
Low
Also refer to CCO Antiemetic Recommendations.
Screen for hepatitis B virus in all cancer patients starting systemic treatment. Refer to the hepatitis B virus screening and management guideline.
Oxaliplatin premedication (prophylaxis for infusion reactions):
- There is insufficient evidence that routine prophylaxis with pre-medications reduces IR rates.
- Consider corticosteroids and H1-receptor antagonists ± H2-receptor antagonists in high-risk patients (i.e. ≥ cycle 6, younger age, female gender, prior platinum exposure, platinum-free interval ≥ 3 years).
Other Supportive Care
- Topical emollients (e.g. hand creams, udder balm) therapy may ameliorate the manifestations of hand-foot syndrome in patients receiving capecitabine.
- Standard antidiarrheal agents (e.g. loperamide) should be initiated, as medically appropriate, as early as possible.
- Patients should be counselled about cold avoidance prior to receiving oxaliplatin, since cold temperatures can precipitate or exacerbate acute neurological symptoms.
Doses should be modified according to the protocol by which the patient is being treated.
Patients should be tested for DPD deficiency before starting treatment with capecitabine. Refer to the DPD Deficiency Guidance for Clinicians for more information.
In patients with unrecognized DPD deficiency, acute, life-threatening toxicity may occur; if acute grade 2-4 toxicity develops, treatment should be stopped immediately and permanent discontinuation considered based on clinical assessment of the toxicities.
Dosage with toxicity
Do not retreat until ANC ≥ 1.5 x 109 /L, platelet counts ≥ 100 x 109 /L and major organ toxicity has resolved to ≤ grade 1.
Oxaliplatin
Neurotoxicity was graded based on the following scales in some adjuvant colorectal cancer trials.
|
Neurotoxicity Grade
|
Description
|
|
1
|
No change
|
|
2
|
Mild paresthesias, loss of deep tendon reflexes
|
|
3
|
Mild or moderate objective sensory loss, moderate paresthesias
|
|
4
|
Severe objective sensory loss or paresthesias that interfere with function
|
|
Toxicity Grade
|
Oxaliplatin Dose^
|
|
Persistent1 Grade 2 neurotoxicity
|
↓ 25%
|
|
Transient1 Grade 3 neurotoxicity
|
↓ 25%
|
|
Persistent1 Grade 3 neurotoxicity or any Grade 4 neurotoxicity
|
Discontinue
|
|
≥ Grade 3 GI toxicity (after prophylaxis) OR
≥ Grade 3 Platelets OR
≥ Grade 3 Neutropenia (including febrile neutropenia)
|
↓ 25%
|
| Sepsis / septic shock | Discontinue |
|
Other ≥ grade 3 related organ toxicity 2
|
Consider ↓ 25%
|
|
Pharyngolaryngeal dysesthesia
|
Hold; then increase duration of infusion to 6 hours3
|
|
Pneumonitis
|
Hold, investigate; discontinue permanently if confirmed.
|
| Anaphylactic-like reaction |
Discontinue
|
|
PRES/RPLS
|
|
| Hemolytic uremic syndrome or any signs of microangiopathic hemolytic anemia | |
| Disseminated intravascular coagulation (DIC) | |
| QT prolongation | |
| Intestinal ischemia or duodenal ulcer | |
| Symptoms of rhabdomyolysis |
^Do not re-treat until the ANC ≥ 1.5 x 109/L and the platelets ≥ 100 x 109/L, GI and neurotoxicities have resolved and other non-hematologic toxicities ≤ grade 1.
1 Transient = >7days - <1 cycle; persistent = ≥ 1 cycle
2 For skin toxicity, reduce capecitabine dose only (see table below)
3 If oxygen saturation is normal, an anxiolytic agent may be given
Capecitabine
Dose modifications are mandatory for gastrointestinal, dermatological toxicity and hyperbilirubinemia. Practitioner may elect not to reduce dose for other toxicities unlikely to become serious or life-threatening.
Missed or omitted doses of capecitabine should not be replaced. Doses should not be re-escalated if reduced for toxicity.
|
Toxicity
|
Action During a Course of Therapy
|
Dose Adjustment for Next Cycle
(% of starting dose)
|
|
Grade 1
|
Maintain dose level
|
Maintain dose level
|
|
Grade 2
1st appearance
2nd appearance
3rd appearance
4th appearance
|
Hold until resolved to ≤ grade 1
Hold until resolved to ≤ grade 1
Hold until resolved to ≤ grade 1
Discontinue treatment permanently
|
100%
75%
50%
Not applicable
|
|
Grade 3
1st appearance
2nd appearance
3rd appearance OR any evidence of Stevens-Johnson syndrome (i.e. sloughing) |
Hold until resolved to ≤ grade 1
Hold until resolved to ≤ grade 1
Discontinue treatment permanently
|
75% 50%
Not applicable
|
|
Grade 4
1st appearance
2nd appearance
|
Discontinue permanently Discontinue permanently
|
Discontinue or
50%
Not applicable
|
Management of Infusion-related reactions:
Also refer to the CCO guideline for detailed description of Management of Cancer Medication-Related Infusion Reactions.
Oxaliplatin:
| Grade | Management | Re-challenge |
| 1 or 2 |
Restart:
|
|
| 3 or 4 |
|
|
* Up to 50% of patients can experience recurrent reactions during re-challenge despite using pre-medications (e.g. corticosteroid and H1/H2-receptor antagonist).
Hepatic Impairment
|
Hepatic Impairment |
Oxaliplatin (% previous dose) |
Capecitabine (% previous dose)* |
|
Mild |
No dose adjustment required |
No starting dose adjustment necessary |
|
Moderate |
||
|
Severe |
No data available |
No data available |
*use capecitabine dose modification table above for hepatotoxicity during treatment
Renal Impairment
|
Creatinine Clearance (mL/min) |
oxaliplatin (% previous dose) |
capecitabine (% previous dose) |
|
51-80 |
No change |
100%, with close monitoring |
|
30-50 |
Caution |
75 % (use with caution) |
|
<30 |
Discontinue |
CONTRAINDICATED |
Dosage in the Elderly
For oxaliplatin, patients ≥ 65 years had a higher incidence of GI toxicity, myelosuppression, syncope and fatigue. No dose adjustments were needed but caution should be exercised.
For capecitabine, older patients are more susceptible to the effects of fluoropyrimidine-based therapies with increased grade 3 / 4 adverse effects, especially when used in combination. Starting dosage adjustment is not recommended, but dose modifications should be performed for toxicity (see tables above).
Dosage based on gender:
Women may be at higher risk of severe (grades 3-4) neutropenia in adjuvant treatment of colorectal cancer.
Refer to oxaliplatin, capecitabine drug monograph(s) for additional details of adverse effects
|
Very common (≥ 50%) |
Common (25-49%) |
Less common (10-24%) |
Uncommon (< 10%), but may be severe or life-threatening |
|
|
|
|
Refer to oxaliplatin, capecitabine drug monograph(s) for additional details
-
Concomitant use with sorivudine or analogues is contraindicated, given the increased risk of capecitabine toxicity (may be fatal). Wait at least 4 weeks after sorivudine (or chemically related analogues) treatment before starting capecitabine.
-
Avoid concomitant administration with phenytoin; capecitabine may increase levels. Monitor phenytoin levels if must be given together.
-
Monitor PT/INR when this treatment is administered with warfarin or other anticoagulants; adjust anticoagulant dose accordingly.
-
Caution with the use of proton pump inhibitors and monitor for reduced effectiveness of capecitabine; consider switching to a magnesium and aluminum hydroxide-containing antacid.
-
Caution and monitor with the coadministration of leucovorin as this may increase capecitabine toxicity.
- Monitor for toxicity when using oxaliplatin with other nephrotoxic drugs, QT -prolonging drugs or drugs associated with rhabdomyolysis.
Refer to oxaliplatin, capecitabine drug monograph(s) for additional details
Administration:
Oxaliplatin
-
Oxaliplatin is administered by intravenous infusion.
-
May be mixed in 250-500 mL bag (D5W only). Do not mix oxaliplatin with NS, chloride containing or alkaline solutions.
-
Administer by slow infusion. Concentration must be between 0.2 to 0.7 mg/mL.
-
Infuse IV over 2 hours. Increasing infusion time to 6 hours may decrease acute toxicity such as pharyngolaryngeal dysesthesia.
-
Do not mix oxaliplatin with other drugs in the same infusion bag or infusion line.
-
If another drug is given before oxaliplatin, flush infusion line with D5W before giving oxaliplatin. Flush the line with D5W after oxaliplatin before giving a subsequent drug.
-
The compatibility of oxaliplatin solution for infusion has been tested with representative, PVC-based, administration sets.
-
Do not use with injection equipment containing aluminum, as this can degrade platinum compounds.
-
Unopened vials should be stored at 15-30°C; protect from light.
Also refer to the CCO guideline for detailed description of Management of Cancer Medication-Related Infusion Reactions.
Capecitabine:
-
Oral self-administration; drug available by outpatient prescription.
-
Doses are given orally approximately 12 hours apart, within 30 minutes after the end of a meal.
-
Swallow tablets whole; do not crush or cut tablets.
-
If a capecitabine dose is missed, skip this and give the next dose at the usual time. Missed or omitted doses should not be replaced.
-
Store tablets at 15ºC to 30ºC in the original package.
Contraindications:
-
Patients who have a known hypersensitivity to capecitabine, 5-fluorouracil, oxaliplatin, other platinum agents (e.g. cisplatin), or any ingredient in the formulation or component of the container
-
Patients with severe renal impairment (CrCl <30 mL/min)
-
Patients who are pregnant or breastfeeding
-
Patients with known near or complete absence of DPD (dihydropyrimidine dehydrogenase) deficiency. Refer to the DPD Deficiency Guidance for Clinicians for more information.
-
Concomitant use with sorivudine or related analogues (i.e. brivudine), given potential fatal drug interaction.
Warnings/Precautions:
-
Patients should be counselled about cold avoidance prior to receiving oxaliplatin, as cold temperatures can precipitate or exacerbate acute neurological symptoms.
-
Oxaliplatin may cause dizziness or visual disturbances in some patients (including transient vision loss); patients should exercise caution when driving or operating machinery.
-
Use with caution in patients with risk factors for dehydration, pre-existing renal dysfunction or on nephrotoxic agents
-
Use with caution in patients with a history of cardiovascular disease as well as patients taking anticoagulants such as warfarin (see Drug Interactions section)
-
Use capecitabine with extreme caution in patients with partial DPD deficiency. Refer to the DPD Deficiency Guidance for Clinicians for more information.
-
Capecitabine contains lactose and should not be used in patients with hereditary galactose/glucose/lactase disorders.
Pregnancy/Lactation:
-
This regimen is contraindicated for use in pregnancy. Adequate contraception should be used by patients and their partners while on treatment and after the last treatment dose. Recommended methods and duration of contraception may differ depending on the treatment. Refer to the drug monograph(s) for more information.
-
Breastfeeding is contraindicated during this treatment and after the last treatment dose. Refer to the drug monograph(s) for recommendations after the last treatment dose (if available).
-
Fertility effects: Yes
Treating physicians may decide to monitor more or less frequently for individual patients but should always consider recommendations from the product monograph.
Refer to the hepatitis B virus screening and management guideline for monitoring during and after treatment.
Recommended Clinical Monitoring
- CBC; Baseline and before each cycle
- Liver and renal function tests; Baseline and before each cycle
- Electrolytes, including magnesium; Baseline and before each cycle
- INR and/or PT; Baseline and as clinically indicated if on anticoagulants
- Clinical toxicity assessment of GI effects, dehydration, neurotoxicity, infection, bleeding, thromboembolism, hypersensitivity, injection site reaction, rash, hand-foot syndrome, cardiac, respiratory and ophthalmic effects; At each visit
-
Grade toxicity using the current NCI-CTCAE (Common Terminology Criteria for Adverse Events) version
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Outpatient prescription for home administration (capecitabine)
Capecitabine and oxaliplatin drug monographs, Cancer Care Ontario.
Haller DG, Tabernero J, Maroun J, et al. Capecitabine plus oxaliplatin compared with fluorouracil and folinic acid as adjuvant therapy for stage III colon cancer. J Clin Oncol 2011 Apr 10;29(11):1465-71.
National Comprehensive Cancer Network. Colon Cancer (Version 2.2017). https://www.nccn.org/professionals/physician_gls/pdf/colon.pdf. Accessed June 30, 2017.
Pectasides D, Karavasilis V, Papaxoinis G, Gourgioti G, Makatsoris T, Raptou G, et al. Randomized phase III clinical trial comparing the combination of capecitabine and oxaliplatin (CAPOX) with the combination of 5-fluorouracil, leucovorin and oxaliplatin (modified FOLFOX6) as adjuvant therapy in patients with operated high-risk stage II or stage III colorectal cancer. BMC Cancer. 2015;15:384.
Schmoll H-J, Tabernero J, Maroun J, et al. Capecitabine Plus Oxaliplatin Compared With Fluorouracil/Folinic Acid As Adjuvant Therapy for Stage III Colon Cancer: Final Results of the NO16968 Randomized Controlled Phase III Trial. J Clin Oncol 2015 Nov 10;33(32):3733-40.
November 2023 Modified Pregnancy/lactation section
Regimen Abstracts
A Regimen Abstract is an abbreviated version of a Regimen Monograph and contains only top level information on usage, dosing, schedule, cycle length and special notes (if available). It is intended for healthcare providers and is to be used for informational purposes only. It is not intended to constitute or be a substitute for medical advice, and all uses of the Regimen Abstract are subject to clinical judgment. 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, and Cancer Care Ontario disclaims all liability for the use of this information, and for any claims, actions, demands or suits that arise from such use.
Information in regimen abstracts is accurate to the extent of the ST-QBP regimen master listings, and has not undergone the full review process of a regimen monograph. Full regimen monographs will be published for each ST-QBP regimen as they are developed.
Regimen Monographs
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.