Gemzar - Product Information
|Manufacture:||Eli Lilly and Company|
|Condition:||Bladder Cancer, Cervical Cancer, Non-Small Cell Lung Cancer, Ovarian Cancer, Pancreatic Cancer|
|Form:||Liquid solution, Intravenous (IV)|
|Ingredients:||GEMZAR 1 g contains the active ingredient, gemcitabine hydrochloride, equivalent to 1 g of gemcitabine.|
GEMZAR (gemcitabine hydrochloride) is 2'-deoxy-2', 2' - difluorocytidine monohydrochloride (ß-isomer). It has a molecular formula of C9H12F2N3O4•HCl and molecular weight of 299.66. The structural formula is:
Gemcitabine is a white to off-white lyophilised powder to be reconstituted for intravenous use. Each vial contains gemcitabine hydrochloride and other excipients, mannitol and sodium acetate.
Gemcitabine exhibits significant cytotoxicity activity against a variety of cultured murine and human tumour cells. It exhibits cell phase specificity, primarily killing cells undergoing DNA synthesis (S-phase) and under certain conditions blocking progression of cells through the GI/S-phase boundary. In vitro the cytotoxic action of gemcitabine is both concentration and time dependent.
In animal tumour models, the antitumour activity of gemcitabine is schedule dependent. When administered daily gemcitabine causes death in animals with minimal antitumour activity. However, when an every third or fourth day dosing schedule is used, gemcitabine can be given at non-lethal doses and have excellent antitumour activity against a broad range of mouse tumours.
Mechanism of Action
Gemcitabine (dFdC) is metabolised intracellularly by nucleoside kinases to the active diphosphate (dFdCDP) and triphosphate (dFdCTP) nucleosides. The cytotoxic action of gemcitabine appears to be due to inhibition of DNA synthesis by two actions of dFdCDP and dFdCTP. First, dFdCDP inhibits ribonucleotide reductase which is uniquely responsible for catalyzing the reactions that generate the deoxynucleoside triphosphates for DNA synthesis. Inhibition of this enzyme by dFdCDP causes a reduction in the concentrations of deoxynucleosides in general, and especially in that of dCTP. Second, dFdCTP competes with dCTP for incorporation into DNA. Likewise, a small amount of gemcitabine may also be incorporated into RNA. Thus, the reduction in the intracellular concentration of dCTP potentiates the incorporation of dFdCTP into DNA. DNA polymerase epsilon is essentially unable to remove gemcitabine and repair the growing DNA strands. After gemcitabine is incorporated into DNA, one additional nucleotide is added to the growing DNA strands. After this addition there is essentially a complete inhibition in further DNA synthesis (masked chain termination). After incorporation into DNA, gemcitabine then appears to induce the programmed cellular death process known as apoptosis.
The pharmacokinetics of gemcitabine have been examined in 353 patients in seven studies. The 121 women and 232 men ranged in age from 29 to 79 years. Of these patients, approximately 45% had non-small cell lung cancer and 35% were diagnosed with pancreatic cancer. The following pharmacokinetic parameters were obtained for doses ranging from 500 to 2592 mg/m2 that were infused from 0.4 to 1.2 hours. Peak plasma concentrations (obtained within 5 minutes of the end of the infusion) ranged from 3.2 to 45.5 µg/mL. Volume of distribution of the central compartment: 12.4 L/m2 for women and 17.5 L/m2 for men (inter-individual variability was 91.9%). Volume of distribution of the peripheral compartment: 47.4 L/m2. The volume of the peripheral compartment was not sensitive to gender. Plasma protein binding was negligible. Systemic clearance ranged from 29.2 L/hr/m2 to 92.2 L/hr/m2 depending on gender and age (inter-individual variability was 52.2%). These effects result in inter-patient differences in the plasma concentration of gemcitabine and its rate of elimination from the systemic circulation (reflected by differences in half life). Clearance for women is approximately 25% lower than the values for men. Although rapid, clearance for both men and women appears to decrease with age. For the recommended gemcitabine dose of 1000 mg/m2 given as a 30 minute infusion, lower clearance values for women and men should not necessitate a decrease in the gemcitabine dose. The mean renal clearance is 2 - 7 L/hr/m2 with less than 10% excreted as unchanged drug. Half life ranged from 42 to 94 minutes depending on age and gender. For the recommended dosing schedule, gemcitabine elimination should be virtually complete within 5 to 11 hours of the start of the infusion. Gemcitabine does not accumulate when administered once weekly.
Gemcitabine is rapidly metabolised by cytidine deaminase in the liver, kidney, blood and other tissues. Intracellular metabolism of gemcitabine produces the gemcitabine mono, di and triphosphates (dFdCMP, dFdCDP and dFdCTP) of which dFdCDP and dFdCTP are considered active. These intracellular metabolites have not been detected in plasma or urine. The primary metabolite 2' - deoxy-2', 2’-difluorouridine (dFdU), is not active and is found in plasma and urine.
This metabolite can be found in peripheral blood mononuclear cells and the information below refers to these cells.
Half-life of terminal elimination: 0.7 - 12 hours.
Intracellular concentrations increase in proportion to gemcitabine doses of 35 - 350 mg/m2/30 min, which give steady state concentrations of 0.4 - 5 µg/mL. At gemcitabine plasma concentrations above 5 µg/mL, dFdCTP levels do not increase, suggesting that the formation is saturable in these cells. Parent plasma concentrations following a dose of 1,000 mg/m2/30 min are greater than 5 µg/mL for approximately 30 minutes after the end of the infusion, and greater than 0.4 µg/mL for an additional hour.
Peak plasma concentrations (3 - 15 minutes after end of 30 minute infusion, 1,000 mg/m2): 28 - 52 µg/mL.
Trough concentration following once weekly dosing: 0.07 - 1.12 µg/mL, with no apparent accumulation.
Triphasic plasma concentration versus time curve, mean half life of terminal phase - 65 hours (range 33 - 84 hr).
Formation of dFdU from parent compound: 91% - 98%.
Mean volume of distribution of central compartment: 18 L/m2 (range 11 - 22 L/m2).
Mean steady state volume of distribution (Vss): 150 L/m2 (range 96 - 228 L/m2).
Tissue distribution: extensive.
Mean apparent clearance: 2.5 L/hr/m2 (range 1 – 4 L/hr/m2).
Urinary excretion: all.
Amount recovered in one week: 92% - 98%, of which 99% is dFdU, 1% of the dose is excreted in faeces.
Non Small Cell Lung Cancer (NSCLC)
Four phase 2 single agent studies were conducted with the primary endpoint being tumour response and a secondary measure of symptomatic improvement. The studies were conducted using gemcitabine doses from 800-1250 mg/m2 as a single agent. The three major studies conducted resulted in uniform response rates from 19.7 - 22.5% of evaluable patients and from 17.9 - 20.5% on an intent to treat based analysis after assessment by external peer review boards. The median response duration was 7.6 to 12.7 months, while the overall median survival (for responders and non responders) was from 8.1 to 9.2 months. The major study conducted had 3 patients (2%) achieve complete response and 30 patients (20%) experience partial response out of 151 patients. The fourth trial which was much smaller, with only a total of 34 patients. The mean effective patient dose in this smaller trial was 741 mg/m2 which was lower than that in the 3 major studies (≥ 960 mg/m2), with a tendency towards dose reduction rather than dose incrementing. A response rate of 1 patient (3.2%) out of 31 evaluable patients was observed. The following shows an integrated summary of adverse events (events that occurred in ≥ causality assessment) for the 4 pivotal trials (n=360): dyspnoea = 7.5% (27), anaemia = 6.9% (25), fever = 4.2% (15), nausea = 3.9% (14), vomiting = 3.3% (12), carcinoma of lung = 3.1% (11), pain = 2.5% (9), pneumonia = 2.5% (9), dehydration = 2.2% (8), pleural effusion = 2.2% (8) and discontinuation due to progressive disease = 53.6% (193).
A total of 522 patients were enrolled in a phase 3 randomised trial to receive gemcitabine plus cisplatin (GC) (260) or single agent cisplatin (262) over a 4-week schedule. The median survival was 9.1 months (95% CI 8.3 to 10.6 months) for the GC-treated patients, which was significantly superior to cisplatin-treated patients [7.6 months (95% CI 6.5 to 8.2 months)] (p=0.0040). The estimate of median time to disease progression was 5.6 months (95% CI of 4.6 to 6.1 months) for GC-treated patients, which was significantly superior to cisplatin-treated patients [3.7 months (95% CI 3.3 to 4.2 months)] (p=0.0013). The overall response rate was 30.4% for GC-treated patients and 11.1% for patients treated with single agent cisplatin (p<0.0001).
A total of 135 patients were enrolled in a phase 3 randomised trial to receive GC (69) or cisplatin plus etoposide (66) over a 3-week schedule. The median survival was 8.7 months (95% CI 7.7 to 10.2 months) for the GC arm and 7.2 months (95% CI 6.1 to 9.8 months) for the patients treated with cisplatin plus etoposide, which was not significantly different. The estimate of median time to disease progression was 6.9 months (95%CI of 5.0 to 8.1 months) for GC-treated patients, which was significantly superior to cisplatin plus etoposide treated patients [4.3 months (95% CI 3.5 to 4.7 months)] (p=0.0147). The overall response rate (intent-to-treat) was 40.6% for GC-treated patients and 21.2% for patients treated with cisplatin plus etoposide (p=0.0167).
Data from two clinical trials evaluated the use of GEMZAR in patients with locally advanced or metastatic pancreatic cancer. The first trial compared GEMZAR to 5-FU in patients who had received no prior chemotherapy. A second trial studied the use of GEMZAR in pancreatic cancer patients previously treated with 5-FU or a 5-FU containing regimen.
The primary efficacy parameter in these studies was clinical benefit response. Clinical benefit response is a measure of symptomatic improvement. When these studies were being conducted, a standard validated quality of life instrument was not available for the assessment of patients with pancreatic cancer. Clinical benefit is a measure of clinical improvement based on analgesic consumption, pain intensity, performance status and weight change. Definitions for improvement in these variables were formulated prospectively during the design of the two trials. A patient was considered a clinical responder if either:
- the patient showed a > 50% reduction in pain intensity (Memorial Pain Assessment) or analgesic consumption, or a twenty point or greater improvement in performance status (Karnofsky Performance Scale) for a period of at least four consecutive weeks, without showing any sustained worsening in any of the other parameters. Sustained worsening was defined as four consecutive weeks with either an increase in pain intensity or analgesic consumption or a 20 point decrease in performance status occurring during the first 12 weeks of therapy or
- the patient was stable on all the aforementioned parameters, and showed a marked, sustained weight gain (≥ 7% increase maintained for ≥ 4 weeks), not due to fluid accumulation.
The first study was a multicenter, prospective, single-blinded, two arm, randomised comparison of GEMZAR and 5FU in patients with locally advanced or metastatic pancreatic cancer who had received no prior treatment with chemotherapy. 5-FU was administered intravenously at a weekly dose of 600mg/m2 for 30 minutes. The results for this randomised trial are shown in Table 1. Compared to 5-FU, patients treated with GEMZAR had statistically significant increase in symptomatic improvement, survival and time to progressive disease (23.8% vs 4.8%).
|Number of patients||63||63||Total: 126|
|Stage IV disease||71.4%||76.2%|
|Baseline KPS ≤ 70||69.8%||68.3%|
|Clinical Response1||23.8% (N=15)||4.8% (N=3)||p=0.0022|
|Median||5.7 months||4.2 months|
|6 month probability||46% (N=30)||29% (N=19)|
|9 month probability||24% (N=14)||5% (N=4)|
|1 year probability||18% (N=9)||2% (N=2)|
|Range||0.2 to 18.6 months||0.4 to 15.1+ months|
|Time to progressive disease||p= 0.0013|
|Median||2.1 months||0.9 months|
|Range||0.1+ to 9.4 months||0.1 to 12.0+ months|
(1 as per previous definition, + = no progression of disease at last visit, still alive)
The second trial was a multicenter, open-label study of 63 patients with advanced pancreatic cancer previously treated with 5-FU or a 5-FU containing regimen. In this study, 27% of the 63 patients who had failed 5FU combinations showed, with GEMZAR; a clinical benefit response and a median survival of 3.8 months.
A total of 405 patients were randomised in a phase 3 trial to receive gemcitabine plus cisplatin (GC) or MVAC (methotrexate, vinblastine, adriamycin, cisplatin). Two hundred patients received GC (gemcitabine 1000 mg/m2 on Days 1, 8 and 15; cisplatin 70 mg/m2 on Day 2) administered intravenously over a 28 day period or MVAC (methotrexate, 30 mg/m2 on Days 1, 15 and 22; vinblastine 3 mg/m2 on Days 2, 15 and 22; adriamycin 30 mg/m 2 on Day 2; cisplatin 70 mg/m2 on Day 2) administered intravenously over a 28 day period. The median overall survival was 12.8 months (95% CI 12.0 to 15.3 months) for patients treated with GC and 14.8 months (95% CI 13.2 to 17.2 months) for MVAC-treated patients, which was not statistically significantly different. The probability of surviving beyond 12 months was estimated as 57% for the GC arm and 62% for the MVAC arm. Median time to progressive disease was 7.4 months (95% CI 6.6 to 8.1 months) for GC-treated patients and 7.6 months (95% CI 6.7 to 9.1 months) for MVAC-treated patients, which was not statistically significantly different. The independently reviewed, overall response rate was 49.4%, (95% CI 41.7%-57.1%) in the GC arm and 45.7 % (95% CI 37.7 to 53.7) in the MVAC arm (p=0.512). The median duration of response was 9.6 months (95% CI 8.0 to 10.8 months) for GC-treated patients and 10.7 months (95% CI 9.4 to 12.6 months) for MVAC-treated patients, which was not statistically significantly different.
Phase 2 trials were conducted using single agent gemcitabine, administered at doses of 1200 or 1250 mg/m2 given weekly for 3 out of every 4 weeks. The response rates were 23% (95% CI 9.6 - 41.2%), 24% (95% CI 11.8 - 41.1%) and 22% (95% CI 9.8 – 38.2%). The median survivals were 9.3 months (95% CI 4.9 – 14.9 months), 12.5 months (95% CI 9.4 – 14.6 months) and 7.9 months (95% CI 5.8 – 11.6 months).
Data from a pivotal study support the use of GEMZAR in combination with paclitaxel for the treatment of patients with unresectable, locally recurrent or metastatic breast cancer who have relapsed following adjuvant anthracycline based chemotherapy. In this multicentre, open-label, randomised Phase 3 study, a total of 529 female patients with unresectable, recurrent or metastatic breast cancer were randomised to receive gemcitabine plus paclitaxel (GT) combination therapy (n= 266) or paclitaxel (T) monotherapy (n=263). In the GT arm gemcitabine (1250 mg/m2) was administered intravenously over 30 to 60 minutes on Days 1 and 8 of a 21-day cycle and paclitaxel (175 mg/m2) was administered intravenously over 3 hours before gemcitabine on Day 1 of a 21-day cycle. In the T arm paclitaxel (175 mg/m2) was administered intravenously over 3 hours on Day 1 of a 21-Day cycle. Patients were included in the trial if they had relapsed after receiving either one anthracycline-based chemotherapy in the adjuvant/neoadjuvant setting or a non-anthracycline-based regimen in the adjuvant/neoadjuvant setting if use of an anthracycline was clinically contraindicated.
The study objectives were to compare overall survival, time to documented disease progression (TtDPD), progression-free survival (PFS), response rates, duration of response, and toxicities between patients treated with GEMZAR plus paclitaxel combination therapy and those treated with paclitaxel monotherapy.
The primary endpoint of the planned interim analysis was time to documented progression of disease (TtDPD). Patients who died without evidence of disease progression were excluded from this analysis. Estimates of median TtDPD were 5.4 months (95% CI, 4.6 to 6.1 months) on the GT therapy arm and 3.5 months (95% CI, 2.9 to 4.0 months) on the T arm using the earlier of the dates of disease progression, derived from either the investigator’s or the independent reviewers’ assessment. The difference between the two treatment arms was statistically significant (p=0.0013). GT also significantly improved progression-free survival by a similar amount. This endpoint accounts for not only patients with documented disease progression but also patients who died without evidence of progression.
Median Overall Survival analysis showed statistically significant improvement in the GEMZAR plus paclitaxel arm compared with the paclitaxel alone arm, as demonstrated by a longer median survival (18.6 versus 15.8 months, with a hazard ratio of 0.82 (95% confidence interval [CI], 0.67 to 1.00, log-rank p=0.05).
The overall response rates, according to the investigator assessment were 39.3% (95% CI, 33.5% to 45.2%) on the GT arm and 25.6% (95% CI, 20.3% to 30.9%) on the T arm, which was statistically significant (p=0.0007). Overall best study response as determined by independent review for a subset of 382 patients (72% of total patients) confirmed that GT-treated patients had statistically significant improvement in overall response compared with patients treated with T monotherapy.
There were no significant treatment differences in the patient-assessed quality-of-life measures, Brief Pain Inventory and Rotterdam Symptom Checklist.
A total of 356 patients with advanced epithelial ovarian cancer who had failed first-line platinum-containing therapy at least 6 months after treatment discontinuation were randomised to receive gemcitabine plus carboplatin (GCb) (178) or carboplatin (Cb) (178). Patients received either GCb (gemcitabine 1000 mg/m2 on Days 1 and 8 and carboplatin administered after gemcitabine on Day 1 with a target AUC of 4.0 mg/mL) or Cb (target AUC of 5.0 mg/mL administered on Day 1) every 21 days until disease progression or until a maximum of six cycles of treatment had been given.
Patients on the GCb arm had a statistically significant improvement in Time to Progressive Disease (TtPD) compared with those on the Cb arm (hazard ratio, 0.72; 95% CI, 0.57 to 0.90; log-rank p-value=0.0038) with a median TtPD of 8.6 months (95% CI, 8.0 to 9.7 months) on the GCb arm versus 5.8 months (95% CI, 5.2 to 7.1 months) on the Cb arm. Patients on the GCb arm had a statistically significant improvement in Time to Treatment Failure (TtTF) compared with those on the Cb arm (hazard ratio 0.74, 95% CI, 0.60 to 0.92; log-rank p-value=0.0072). The median TtTF was 7.0 months (95% CI, 5.8 to 8.1 months) on the GCb arm and 4.8 months (95% CI, 4.1 to 5.6 months) on the Cb arm.
Median overall survival was 18.0 months (95% CI, 16.2-20.2) for GCb arm and 17.3 months (95% CI, 15.2-19.3) for the Cb arm (hazard ratio 0.96, 95% CI 0.75 – 1.23). The trial was not powered to detect an effect on overall survival and treatments received after completion of study therapy were not balanced between arms.
GEMZAR is indicated for treatment of patients with locally advanced or metastatic non-small cell lung cancer.
GEMZAR is indicated for treatment of patients with locally advanced or metastatic adenocarcinoma of the pancreas. GEMZAR is also indicated for patients with 5-FU refractory pancreatic cancer.
GEMZAR, alone or in combination with cisplatin, is indicated for treatment of patients with bladder cancer.
GEMZAR, in combination with paclitaxel, is indicated for the treatment of patients with unresectable, locally recurrent or metastatic breast cancer who have relapsed following adjuvant/neoadjuvant chemotherapy. Prior chemotherapy should have included an anthracycline unless clinically contraindicated.
GEMZAR, in combination with carboplatin, is indicated for the treatment of patients with recurrent epithelial ovarian carcinoma, who have relapsed > 6 months following platinum– based therapy.
Gemcitabine is contraindicated in those patients with a known hypersensitivity to the drug.
Prolongation of the infusion time and the increased dosing frequency have been shown to increase toxicity. In common with other cytotoxic agents, gemcitabine has demonstrated the ability to suppress the bone marrow. Leucopenia, thrombocytopenia and anaemia are expected adverse events. However, myelosuppression is short lived.
Gemcitabine has been reported to cause somnolence. Patients should be cautioned against driving or operating machinery until it is established that they do not become somnolent.
Reports of haemolytic uraemic syndrome (HUS), capillary leak syndrome (CLS), adult respiratory distress syndrome (ARDS), and posterior reversible encephalopathy syndrome (PRES) with potentially severe consequences have been reported in patients receiving gemcitabine as single agent or in combination with other chemotherapeutic agents. These events can be related to vascular endothelial injury possibly induced by gemcitabine. Gemcitabine should be discontinued and supportive measures implemented if any of these develop during therapy. (see Adverse Reactions).
In addition to ARDS, other severe pulmonary effects such as interstitial pneumonitis and pulmonary oedema have been reported in patients receiving gemcitabine as single agent or in combination with other chemotherapeutic agents. Gemcitabine should be discontinued and supportive measures provided if these effects develop during therapy (see Adverse Reactions).
Patients receiving therapy with gemcitabine must be monitored closely. Laboratory facilities should be available to monitor drug tolerance. Resources to protect and maintain a patient compromised by drug toxicity may be required.
Interstitial pneumonitis together with pulmonary infiltrates has been seen in less than 1% of the patients. In such cases, Gemzar treatment must be stopped. Steroids may relieve the symptoms in such situations. Severe rarely fatal pulmonary effects, such as pulmonary oedema, interstitial pneumonitis and acute respiratory distress syndrome (ARDS) have been reported as less common or rare. In such cases, cessation of Gemzar treatment is necessary. Starting supportive treatment at an early stage may improve the situation.
Category D. Cytotoxic agents can produce spontaneous abortion, foetal loss and birth defects. Gemcitabine must not be used during pregnancy. Studies in experimental animals (mice and rabbits at doses up to 4.5 and 1.6 mg/m2 /day IV respectively, administered during the period of organogenesis) have shown teratogenicity and embryotoxicity. Peri and post-natal studies in mice at doses up to 4.5 mg/m2 /day have shown retarded physical development in the offspring. Women of childbearing age receiving gemcitabine should be advised to avoid becoming pregnant, and to inform the treating physician immediately should this occur.
It is not known whether the drug is excreted in human milk, however, studies in lactating rats have shown gemcitabine and/or its metabolites in the milk 10 minutes after an IV dose to the dam. The use of gemcitabine should be avoided in nursing women because of the potential hazard to the infant.
Therapy should be started cautiously in patients with compromised bone marrow function. As with other oncolytics, the possibility of cumulative bone marrow suppression when using combination or sequential chemotherapy should be considered.
Patients receiving gemcitabine should be monitored prior to each dose for platelet, leucocyte and granulocyte counts. Suspension or modification of therapy should be considered when drug-induced marrow depression is detected. For guidelines regarding dose modifications (see Dosage and Administration). Peripheral blood counts may continue to fall after the drug is stopped.
Laboratory evaluation of renal and hepatic function should be performed periodically. Raised liver transaminases [aspartate aminotransferase (AST) and / alanine aminotransferase (ALT)] and alkaline phosphatase are seen in approximately 60% of the patients. These increases are usually mild, transient and not progressive, and seldom lead to cessation of treatment (see Adverse Reactions). Increased bilirubin (WHO toxicity degrees 3 and 4) was observed in 2.6% of the patients. Gemcitabine should be given with caution to patients with impaired hepatic function.
Administration of gemcitabine in patients with concurrent liver metastases or a pre-existing medical history of hepatitis, alcoholism or liver cirrhosis may lead to exacerbation of the underlying hepatic insufficiency.
A few cases of renal failure, including haemolytic uraemic syndrome have been reported (see Aadverse Reactions). Gemcitabine should be administered with caution to patients with impaired renal function. Gemzar treatment should be withdrawn if there is any sign of micro-angiopathic haemolytic anaemia, such as rapidly falling haemoglobin levels with simultaneous thrombocytopenia, elevation of serum bilirubin, serum creatinine, urea or LDH. Renal failure may be irreversible despite withdrawal of the Gemzar treatment and may require dialysis.
Interactions With Other Medications
Concurrent (given together or ≤7 days apart) – Toxicity associated with this multimodality therapy is dependent on many different factors, including dose of gemcitabine, frequency of gemcitabine administration, dose of radiation, radiotherapy planning technique, the target tissue and target volume. In a single trial where gemcitabine at a dose of 1,000 mg/m2 was administered concurrently for up to 6 consecutive weeks with therapeutic thoracic radiation to patients with non-small cell lung cancer, significant toxicity in the form of severe, and potentially life-threatening, oesophagitis and pneumonitis was observed, particularly in patients receiving large volumes of radiotherapy [median treatment volumes 4,795 cm3]. The optimum regimen for safe administration of gemcitabine with therapeutic doses of radiation has not yet been determined.
Radiation injury has been reported on targeted tissues (e.g. oesophagitis, colitis and pneumonitis) in association with both concurrent and non-concurrent use of gemcitabine.
When given in combination with paclitaxel, cisplatin, or carboplatin, the pharmacokinetics of gemcitabine were not altered. Gemcitabine had no effect on paclitaxel pharmacokinetics.
The most commonly reported adverse drug reactions associated with Gemzar treatment include: nausea with or without vomiting; raised liver transaminases (AST/ALT) and alkaline phosphatase, reported in approximately 60% of patients; proteinuria and haematuria reported in approximately 50% patients; dyspnoea reported in 10 – 40% of patients (highest incidence in lung cancer patients); and allergic skin rashes, which occur in approximately 25% of patients and are associated with itching in 10% of patients.
The frequency and severity of the adverse reactions are affected by the dose, infusion rate and intervals between doses (see Warnings). Dose-limiting adverse reactions are reductions in platelet, leucocyte and granulocyte counts (see Dosage and Administration - Dose Reduction).
Slightly higher frequencies of serious adverse events were observed in females, reflecting the gender differences in pharmacokinetic parameters (see Pharmacology - Pharmacokinetic Properties). However, the pattern was inconsistent, with some events being more frequently reported for males than females. In analysis of WHO toxicity no important differences were observed, although slightly higher frequencies of haematologic toxicity were found in females.
|System Organ Class|
|Blood and Lymphatic System Disorders||Very Common|
Leucopenia, thrombocytopenia, anaemia, (Neutropenia Grade 3=19.3%; Grade 4=6%)
|Immune System Disorders||Very Rare|
Anaphylactoid reaction (see Contraindications)
|Nervous System Disorders||Common|
Posterior reversible encephalopathy syndrome (see Warnings)
Myocardial infarct, heart failure, arrhythmia (predominantly supraventricular in nature)
Peripheral vasculitis and gangrene, and capillary leak syndrome (see Warnings)
|Respiratory, Thoracic, and Mediastinal Disorders||Very Common|
Pulmonary oedema, bronchospasm, interstitial pneumonitis (see Precautions)
Adult Respiratory Distress Syndrome (see Warnings and Precautions)
|Gastrointestinal Disorders||Very common|
|Hepatobiliary Disorders||Very Common|
Elevation of liver transaminases (AST/ALT) and alkaline phosphatase (see Precautions)
Increased bilirubin (see Precautions)
Elevation of gamma-glutamyl transferase (GCT)
|Skin and Subcutaneous Tissue Disorders||Very common|
Allergic skin rash, frequently associated with pruritus
Alopecia, ulceration of mucous membrane of the mouth, itching
Scaling, vesicle and sore formation, ulceration
Severe skin reactions, including desquamation and bullous skin eruptions
|Renal and Urinary Disorders||Very Common|
Mild proteinuria, haematuria
Renal failure, haemolytic uraemic syndrome (see Precautions)
|General Disorders and Administration Site Conditions||Very Common|
Oedema/peripheral oedema, Influenza-like symptoms - the most common symptoms are fever, headache, back-pain, shivering, muscle pain, asthenia and anorexia. Cough, rhinitis, perspiration, malaise and sleeping difficulties have also been reported.
|Injury, Poisoning and Procedural Complications||Radiation Toxicity and Radiation Recall (see Precautions - Interactions)|
Frequencies: Very common: ≥ 10%; Common: ≥ 1% and < 10%; Uncommon: ≥ 0.1% and < 1%; Rare: ≥ 0.01% and < 0.1%; Very rare: <0.01%
Gemcitabine Plus Cisplatin
An increase was seen in the following Grade 3 and 4 events (gemcitabine + cisplatin vs MVAC (methotrexate, vinblastine, doxorubicin, and cisplatin)) as follows:
|Gemcitabine + Cisplatin||MVAC|
|Haematological toxicity||Grade 3||Grade 4||Grade 3||Grade 4|
|Nausea and Vomiting||22%||0||19%||2%|
Gemcitabine Plus Paclitaxel
An increase was seen in the following Grade 3 and 4 events (gemcitabine + paclitaxel vs paclitaxel alone) as follows:
|Gemcitabine + Paclitaxel||Paclitaxel|
|Haematological toxicity||Grade 3||Grade 4||Grade 3||Grade 4|
Gemcitabine Plus carboplatin
An increase was seen in the following Grade 3 and 4 events (gemcitabine + carboplatin vs carboplatin alone) as follows:
|Gemcitabine + Carboplatin||Carboplatin|
|Haematological toxicity||Grade 3||Grade 4||Grade 3||Grade 4|
|Infection without neutropenia||0.6%||0||0||0|
In repeat dose studies of up to 6 months duration in mice and dogs, the principal finding was haematopoietic suppression. These effects were related to the cytotoxic properties of the drug and were reversible when treatment was withdrawn. The degree of the effect was schedule and dose-dependent.
Carcinogenesis, Mutagenesis, Fertility
Cytogenetic damage has been produced by gemcitabine in an in vivo assay. Gemcitabine induced forward mutation in vitro in a mouse lymphoma (L5178Y) assay. Long term animal studies have not been conducted to evaluate the carcinogenic potential of gemcitabine.
Gemcitabine caused a dose and schedule dependent hypospermatogenesis in male mice (0.9 mg/m2 /day or 10.5 mg/m 2 weekly administration IP). Although animal studies have shown an effect of gemcitabine on male fertility (1.5 mg/m2/day IP or 30 mg/m2 IP weekly), no effect has been seen on female fertility (up to 4.5 mg/m2/day IV).
Dosage and Administration
Non-small Cell Lung Cancer
The optimum dose schedule for gemcitabine has not been determined. The recommended dose of gemcitabine is 1,000 mg/m2, given by 30 minute intravenous infusion. This should be repeated once weekly for three weeks, followed by a one week rest period. This four week cycle is then repeated. Dosage reduction with each cycle or dose omission within a cycle may be applied based upon the amount of toxicity experienced by the patient.
Gemcitabine in combination with cisplatin has been investigated using two dosage regimens. One regimen used a three week schedule and the other used a four week schedule.
The three week schedule used gemcitabine 1,250 mg/m2, given by 30 minute intravenous infusion, on days 1 and 8 of each 21 day cycle. The three week schedule used cisplatin 75-100 mg/m2 on day 1 of each 21 day cycle, administered before the gemcitabine dose. Dosage reduction with each cycle or dose omission within a cycle may be applied based upon the amount of toxicity experienced by the patient.
The four week schedule used gemcitabine 1,000 mg/m2, given by 30 minute intravenous infusion, on days 1, 8, and 15 of each 28 day cycle. The four week schedule used cisplatin 75-100 mg/m2 on day 1 of each 28 day cycle, administered after the gemcitabine dose. Dosage reduction with each cycle or dose omission within a cycle may be applied based upon the amount of toxicity experienced by the patient.
The recommended dose of gemcitabine is 1,000 mg/m2, given by 30 minute intravenous infusion. This should be repeated once weekly for up to 7 weeks followed by a week of rest. Subsequent cycles should consist of injections once weekly for 3 consecutive weeks out of every 4 weeks. Dosage reduction with each cycle or dose omission within a cycle may be applied based upon the amount of toxicity experienced by the patient.
In patients with bladder cancer who cannot tolerate cisplatin-based combinations, gemcitabine monotherapy should be considered a treatment option.
The recommended dose of gemcitabine is 1,250 mg/m2, given by 30 minute intravenous infusion. The dose should be given on Days 1, 8 and 15 of each 28 day cycle. This four week cycle is then repeated. Dosage reduction with each cycle or dose omission within a cycle may be applied based upon the amount of toxicity experienced by the patient.
The recommended dose for gemcitabine is 1,000 mg/m2, given by 30 minute intravenous infusion. The dose should be given on days 1, 8 and 15 of each 28 day cycle in combination with cisplatin. Cisplatin is given at a recommended dose of 70 mg/m2 on Day 1 following gemcitabine or Day 2 of each 28 day cycle. This four week cycle is then repeated. Dosage reduction with each cycle or dose omission within a cycle may be applied based upon the amount of toxicity experienced by the patient. A clinical trial showed more myelosuppression when cisplatin was used in doses of 100 mg/m2.
Gemcitabine in combination with paclitaxel is recommended using paclitaxel (175 mg/m2) administered on Day 1 over approximately 3 hours as an intravenous infusion, followed by gemcitabine (1250 mg/m2) as a 30-minute intravenous infusion on Days 1 and 8 of each 21 day cycle. Dose reduction with each cycle or within a cycle may be applied based upon the amount of toxicity experienced by the patient.
Gemcitabine in combination with carboplatin is recommended using gemcitabine 1000 mg/m2 administered on Days 1 and 8 of each 21-day cycle as a 30-minute intravenous infusion. After gemcitabine, carboplatin should be given on Day 1 consistent with target AUC of 4.0 mg/mL/min. Dosage reduction with each cycle or within a cycle may be applied based upon the amount of toxicity experienced by the patient.
Patients receiving gemcitabine should be monitored prior to each dose for platelet, leucocyte and granulocyte counts and, if there is evidence of toxicity, the dose of gemcitabine should be reduced or withheld.
Patients receiving gemcitabine should have an absolute granulocyte count of at least 1.5(x109/L) and a platelet count of ³100(x109/L) prior to initiation of a cycle. Dose modifications of gemcitabine on Day 8 and/or Day 15 for haematological toxicity should be performed according to the guidelines below (Tables 1-3).
Gemcitabine Monotherapy or in Combination with Cisplatin
|Absolute Granulocyte Count (x109/L)||Platelet Count (x109/L)||% of full dose|
|> 1.0||and||> 100||100|
|0.5 - 1.0||or||50 - 100||75|
|< 0.5||or||< 50||Hold⚹|
⚹Treatment may be reinstated on Day 1 of the next cycle.
Gemcitabine in Combination with Paclitaxel
|Absolute Granulocyte Count (x109/L)||Platelet Count (x109/L)||% of Day 1 Gemcitabine Dose|
|≥ 1.2||and||> 75||100|
|1.0 - < 1.2||or||50 - 75||75|
|0.7 - < 1.0||and||≥ 50||50|
⚹Treatment may be reinstated on Day 1 of the next cycle.
Gemcitabine in Combination with Carboplatin
|Absolute Granulocyte Count (x109/L)||Platelet Count (x109/L)||% of Day 1 Gemcitabine Dose|
|≥ 1.5||and||≥ 100||100|
|1.0 - < 1.5||or||75-99||50|
⚹Treatment may be reinstated on Day 1 of the next cycle.
Periodic physical examination and checks of liver and kidney function should be made to detect non-haematological toxicity. Dosage reduction with each cycle or dose omission within a cycle may be applied based upon the amount of toxicity experienced by the patient. Doses should be withheld until toxicity has resolved in the opinion of the physician.
Gemcitabine is well tolerated during the infusion, with only a few cases of injection site reaction reported. There have been no reports of injection site necrosis. Gemcitabine can be easily administered on an outpatient basis.
Gemcitabine has been well tolerated in patients over the age of 65. There is no evidence to suggest that dose adjustments are necessary in the elderly, although gemcitabine clearance and half-life are affected by age.
Hepatic and Renal Impairment
Gemcitabine should be used with caution in patients with hepatic insufficiency or with impaired renal function as there is insufficient information from clinical studies to allow clear dose recommendation for this patient population. Dose reduction is recommended in patients with elevated serum bilirubin concentration because such patients are at increased risk of toxicity. In a study of cancer patients with elevated serum bilirubin concentrations1 (median 50 mmol/L, range 30-100 mmol/L) who were administered gemcitabine monotherapy, 8 out of 10 patients experienced toxicity at a gemcitabine dose of 950 mg/m2 compared with 3 out of 8 at 800 mg/m2. The toxicity was mostly related to the liver.
1 Venook AP et al. Phase I and Pharmacokinetic Trial of Gemcitabine in Patients with Hepatic or Renal Dysfunction: cancer and Leukemia Group B 9565, J Clin Oncol 2000, 18: 2780-2787.
In the same study, patients with elevated serum creatinine concentration appeared to experience increased sensitivity to gemcitabine. However, the data based on 15 patients was not sufficient to make dosing recommendations.
All combination studies involving gemcitabine and cisplatin have been performed in patients with creatinine clearance >60 mL/min. There are no safety or pharmacokinetic data available for this combination in patients with creatinine clearance <60 mL/min.
Gemcitabine has been studied in limited Phase 1 and 2 trials in children in a variety of tumour types. These studies did not provide sufficient data to establish the efficacy and safety of gemcitabine in children.
Instructions For Use/Handling
The only approved diluent for reconstitution of gemcitabine sterile powder is 0.9% Sodium Chloride Injection without preservatives. No incompatibilities have been identified, however, it is not recommended to mix gemcitabine with other drugs when reconstituted. Due to solubility considerations, the maximum concentration for gemcitabine upon reconstitution is 40 mg/mL. Reconstitution at concentrations greater than 40 mg/mL may result in incomplete dissolution and should be avoided.
To reconstitute, add 5 mL of 0.9% Sodium Chloride Injection to the 200 mg vial or 25 mL of 0.9% Sodium Chloride Injection to the 1 g vial. Shake to dissolve. These dilutions each yield a gemcitabine concentration of 38 mg/mL, which includes accounting for the displacement volume of the lyophilised powder (0.26 mL for the 200 mg vial or 1.3 mL for the 1 g vial). The total volume upon reconstitution will be 5.26 or 26.3 mL, respectively. Complete withdrawal of the vial contents will provide 200 mg or 1 g of gemcitabine, respectively. The appropriate amount of drug may be administered as prepared or further diluted with 0.9% Sodium Chloride Injection.
Unopened vials should be stored at room temperature. Solutions of reconstituted gemcitabine should be stored at room temperature (15° to 30°C) and in order to reduce possible microbial contamination hazards should be administered within 24 hours. Discard unused portion. Solutions of reconstituted gemcitabine should not be refrigerated, as crystallisation may occur.
Parenteral drugs should be inspected visually for particulate matter and discolouration, prior to administration, whenever solution and container permit. Solutions showing evidence of particulate matter and/or discolouration should not be used.
Procedure for proper handling and disposal of anti-cancer drugs should be considered.
There is no antidote for overdosage of gemcitabine. Single doses as high as 5.7 g/m2 have been administered by IV infusion over 30 minutes every two weeks with clinically acceptable toxicity. In the event of suspected overdose, the patient should be monitored with appropriate blood counts and should receive supportive therapy, as necessary.
GEMZAR is presented in glass vials containing sterile lyophilised powder for reconstitution.
GEMZAR 200 mg, equivalent to 200 mg gemcitabine, is available in 10 mL glass vials with butyl rubber stoppers.
GEMZAR 1 g, equivalent to 1 g gemcitabine, is available in 50 mL glass vials with butyl rubber stoppers.
ELI LILLY AUSTRALIA PTY LIMITED
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