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Marqibo

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Marqibo

Side Effects
Interactions

SIDE EFFECTS

The following adverse reactions are also discussed in other sections of the labeling:

Clinical Trials Safety Experience

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.

Integrated Summary of Safety in Relapsed and/or Refractory Ph- Adult Acute Lymphoblastic Leukemia

Marqibo, at a dose of 2.25 mg/m² weekly, was studied in a total of 83 patients in two trials: study 1 and study 2. Adverse reactions were observed in 100% of patients. The most common adverse reactions ( > 30%) were constipation (57%), nausea (52%), pyrexia (43%), fatigue (41%), peripheral neuropathy (39%), febrile neutropenia (38%), diarrhea (37%), anemia (34%), decreased appetite (33%), and insomnia (32%).

Adverse reactions of Grade 3 or greater were reported in 96% of patients. Adverse reactions of Grade 3 or greater and occurring in ≥ 5% of patients are summarized in Table 2.

Table 2: Most Commonly Reported ( > 5%) Gradea 3 or Greater Adverse Reactions among 83 Patients Receiving the Clinical Dosing Regimen

Adverse Reactions Grade ≥ 3 Study 1 and 2
(N=83)
n (%)
Blood and Lymphatic System Disorders 47 (56.6)
  Febrile Neutropenia 26 (31.3)
  Neutropenia 15 (18.1)
  Anemia 14 (16.9)
  Thrombocytopenia 14 (16.9)
Infections 33 (39.8)
  Pneumonia 7 (8.4)
  Septic Shock 5 (6.0)
  Staphylococcal Bacteremia 5 (6.0)
Neuropathyb 27(32.5)
  Peripheral Sensory and Motor Neuropathy 14 (16.7)
  Constipation 4 (4.8)
  Ileus, Colonic Pseudo-Obstruction 5 (6.0)
  Asthenia 4 (4.8)
  Muscular Weakness 1 (1.2)
Respiratory Thoracic and Mediastinal Disorders 17 (20.5)
  Respiratory Distress 5 (6.0)
  Respiratory Failure 4 (4.8)
General Disorders and Administration Site Condition 31 (37.3)
  Pyrexia 12 (14.5)
  Fatigue 10 (12.0)
  Pain 7 (8.4)
Gastrointestinal Disorders 21 (25.3)
  Abdominal Pain 7 (8.4)
Investigations 20 (24.1)
  Aspartate Aminotransferase Increased 6 (7.2)
Vascular Disorders 8 (9.6)
  Hypotension 5 (6.0)
Psychiatric Disorders 9 (10.8)
  Mental Status Changes 3 (3.6)
Cardiac Disorders 9 (10.8)
  Cardiac Arrest 5 (6.0)
Renal and Urinary Disorders 6 (7.2)
Musculoskeletal and Connective Tissue Disorders 7 (8.4)
a National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v3.0.
bIncluding neuropathy-associated adverse reactions.

A total of 75.9% of patients experienced serious adverse events (SAEs) during the studies. The most commonly reported SAEs included febrile neutropenia (20.5%), pyrexia (13.3%), hypotension (7.2%), respiratory distress (6.0%), and cardiac arrest (6.0%).

Dose reduction, delay, or omission occurred in 53% of patients during the treatment.

Twenty-eight percent of patients experienced adverse reactions leading to treatment discontinuation. The most common adverse reactions that caused treatment discontinuation were peripheral neuropathy (10%), leukemia-related (7%), and tumor lysis syndrome (2%).

Adverse reactions related to neuropathy and leading to treatment discontinuation were decreased vibratory sense, facial palsy, hyporeflexia, constipation, asthenia, fatigue, and musculoskeletal pain, each reported in at least 1 patient.

Deaths occurred in 23% of patients in study 1. The non-leukemia related causes of deaths were brain infarct (1), intracerebral hemorrhage (2), liver failure (1), multi system organ failure (2), pneumonia and septic shock (3), respiratory failure (4), pulmonary hemorrhage (1), and sudden cardiac death (1).

Read the Marqibo (vincristine sulfate liposome injection) Side Effects Center for a complete guide to possible side effects

DRUG INTERACTIONS

No formal drug interaction studies have been conducted with Marqibo. Marqibo is expected to interact with drugs known to interact with non-liposomal vincristine sulfate.

Simultaneous oral or intravenous administration of phenytoin and antineoplastic chemotherapy combinations that included non-liposomal vincristine sulfate have been reported to reduce blood levels of phenytoin and to increase seizure activity.

CYP3A Interactions

Vincristine sulfate, the active agent in Marqibo, is a substrate for cytochrome P450 3A isozymes (CYP3A); therefore, the concomitant use of strong CYP3A inhibitors should be avoided (e.g., ketoconazole, itraconazole, voriconazole, posaconazole, clarithromycin, atazanavir, indinavir, nefazodone, nelfinavir, ritonavir, saquinavir, telithromycin). Similarly, the concomitant use of strong CYP3A inducers should be avoided (e.g., dexamethasone, phenytoin, carbamazepine, rifampin, rifabutin, rifapentine, phenobarbital, St. John's Wort).

P-glycoprotein Interactions

Vincristine sulfate, the active agent in Marqibo, is also a substrate for P-glycoprotein (P-gp). The effect of concomitant use of potent P-gp inhibitors or inducers has not been investigated; it is likely that these agents will alter the pharmacokinetics or pharmacodynamics of Marqibo. Therefore the concomitant use of potent P-gp inhibitors or inducers should be avoided.

Last reviewed on RxList: 8/17/2012
This monograph has been modified to include the generic and brand name in many instances.

Side Effects
Interactions
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