Hear insights from your peers on clinical and patient experiences with COSELA

In this section you can listen to your fellow HCPs share their personal opinions and experiences with COSELA. Use the search and filter functions to find a specific topic, or watch all the videos from a particular HCP.

NOTE: All speakers are appearing on behalf of Pharmacosmos Therapeutics Inc. and were compensated.

Sujith Kalmadi, MD
(Phoenix, AZ)
Shares his experience addressing myelosuppressive side effects and considerations when caring for patients.
TAGS:
Martin Dietrich, MD, PhD
(Orlando, FL)
Shares his experience with adopting COSELA, improving patient care, and why patient experiences matter.
TAGS:
Jason Porter, MD
(Memphis, TN)
Shares why COSELA is now a standard of care for his patients with ES-SCLC.
TAGS:
Jason Porter, MD
(Memphis, TN)
Reviews the multilineage data that compelled him to adopt COSELA.
TAGS:
Jason Porter, MD
(Memphis, TN)
Gives patients’ perspectives on how myelosuppression impacts their daily activities and family time.
TAGS:
Jason Porter, MD
(Memphis, TN)
Describes how chemotherapy dose delays can affect patients and staff.
TAGS:
Jason Porter, MD
(Memphis, TN)
Shares how approaches have evolved for ES-SCLC.
TAGS:
Jason Porter, MD
(Memphis, TN)
Offers his view on why proactively protecting bone marrow is important.
TAGS:
Jason Porter, MD
(Memphis, TN)
Describes how chemotherapy dose delays can affect patients and staff.
TAGS:
Monica Tripodi, APRN, MSN, FNP-C, AOCNP
(Mansfield, TX)
Shares the burden myelosuppression places on patients and their loved ones.
TAGS:
Monica Tripodi, APRN, MSN, FNP-C, AOCNP
(Mansfield, TX)
Talks about chemotherapy delays from the patients’ point of view.
TAGS:
Monica Tripodi, APRN, MSN, FNP-C, AOCNP
(Mansfield, TX)
Recounts some of her practice’s early trials of COSELA and why they adopted it.
TAGS:
Monica Tripodi, APRN, MSN, FNP-C, AOCNP
(Mansfield, TX)
Describes the clinical and patient experiences that led to COSELA becoming a standard of care for her practice.
TAGS:
Monica Tripodi, APRN, MSN, FNP-C, AOCNP
(Mansfield, TX)
Describes how her practice incorporated COSELA into their infusion process and order sets.
TAGS:

IMPORTANT SAFETY INFORMATION

CONTRAINDICATION

  • COSELA is contraindicated in patients with a history of serious hypersensitivity reactions to trilaciclib.

To report suspected adverse reactions, contact Pharmacosmos Therapeutics at 1-888-828-0655 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

INDICATION

COSELA is indicated to decrease the incidence of chemotherapy-induced myelosuppression in adult patients when administered prior to a platinum/etoposide-containing regimen or topotecan-containing regimen for extensive-stage small cell lung cancer (ES-SCLC).

IMPORTANT SAFETY INFORMATION

CONTRAINDICATION

  • COSELA is contraindicated in patients with a history of serious hypersensitivity reactions to trilaciclib.

WARNINGS AND PRECAUTIONS

Injection-Site Reactions, Including Phlebitis And Thrombophlebitis

  • COSELA administration can cause injection-site reactions, including phlebitis and thrombophlebitis, which occurred in 56 (21%) of 272 patients receiving COSELA in clinical trials, including Grade 2 (10%) and Grade 3 (0.4%) adverse reactions. Monitor patients for signs and symptoms of injection-site reactions, including infusion-site pain and erythema during infusion. For mild (Grade 1) to moderate (Grade 2) injection-site reactions, flush line/cannula with at least 20 mL of sterile 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP after end of infusion. For severe (Grade 3) or life-threatening (Grade 4) injection-site reactions, stop infusion and permanently discontinue COSELA. Injection-site reactions led to discontinuation of treatment in 3 (1%) of the 272 patients.

Acute Drug Hypersensitivity Reactions

  • COSELA administration can cause acute drug hypersensitivity reactions, which occurred in 16 (6%) of 272 patients receiving COSELA in clinical trials, including Grade 2 reactions (2%). Monitor patients for signs and symptoms of acute drug hypersensitivity reactions. For moderate (Grade 2) acute drug hypersensitivity reactions, stop infusion and hold COSELA until the adverse reaction recovers to Grade ≤1. For severe (Grade 3) or life-threatening (Grade 4) acute drug hypersensitivity reactions, stop infusion and permanently discontinue COSELA.

Interstitial Lung Disease/Pneumonitis

  • Severe, life-threatening, or fatal interstitial lung disease (ILD) and/or pneumonitis can occur in patients treated with cyclin-dependent kinases (CDK)4/6 inhibitors, including COSELA, with which it occurred in 1 (0.4%) of 272 patients receiving COSELA in clinical trials. Monitor patients for pulmonary symptoms of ILD/pneumonitis. For recurrent moderate (Grade 2) ILD/pneumonitis, and severe (Grade 3) or life-threatening (Grade 4) ILD/pneumonitis, permanently discontinue COSELA.

Embryo-Fetal Toxicity

  • Based on its mechanism of action, COSELA can cause fetal harm when administered to a pregnant woman. Females of reproductive potential should use an effective method of contraception during treatment with COSELA and for at least 3 weeks after the final dose.

ADVERSE REACTIONS

  • Serious adverse reactions occurred in 30% of patients receiving COSELA. Serious adverse reactions reported in >3% of patients who received COSELA included respiratory failure, hemorrhage, and thrombosis.
  • Fatal adverse reactions were observed in 5% of patients receiving COSELA. Fatal adverse reactions for patients receiving COSELA included pneumonia (2%), respiratory failure (2%), acute respiratory failure (<1%), hemoptysis (<1%), and cerebrovascular accident (<1%).
  • Permanent discontinuation due to an adverse reaction occurred in 9% of patients who received COSELA. Adverse reactions leading to permanent discontinuation of any study treatment for patients receiving COSELA included pneumonia (2%), asthenia (2%), injection-site reaction, thrombocytopenia, cerebrovascular accident, ischemic stroke, infusion-related reaction, respiratory failure, and myositis (<1% each).
  • Infusion interruptions due to an adverse reaction occurred in 4.1% of patients who received COSELA.
  • The most common adverse reactions (≥10%) were fatigue, hypocalcemia, hypokalemia, hypophosphatemia, aspartate aminotransferase increased, headache, and pneumonia.

DRUG INTERACTIONS

  • COSELA is an inhibitor of OCT2, MATE1, and MATE-2K. Co-administration of COSELA may increase the concentration or net accumulation of OCT2, MATE1, and MATE-2K substrates in the kidney (e.g., dofetilide, dalfampridine, and cisplatin).

To report suspected adverse reactions, contact Pharmacosmos Therapeutics at 1-888-828-0655 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

This information is not comprehensive. Please see the Full Prescribing Information.