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Chemotherapy, targeted therapy and immunotherapy: Which drugs can be safely used in the solid organ transplant
Umberto Maggiore1,2, Alessandra Palmisano2, Sebastiano Buti3
1Department of Medicine and Surgery, University of Parma, Parma, Italy.
Abstract:
In solid organ transplant recipients, cancer is associated with worse prognosis than in the general population. Among the causes of increased cancer-associated mortality, are the limitations in selecting the optimal anticancer regimen in solid organ transplant recipients, because of the associated risks of graft toxicity and rejection, drug-to-drug interactions, reduced kidney or liver function, and patient frailty and comorbid conditions. The advent of immunotherapy has generated further challenges, mainly because checkpoint inhibitors increase the risk of rejection, which may have life-threatening consequences in recipients of life-saving organs. In general, there are no safe or unsafe anticancer drugs. Rather, the optimal choice of the anticancer regimen results from a careful risk/benefit assessment, from the awareness of potential pharmacokinetic and pharmacodynamic drug-to-drug interactions, and of the risk of drug overexposure in patients with kidney or liver dysfunction. In this review, we summarize general principles that may help the oncologists and transplant physicians in the multidisciplinary management of recipients of solid organ transplantation with cancer who are candidates for chemotherapy, targeted therapy, or immunotherapy.
Insights
Cancer treatment in solid organ transplant recipients is complex due to risks of graft rejection and drug interactions. A careful risk/benefit assessment is crucial for selecting optimal chemotherapy, targeted therapy, or immunotherapy regimens.
Area of Science:
- Oncology
- Transplant Medicine
- Pharmacology
Background:
- Solid organ transplant recipients face a worse cancer prognosis compared to the general population.
- Challenges in cancer treatment include graft toxicity, rejection risk, drug interactions, organ dysfunction, and patient comorbidities.
- Immunotherapy, particularly checkpoint inhibitors, introduces additional risks of life-threatening graft rejection.
Purpose of the Study:
- To provide a review of general principles for managing cancer in solid organ transplant recipients.
- To aid oncologists and transplant physicians in multidisciplinary decision-making for cancer therapy.
- To address the complexities of chemotherapy, targeted therapy, and immunotherapy in this patient population.
Main Methods:
- Review of existing literature and clinical guidelines.
- Analysis of risks and benefits associated with various anticancer treatments.
- Discussion of pharmacokinetic and pharmacodynamic drug interactions.
- Consideration of organ function and patient-specific factors.
Main Results:
- No anticancer drugs are universally safe or unsafe; selection requires individualized risk/benefit assessment.
- Awareness of drug-to-drug interactions and potential for drug overexposure in renal or hepatic dysfunction is critical.
- Checkpoint inhibitors pose a significant risk of graft rejection in transplant recipients.
Conclusions:
- Optimal anticancer regimen selection in solid organ transplant recipients necessitates a thorough risk/benefit evaluation.
- Multidisciplinary collaboration between oncologists and transplant physicians is essential for effective patient management.
- Careful consideration of drug interactions and organ function is paramount for safe and effective cancer treatment.
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