Cisplatin

Quick links to important sections

Cisplatin

Selected form

Medically reviewed

Marina Burgos

Last updated on 10/01/2026

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Cisplatin

What is Cisplatin?

Cisplatin is a chemotherapy medication used in the treatment of various types of cancer. It belongs to a group of medicines known as platinum-based antineoplastic agents. Since its discovery and subsequent approval for medical use, it has become a foundational element in oncology for managing solid tumors.

Mechanism of Action

Cisplatin works by interfering with the DNA replication process within cells. When the medication enters the body, it interacts with the DNA inside rapidly dividing cells, creating cross-links. These cross-links prevent the DNA strands from uncoiling and replicating properly. Because cancer cells typically divide faster than healthy cells, they are more susceptible to this interference. When the cell can no longer repair its DNA or replicate, it undergoes a process of programmed cell death.

Clinical Applications

Cisplatin is utilized in the treatment of several different malignancies. It is frequently used as a primary treatment or in combination with other chemotherapy drugs to improve outcomes. Common applications include:

  • Testicular Cancer: It is a core component of curative regimens for germ cell tumors.
  • Ovarian Cancer: It is used to treat advanced or recurrent epithelial ovarian cancer.
  • Bladder Cancer: It is applied in the management of advanced bladder malignancies.
  • Head and Neck Cancers: It is often used alongside radiation therapy for squamous cell carcinomas.
  • Lung Cancer: It is utilized in the treatment of both small cell and non-small cell lung cancer.

History and Development

The properties of cisplatin were first identified in the 1960s during laboratory experiments involving the effects of electric fields on bacterial growth. Researchers observed that platinum electrodes inhibited cell division, leading to the identification of cisplatin as the active compound. This discovery shifted the focus of platinum research toward oncology, eventually establishing cisplatin as one of the most widely used metal-based medications in modern medicine.

Regulatory References

  1. Cisplatin Injection - FDA DailyMed

What side effects are possible with Cisplatin?

Cisplatin’s official safety profile is defined by several well-documented, cumulative, and dose-dependent toxicities, as categorized in regulatory documents.

Adverse Reaction Classification

Adverse reactions are formally classified by frequency and system-organ class. Major toxicities are documented as Very Common (occurring in ge 1/10 patients) and include severe Nephrotoxicity (kidney impairment), Neurotoxicity (nerve damage, such as peripheral neuropathy), Ototoxicity (hearing loss and tinnitus), Myelosuppression (low blood cell counts), and severe gastrointestinal effects (nausea and vomiting).

Common reactions include infection and fever. These classifications strictly reflect official regulatory data.


Serious Reactions and Safety Constraints

The regulatory label highlights several Serious Adverse Reactions, including Acute Renal Failure, severe Anaphylaxis (hypersensitivity), and potentially Irreversible Peripheral Neuropathy. Due to the cumulative nature of these risks, regulatory documents explicitly note that the severity of effects like Nephrotoxicity and Ototoxicity often worsens with repeated courses of treatment.

Population-specific constraints are also outlined. Cisplatin is contraindicated by regulatory authorities in individuals with pre-existing severe renal impairment or hearing impairment. Furthermore, its use is restricted in patients who are dehydrated or have pre-existing myelosuppression, and it is contraindicated during pregnancy due to the risk of fetal harm. These constraints define the medicine's official safety limitations.

Overdose and Emergency Response

The official regulatory profile for Cisplatin overdose focuses on the characteristics of severe, dose-related toxicities. Documented presentations of excessive exposure are marked by severe cumulative nephrotoxicity, potentially leading to acute renal failure, and irreversible peripheral neuropathy. Other manifestations include pronounced and protracted gastrointestinal symptoms (nausea, vomiting, and diarrhoea), as well as significant ototoxicity, which may present as tinnitus and advance to total deafness. Ocular toxicities such as cortical blindness are also documented in severe cases.

Severe outcomes can escalate to life-threatening sepsis due to myelosuppression and the risk of death from severe hypersensitivity reactions (anaphylaxis). Patients must seek immediate medical attention for any suspected overdose or the onset of severe toxicities. Management requires the immediate availability of appropriate diagnostic and treatment facilities. No specific antidote is known. Therefore, treatment is based on general supportive measures, symptomatic treatment, and close monitoring of renal function and serum electrolytes. Regulatory warnings note that ototoxicity may be more pronounced in children and elderly patients may be more susceptible to peripheral neuropathy.

Therapeutic Uses of Cisplatin

Cisplatin is relevant for easing several types of solid tumors and may be part of symptomatic management associated with malignant disease. The central therapeutic action is applied in addressing the tumor burden. This contributes to the overall therapeutic goal of supporting disease control.


Therapeutic Use in Relevant Malignancies

Cisplatin may be part of symptomatic management in therapeutic regimens for specific, relevant malignancies, such as advanced testicular cancer, certain ovarian carcinomas, bladder cancer, and various forms of lung, head and neck, and cervical cancers.

The medication is applied when appropriate for conditions presenting with systemic or localized discomfort, including any existing metastatic spread. This supports the patient during difficult episodes by easing distress and is relevant in addressing disease progression and the overall symptom load.


Functional Role in Combination and Radiation Therapy

Cisplatin is commonly used because its functional ability may assist with other treatments. It is often integrated into combination chemotherapy protocols and used as a radiosensitizer, where its presence may assist in making the malignant cells more susceptible to the effects of concurrent radiation therapy. This strategic use may assist with achieving therapeutic goals, supporting a more focused approach to addressing the malignant process.


Quick Fact: Primary Clinical Goal
Goal Supporting Disease Control, Tumor Reduction
Benefit Supports the patient by easing the overall symptom load
Scenario Treatment of advanced, aggressive, or recurrent solid tumors

Regulatory References

  1. National Cancer Institute (NCI)

Eligibility and Restrictions for Use

Eligibility Map: Who can and cannot use Cisplatin — Official Regulatory Information

The eligibility profile for Cisplatin is strictly defined by regulatory documents, outlining populations that are absolutely contraindicated due to risk of severe toxicity.


Absolute Contraindications

Official labeling strictly contraindicates Cisplatin use in patients with:

  • Pre-existing renal impairment (kidney function below specified thresholds).
  • Pre-existing hearing impairment (ototoxicity).
  • Pre-existing myelosuppression (bone marrow depression).
  • A history of severe hypersensitivity to Cisplatin or any platinum-containing compound.
  • Dehydration or when receiving the Yellow Fever Vaccine.

Restricted and Conditional Use

Use is not recommended during pregnancy, and it is contraindicated during lactation (breastfeeding). Females of reproductive potential must use effective contraception during and for a specified time following treatment. Eligibility for repeat courses is strictly conditional on meeting pre-defined laboratory thresholds for renal function and hematologic status. While generally applicable, use in older adults and the pediatric population requires enhanced monitoring due to increased susceptibility to neurotoxicity and nephrotoxicity.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Regulatory documents establish the official interaction profile of Cisplatin through classifications based on additive toxicity, altered clearance, and physical incompatibility. The most critical restriction is the prohibition against using any administration equipment (needles, IV sets, or syringes) containing metallic aluminum, as this causes a black precipitate and a documented loss of drug potency.

Documented Pharmacodynamic Interactions

Co-administration with other nephrotoxic medicinal products, such as Aminoglycoside antibiotics, formally potentiates the Cisplatin-related toxic effect on the kidneys (nephrotoxicity). Similarly, co-administration with ototoxic substances, including Loop Diuretics, formally potentiates the toxic effect on auditory function. This pharmacodynamic potentiation establishes an interaction-related constraint for these drug classes.

Pharmacokinetic and Timing Constraints

Cisplatin is documented to alter the clearance of certain co-administered agents. When administered prior to Paclitaxel, for instance, Cisplatin increases Paclitaxel exposure due to reduced renal clearance. Conversely, Cisplatin is documented to reduce the levels of Magnesium Oxide by increasing its renal clearance. Additionally, regulatory guidance states that forced diuresis using Loop Diuretics is not advised in certain patients due to heightened risk of cumulative toxicity. Furthermore, Geriatric patients may exhibit increased susceptibility to Cisplatin-related organ toxicity, which heightens the relevance of interactions with nephrotoxic agents.

Mechanism of Action

Covalent Binding to DNA and Helix Distortion

The mechanism begins inside the cell where Cisplatin transforms into a highly reactive platinum complex through a process called aquation, specifically targeting the nuclear DNA. This complex forms strong, irreversible covalent bonds with the DNA strands, primarily creating bulky intrastrand cross-links on adjacent guanine bases. This molecular action physically distorts the DNA helix, which is a critical step that commits the cell to the cytotoxic cascade.


Blockade of Replication and Apoptotic Trigger

The physical distortion caused by the platinum adducts acts as a roadblock, effectively halting DNA replication and RNA transcription, which are essential processes for cellular maintenance and proliferation. When the cell's repair mechanisms are overwhelmed by this irreparable damage, a protective cascade known as the DNA Damage Response (DDR) pathway is activated. This response ultimately triggers Apoptosis (programmed cell death), resulting in the controlled cellular elimination of the damaged cells.


Mechanism Limitations: Resistance Factors

The intended cytotoxic effect may be limited by cellular resistance mechanisms. This occurs when target cells either successfully reduce drug entry (e.g., via altered transporter expression), increase drug deactivation (e.g., binding the platinum complex to Glutathione), or enhance their capacity for DNA repair. These biological activities can functionally reverse the drug's mechanism, allowing the cell to bypass the programmed death cascade.

Dosage and Administration Information

How to use Cisplatin

The administration of Cisplatin is governed by strict protocols outlined in clinical documentation, ensuring its use in a specialized setting. The medicine is supplied as a concentrate for solution for infusion and must be administered exclusively via slow intravenous (IV) infusion.

Dosing and Schedule

Cisplatin is used in intermittent, cyclical regimens, typically administered every three to four weeks. The exact dose is determined by body surface area, expressed in milligrams per square meter (mg/m²). Standard single-dose regimens for monotherapy range from 50 to 120 mg/m^2 per cycle; alternatively, a multi-day regimen of 15 to 20 mg/m^2 daily for five consecutive days may be used. Repeat courses of treatment are strictly conditional upon the patient meeting acceptable blood count and renal function parameters.

Administration Requirements

Due to its nature, Cisplatin administration requires several mandatory procedural steps:

  1. Preparation and Dilution: The concentrate must be diluted in approved vehicles, such as 0.9% sodium chloride solution, prior to infusion. Crucially, the solution must not come into contact with aluminum components, as this causes a chemical reaction that can precipitate the drug and reduce its potency.
  2. Infusion Rate: The infusion must be administered slowly, generally over a period of 6 to 8 hours, and rapid IV injection is prohibited.
  3. Mandatory Hydration: Extensive pre- and post-treatment hydration with intravenous fluids is required before and after the infusion, typically over 24 hours, to maintain fluid balance as specified in the administration protocol.

These clinical instructions collectively define a precise, controlled administration protocol that must be followed in a specialized environment.

Recent Clinical Evidence

Cisplatin is a chemotherapy agent that has been a long-standing component of treatment regimens for several types of cancer. Recent clinical and non-clinical research continues to examine its use, particularly in combination with newer agents and radiation therapy, and focuses on optimizing its administration.

Core Indications and Combination Regimens

Cisplatin is commonly used in treatment protocols for advanced cancers, including:

  • Testicular Cancer: It remains a critical component of first-line therapy.
  • Ovarian Cancer: Often administered in combination with other chemotherapy drugs.
  • Bladder Cancer: Used for locally advanced or metastatic cases.
  • Head and Neck Cancer (SCCHN): Frequently employed as a radiosensitizer alongside radiation therapy.

Recent Research Focus

Clinical investigations are largely directed at managing and mitigating the drug's known adverse effects, which is crucial for improving treatment completion rates and long-term quality of life. Key areas of study include:

Area of Research Finding or Goal
Toxicity Mitigation Studies focus on optimized hydration and prophylactic agents to reduce nephrotoxicity (kidney damage) and ototoxicity (hearing loss).
Combined Therapy Research explores combining cisplatin with agents like PARP inhibitors to potentially re-sensitize resistant cancer cells.
Long-Term Effects Ongoing observational studies track the long-term impact on survivors, particularly concerning hearing function and peripheral neuropathy.

Standardized guidance for the administration of cisplatin during chemoradiation, informed by clinical trial protocols and retrospective data, aims to reduce toxicity and minimize treatment delays, ensuring consistent care.

Frequently Asked Questions (FAQ)

Common questions about Cisplatin (FAQ)


Q: Does Cisplatin cause hair loss in everyone?

A: Hair loss, or alopecia, is listed in official product information as a possible adverse effect. However, data indicates that it does not occur in every patient receiving the medicine. The degree of severity can vary, and hair loss is sometimes described as temporary.


Q: Do older people react differently to Cisplatin treatment?

A: Regulatory documents indicate that older adults (geriatric patients) may have an increased susceptibility to toxic effects, such as nerve damage (neurotoxicity) and kidney damage (nephrotoxicity). Due to this potential for heightened risk, enhanced monitoring of these organ systems is often required for this population.


Q: How quickly do the side effects of Cisplatin usually start?

A: The onset of side effects varies widely depending on the type of reaction. For example, severe nausea and vomiting may begin shortly after administration. In contrast, other effects like nerve damage or kidney impairment are often cumulative and may worsen over repeated courses of treatment rather than starting immediately.


Q: Do all side effects of Cisplatin go away after the treatment stops?

A: No, not all side effects are guaranteed to resolve. The regulatory label describes certain effects, particularly peripheral neuropathy (nerve damage), as being potentially irreversible. The severity of effects like hearing loss (ototoxicity) often also worsens with repeated courses and may persist after the treatment concludes.


Q: Is it necessary to stay in the hospital for Cisplatin infusion?

A: Cisplatin must be administered in a specialized clinical environment. The treatment involves a slow intravenous (IV) infusion that typically lasts several hours, and it requires mandatory pre- and post-treatment IV hydration. These necessary safety and procedural steps mean that the infusion and monitoring commonly require an extended stay in a clinical setting.


Q: Is there ongoing research into new uses or improved versions of Cisplatin?

A: Research into Cisplatin is ongoing, according to information from major cancer institutes. This research is primarily focused on strategies for toxicity mitigation—such as reducing kidney damage and hearing loss—and exploring its use in combined therapy with newer medicines to potentially overcome resistance.


Q: Can Cisplatin be used to treat types of cancer other than those listed in official documents?

A: This FAQ section focuses exclusively on the uses that are officially cleared by regulatory agencies. Regulatory documents list the approved uses for Cisplatin, which include advanced testicular, ovarian, and bladder cancers, among others.


Q: How long does the effect of Cisplatin last after a treatment session?

A: Cisplatin is typically administered in intermittent, cyclical regimens, often repeated every three to four weeks. While the drug is quickly cleared from the plasma, its therapeutic action involves causing irreversible DNA damage to cancer cells, a cellular effect that persists after the infusion is complete.


Q: Is it true that Cisplatin can affect hearing?

A: Yes. Official warnings indicate that Cisplatin can cause ototoxicity, which means damage to the ear resulting in symptoms like hearing loss and tinnitus (ringing in the ears). Ototoxicity is listed as a very common adverse reaction and is a factor considered when determining eligibility for the medicine.


Q: What is the difference between Cisplatin and Carboplatin?

A: Cisplatin and Carboplatin are both platinum-based chemotherapy agents. Carboplatin is classified as an analogue of Cisplatin, meaning it is similar in structure. Regulatory descriptions indicate they have distinct characteristics, particularly in their toxicity profiles, which influences their respective uses in treatment protocols.


Q: Are there specific food types to avoid during Cisplatin therapy?

A: Official regulatory documents typically do not list specific food types to avoid due to formal drug-food interactions. However, patients are often medically managed for severe nausea and vomiting, and dietary modifications are commonly advised to help manage these gastrointestinal side effects.


Q: Is feeling extreme fatigue normal after a Cisplatin infusion?

A: Yes, regulatory documents list fatigue and asthenia (physical weakness or lack of energy) as a very common adverse reaction. This lack of energy is frequently reported by patients undergoing treatment with Cisplatin.


Q: Does Cisplatin affect fertility in men and women?

A: Official warnings address the potential for Cisplatin to affect fertility. Patients are advised to discuss the risk of temporary or permanent sterility with their healthcare team. Official warnings state that females of reproductive potential are advised to use effective contraception during and for a specified time following treatment.


Q: What kind of studies support the use of Cisplatin for testicular cancer?

A: Cisplatin's use is supported by a significant body of official clinical evidence. Studies established its role as a critical component of first-line therapy for advanced testicular cancer, which informs its inclusion in official treatment guidelines and protocols.


Q: Can Cisplatin be given to children?

A: Official documentation notes that the use of Cisplatin in the pediatric population requires enhanced monitoring. This is due to the potential for an increased susceptibility to certain toxicities. The suitability and dosage are based on the patient's specific condition and the approved protocol, and require a physician's determination.


Q: Can Cisplatin cause changes in taste or smell?

A: Yes. Adverse reaction listings may include changes in taste, known as dysgeusia. This has been reported in clinical data and can sometimes affect a patient's appetite and food enjoyment during the course of treatment.


Q: What is 'chemobrain' and is it associated with Cisplatin?

A: The term 'chemobrain' (cognitive difficulties) is not generally used in official regulatory documents. However, Cisplatin is formally associated with neurotoxicity (nerve damage). Central nervous system effects, such as dizziness, have also been reported in clinical trial data.


Q: Are there certain heart conditions that mean someone shouldn't use Cisplatin?

A: Absolute contraindications are mainly listed for kidney function, hearing, and severe hypersensitivity. While serious cardiovascular events like hypotension (low blood pressure) can occur acutely during administration, pre-existing heart conditions are not typically listed as absolute contraindications in the same way as kidney or hearing impairment.


Q: Is Cisplatin a new or an older drug?

A: Cisplatin is an older and well-established drug within the therapeutic field of chemotherapy. Its discovery and clinical use date back to the 1970s, making it a foundational and widely used compound.


Q: Can Cisplatin treatment be given at home?

A: No. Official administration guidelines mandate that Cisplatin must be given in a specialized clinical environment. This is due to the complex preparation, the need for a slow IV infusion, and the mandatory requirement for pre- and post-treatment hydration and close monitoring.


Q: What should a patient know about their diet while on Cisplatin?

A: Official documents do not list specific food items to avoid. However, due to the high risk of severe nausea and vomiting, which are common side effects, patients are typically managed with anti-nausea medication, and dietary modifications are often advised to reduce symptoms.


Q: How does Cisplatin affect the body's immune system?

A: Cisplatin commonly causes myelosuppression (bone marrow depression), which is a reduction of certain blood cell counts, including white blood cells. This effect can increase the risk of infection, which is listed as a common adverse reaction in official safety documents.


Q: Is it true that patients are given other medicines to prevent Cisplatin side effects?

A: Yes. Official protocols state that patients should receive adequate antiemetic (anti-nausea) medication before and after Cisplatin administration to help prevent severe nausea and vomiting. Pre-treatment with intravenous hydration is also mandatory to protect the kidneys.


Q: Can Cisplatin be used for non-cancerous conditions?

A: Cisplatin is formally cleared by regulatory authorities for the treatment of malignant (cancerous) conditions only, specifically testicular, ovarian, and bladder cancers, among others. It is not cleared for use in non-cancerous conditions.


Q: Are there specific genetic markers that predict how a patient will respond to Cisplatin?

A: Scientific research has examined the role of genetic variants in influencing a patient's response to Cisplatin and their risk of toxicity. However, these markers are not currently used in the standard regulatory labeling to universally determine eligibility or dosing.


Q: Can Cisplatin cause long-term nerve damage?

A: Yes. The regulatory label describes peripheral neuropathy (nerve damage) as a common, dose-dependent, and sometimes irreversible effect. These effects can potentially persist or worsen following the completion of treatment.


Q: Why are there warnings about Cisplatin and sunlight exposure?

A: Some patients receiving chemotherapy, including Cisplatin, are often cautioned regarding sunlight exposure. This caution is often provided because the skin may become more sensitive to sunlight (photosensitivity) during treatment, which is a common consideration for many cytotoxic agents.


Q: Does Cisplatin affect the liver?

A: Reports of liver enzyme elevations have been noted in clinical data summarized in regulatory sources, indicating that Cisplatin can potentially affect the liver (hepatotoxicity). However, clinically apparent, acute liver injury is considered rare.


Q: Are there specific restrictions on driving or operating machinery while receiving Cisplatin?

A: Official regulatory documents do not provide specific, universal restrictions on driving. However, because Cisplatin can cause adverse effects like fatigue, dizziness, and vision changes, patients are typically cautioned to be aware of the effects when performing skilled tasks or operating machinery.


Q: Can Cisplatin treatment cause low blood pressure?

A: Yes. Hypotension (low blood pressure) may occur acutely during or shortly after Cisplatin administration and is noted in the adverse reactions section of regulatory documents. This is often monitored closely during the infusion period.


Q: What kind of follow-up care is needed after stopping Cisplatin?

A: Post-treatment monitoring is necessary because Cisplatin can cause cumulative, long-term toxicities. Follow-up care often includes continued monitoring of kidney function, hearing (audiometry), and neurological status for a specified period after the treatment ends.


Q: Can I have alcohol while I'm on Cisplatin treatment?

A: Official drug labels typically do not provide explicit rules on alcohol consumption. However, given that Cisplatin can cause severe nausea and vomiting and may affect the liver, alcohol consumption is generally noted as a factor to be managed during therapy, as it can potentially worsen these effects.

How should Cisplatin be stored and disposed of?

Storage and Stability Requirements

The unopened Cisplatin Injection vial must be stored at Controlled Room Temperature, typically 15 C to 25 C. It is mandatory to protect the unopened container from light and it must not be refrigerated or frozen, as cold temperatures may cause the drug to precipitate.

For a multiple-dose vial, the solution remaining after initial entry is stable for up to 28 days when protected from light and stored at 15 C to 25 C. The medicine must be kept out of the sight and reach of children.

Handling and Disposal

Cisplatin is classified as a hazardous cytotoxic agent. During handling and preparation, contact with aluminum-containing devices must be avoided, as this material is incompatible and can cause the drug to lose potency.

Disposal of any unused product, expired medicine, or items contaminated during handling must be carried out according to local regulations for antineoplastic or hazardous waste. The product must not be discarded in household waste or down any drain.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

Available in countries:

Equivalent of Cisplatin found in:

A-Z Index: