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Clinical trial results for
previously untreated advanced liver cancer

For adults with a type of liver cancer called hepatocellular carcinoma that cannot be removed by surgery or has spread

Actor portrayals.

An FDA-approved combination of two immunotherapies that helped people live longer compared to certain targeted therapies

About the clinical trial

In a clinical trial of 668 people with previously untreated advanced liver cancer, 335 people were given OPDIVO + YERVOY and 333 people were given a targeted therapy, either lenvatinib or sorafenib, chosen by the investigator. This is what’s known as investigator’s choice of therapy.

More people given OPDIVO + YERVOY were alive compared to targeted therapies lenvatinib or sorafenib at 3 years

42% of those given OPDIVO® + YERVOY® for untreated advanced HCC survived longer, versus 32% on other therapies.

People given OPDIVO + YERVOY lived longer compared to targeted therapies lenvatinib or sorafenib

At 24 months, half the people given OPDIVO® + YERVOY® were alive.
OPDIVO + YERVOY

Half the people were alive

At 21 months, half the people given lenvatinib or sorafenib were alive.
Lenvatinib/sorafenib

Half the people were alive

In the primary analysis with a median follow-up of 35 months, people given OPDIVO + YERVOY had a 21% lower risk of dying than those given lenvatinib/sorafenib.

More people given OPDIVO + YERVOY had their tumors shrink or completely disappear compared to targeted therapies lenvatinib or sorafenib

OPDIVO + YERVOY

Lenvatinib/sorafenib

Tumors disappeared completely
(complete response)

7% saw a complete response to OPDIVO® + YERVOY® compared to 2% in response to other therapies for untreated advanced HCC.

Tumors shrank
(partial response)

29% saw a partial response from OPDIVO® + YERVOY® compared to 11% in response to other therapies for untreated advanced HCC.

Tumors shrank or disappeared completely (overall response)

36% given OPDIVO® + YERVOY® saw an overall response compared to 13% given other therapies for untreated advanced HCC.

Half of the people who responded (complete or partial) to OPDIVO + YERVOY continued to respond for at least 30.4 months compared to 12.9 months for people given lenvatinib or sorafenib.

Words to know

Overall response rate is the percentage of patients who responded to treatment. These patients saw their tumors either shrink or disappear completely.

Partial response is when a tumor reacts to treatment and shrinks.

Complete response is when a tumor reacts to treatment and disappears completely. This is the disappearance of any measurable tumors in response to treatment. This does not mean the cancer has been cured.

Duration of response is the measure of how long these responses lasted. The median duration of response is the length of time half of the patients were still responding to treatment.

OPDIVO + YERVOY will not work for everyone. Individual results may vary.

Hands exploring how OPDIVO® (nivolumab) works and learning how this treatment may help fight cancer.

How treatment works

See how this treatment may help your body fight cancer

OPDIVO® (nivolumab) side effects.

Side effects

View side effects of treatment and learn how to manage them

Nurse monitoring a gentleman's infusion of OPDIVO® (nivolumab) immunotherapy treatment.

Getting an infusion

See your recommended treatment plan and what to expect from an infusion

For adults with advanced liver cancer (hepatocellular carcinoma)

OPDIVO® (nivolumab) is a prescription medicine used in combination with YERVOY® (ipilimumab) as a first treatment for adults with a type of liver cancer called hepatocellular carcinoma that cannot be removed by surgery or has spread.

It is not known if OPDIVO is safe and effective in children younger than 12 years of age with melanoma or MSI-H or dMMR metastatic colorectal cancer.

It is not known if OPDIVO is safe and effective in children for the treatment of any other cancers.

OPDIVO (10 mg/mL) and YERVOY (5 mg/mL) are injections for intravenous (IV) use.



7356-US-2500069  04/25