A Phase II Study of Nivolumab + Ipilimumab in Advanced HCC Patients Who Have Progressed on First Line Atezolizumab + Bevacizumab

Inclusion Criteria

• •Age \>= 18 years.
• •HCC diagnosis confirmed by histology/cytology or clinically by American Association for Study of Liver Diseases (AASLD) criteria in cirrhotic patients.
• •Measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) version (v)1.1
• •Locally advanced, metastatic, or unresectable disease.
• •Child Pugh class A.
• •Barcelona clinic liver cancer (BCLC) stage B (not amenable to liver directed therapy) or stage C.
• •Prior treatment with atezolizumab and bevacizumab combination with radiographic progression that necessitates change in treatment per treating physician. Patients with rapid progression on atezolizumab and bevacizumab (defined as patients who progressed radiographically in the first restaging scan that necessitates change in treatment) are excluded.
• •Washout period \>= 4 weeks prior to registration is required since last atezolizumab and bevacizumab dose.
• •Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1. (Form is available on the Academic and Community Cancer Research United \[ACCRU\] website).
• •Absolute neutrophil count (ANC) \>= 1000/mm \^ 3 (obtained =\< 28 days prior to registration).
• •Platelet count \>= 60,000/mm\^3 (obtained =\< 28 days prior to registration).
• •Hemoglobin \>= 8.5 g/dL (obtained =\< 28 days prior to registration).
• •Total bilirubin =\< 3 x upper limit of normal (ULN) (obtained =\< 28 days prior to registration).
• •Alanine aminotransferase (ALT) and aspartate transaminase (AST) =\< 5 x ULN (obtained =\< 28 days prior to registration).
• •International normalized ratio (INR) =\< 2.3 or Prothrombin time (PT) =\< 6 seconds above control OR if patient is receiving anticoagulant therapy and INR is within target range of therapy creatinine =\< 1.5x ULN (obtained =\< 28 days prior to registration).
• •Negative pregnancy test done =\< 7 days prior to registration, for women of childbearing potential only.
• •* Note: If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
• •Provide informed written consent =\< 28 days prior to registration.
• •Willing to return to enrolling institution for follow-up (during the active monitoring phase of the study).
• •* Note: During the active monitoring phase of a study (i.e., active treatment), participants must be willing to return to the consenting institution for follow-up.
• •Willing to provide mandatory tissue specimens and blood specimens for correlative research purposes.
• •Receiving any other investigational agent which would be considered as a treatment for the primary neoplasm =\< 4 weeks prior to registration.
• •Other active malignancy =\< 2 years prior to registration. Exceptions: Non-melanotic skin cancer or carcinoma-in-situ of the cervix.
• •History of myocardial infarction =\< 6 months, or congestive heart failure requiring use of ongoing maintenance therapy for life-threatening ventricular arrhythmias.
• •History of allogenic organ transplantation.
• •Active or prior documented autoimmune or inflammatory disorders (including inflammatory bowel disease \[e.g., colitis or Crohn's disease\], diverticulitis \[with the exception of diverticulosis\], systemic lupus erythematosus, sarcoidosis syndrome, or Wegener syndrome \[granulomatosis with polyangiitis, graves' disease, rheumatoid arthritis, hypophysitis, uveitis, etc\]). The following are exceptions to this criterion:
• •* Patients with vitiligo or alopecia
• •* Patients with hypothyroidism (e.g., following Hashimoto syndrome) stable on hormone replacement
• •* Any chronic skin condition that does not require systemic therapy
• •* Patients without active disease in the last 5 years may be included but only after consultation with the study physician
• •* Patients with celiac disease controlled by diet alone
• •History of leptomeningeal carcinomatosis.
• •Known allergy or hypersensitivity to any of the study drugs or any of the study drug excipients.
• •Current or prior use of immunosuppressive medication =\< 14 days prior to registration. The following are exceptions to this criterion:
• •* Intranasal, inhaled, topical steroids, or local steroid injections (e.g., intra articular injection)
• •* Systemic corticosteroids at physiologic doses not to exceed 10 mg/day of prednisone or its equivalent
• •* Steroids as premedication for hypersensitivity reactions (e.g., computed tomography \[CT\] scan premedication).
• •Receipt of live attenuated vaccine =\< 30 days prior to registration; Note: Patients, if enrolled, should not receive live vaccine whilst on study treatment and up to 30 days after the last dose of study treatment.
• •History of grade 3 or 4 immunotherapy related toxicity NCI CTCAE v5.0 due to prior regimen attributed to atezolizumab.