Immunotherapy / PD-1 inhibitorFDA-approvedFirst-line

Opdivo

Generic name: nivolumab

How it works

Blocks the PD-1 protein on immune cells, allowing them to recognize and attack cancer cells.

Cancer types

Lung CancerAll patients

Efficacy

Studies show that patients treated with Opdivo had a response rate of approximately 20% and a median overall survival of around 10 months.

Side effects

Moderate

Side effects can be significant and may require dose adjustments or supportive medication, but the treatment is usually continued.

Evidence from research

StudyCancer typeStageEfficacy
Testing Nivolumab and Relatlimab for Melanoma Brain MetastasesMelanomaphase-2Source →
Testing a Combination Treatment for Pancreatic and Lung CancerLung Cancerphase-2Source →
Testing Nivolumab and Hydroxychloroquine for Advanced MelanomaMelanomaphase-1Source →
Pancreatic Cancer Vaccine Trial Evaluates Personalized TreatmentPancreatic Cancerphase-1Source →
Stopping Combo Immunotherapy for Melanoma Brain Metastases May Be SafeMelanomaobservational4-year OS exceeded 83% in patients discontinuing COMBO after CR, PR, or toxicity following CR, compared with 66.4% in those discontinuing due to toxicity after PR.Source →
Evaluating Adaptive Dosing of Immunotherapy for Metastatic MelanomaMelanomaphase-2Source →
Testing Nivolumab for Leptomeningeal DiseaseLung Cancerphase-1Source →
Testing a New Treatment for Advanced MelanomaMelanomaphase-1Source →
Combination Therapy for Untreated Metastatic Pancreatic CancerPancreatic Cancerphase-2Source →
Testing Olanzapine with Nivolumab for Advanced Lung CancerLung Cancerphase-2Source →
Comparing Chemotherapy and Chemo-Immunotherapy for Non-Small Cell Lung CancerLung Cancerphase-3Source →
Testing Immunotherapy with Chemotherapy for Lung CancerLung Cancerphase-2Source →
Testing New Treatments for Advanced Lung CancerLung Cancerphase-2Source →
Testing a New Approach to Treating Advanced MelanomaMelanomapreclinicalSource →
Testing Immunotherapy in Advanced Colorectal CancerColorectal Cancerphase-2Source →
Testing Nivolumab in Rare Solid TumorsBreast Cancerphase-2Source →
New Combination Therapy Tested in Early-Stage Lung CancerLung Cancerphase-1/2The 36-month recurrence-free survival was 80%.Source →
Testing Combination Therapy for Advanced Skin Cancers in Kidney Transplant RecipientsMelanomaphase-1Source →
Melanoma Patient Responds to Repeated Treatment with Ipilimumab and NivolumabMelanomaobservationalSource →
Survival Outcomes After Stopping Nivolumab Due to Side Effects in Lung CancerLung CancerobservationalThe median overall survival was 35.73 months (95% CI: 30.06-41.40).Source →
Testing New Cancer Treatment in Combination with Existing MedicationsLung Cancerphase-1Source →
Rare Sleep Disorder Linked to Cancer TreatmentMelanomaobservationalSource →
Rare Blood Disorder in Lung Cancer Patient Treated with NivolumabLung CancerobservationalSource →
Nivolumab and Ipilimumab Combination Shows Promise in Some Cancer PatientsColorectal Cancerphase-2The disease control rates for breast cancer and other solid tumors were 33% and 32%, respectively.Source →
Testing New Treatments for Advanced MelanomaMelanomaphase-2Source →
Comparing Ways to Give Melanoma MedicationsMelanomaphase-2Source →
Testing Defactinib, Avutometinib, and Nivolumab for Lung CancerLung Cancerphase-2Source →
Testing IL2 and Immunotherapy in Advanced Melanoma PatientsMelanomaphase-2Source →
Testing Nivolumab with Standard Treatment for Colorectal Cancer with BRAF MutationColorectal Cancerphase-2Source →
Evaluating a New Combination Therapy for Advanced Colorectal CancerColorectal Cancerphase-2Source →
COVID-19 Vaccination May Improve Lung Cancer TreatmentLung CancerobservationalPatients receiving ≥2 mRNA doses had significantly longer PFS2 than those receiving 0-1 dose (14.0 vs. 9.6 months; p = 0.04).Source →
Preventing Melanoma Recurrence with NivolumabMelanomaphase-3Source →
Evaluating Nivolumab and Ipilimumab in Combination with Chemotherapy for Lung CancerLung Cancerphase-2Source →
Melanoma Treatment Trial Investigates Combination of NeoVax and ImmunotherapiesMelanomaphase-1Source →
Immunotherapy May Offer Better Survival for Lung Cancer Patients with Poor HealthLung Cancerphase-3Median overall survival was significantly longer with nivolumab: 29-weeks (95% CI: 11.3-46.7) versus 8-weeks (95% CI: 3.5-12.5; p<0.001)Source →
Evaluating Nivolumab and Docetaxel for Advanced Lung CancerLung CancerpreclinicalSource →
Testing Combination Therapy for Advanced Breast Cancer and Solid TumorsBreast Cancerphase-1Source →
Testing New Treatments for Advanced Melanoma That Has ProgressedMelanomaphase-3Source →
Preventing Mucosal Melanoma Return After SurgeryMelanomaphase-2Source →
Testing a New Combination Treatment for Advanced Lung CancerLung Cancerphase-2Source →
Low-dose nivolumab shows promise in treating lung cancerLung Cancerphase-2The estimated 2-year event-free survival rate was 56.1% (95% confidence interval [CI]: 38.3%-73.9%), and the 2-year disease-free survival rate was 66.6% (95% CI: 56.4%-86.8%).Source →
Testing Nivolumab and Ipilimumab with Radiation in Advanced Rectal CancerColorectal Cancerphase-2Source →
Testing Nivolumab to Prevent Leukemia RelapseLeukemiaphase-2Source →
Testing a New Treatment for Advanced Lung CancerLung Cancerphase-1Source →
Trial Tests Cancer Drugs in HIV PatientsBreast Cancerphase-1Source →
Testing Immunotherapy After Surgery for High-Risk MelanomaMelanomaphase-3Source →
Testing Tocilizumab with Immunotherapy for Advanced MelanomaMelanomaphase-2Source →
Immunotherapy Shows Promise for Rare Ovarian and Cervical CancersLeukemiaphase-2The overall response rate was 9.38%, with two complete responses that are ongoing at >3 years and one partial response.Source →
Nivolumab's Safety and Effectiveness in Chinese Lung Cancer PatientsLung CancerobservationalThe median overall survival was 21.2 months.Source →
B cells and genetic changes may predict response to cancer treatmentOvarian Cancerphase-2More than two passenger fusion genes were detected in six of the seven responders, whereas eight of the ten non-responders lacked fusion genes.Source →
GRIm Score Predicts Response to Melanoma TreatmentMelanomaobservationalPatients with a low GRIm Score had significantly longer median progression-free survival (21.4 vs. 6.3 months, p = 0.003) and overall survival (26.5 vs. 7.2 months, p < 0.001).Source →
Combining Immunotherapy for Advanced Anal CancerColorectal Cancerphase-2The median progression-free survival was 2.9 months for nivolumab and 3.7 months for nivolumab plus ipilimumab.Source →
New Biomarker Predicts Outcomes for Lung Cancer Patients on NivolumabLung CancerobservationalPatients with GLR <70.76 achieved significantly longer OS (median 24.1 vs 9.6 months; p < 0.001) and PFS (9.7 vs 5.8 months; p < 0.001) compared with those with GLR ≥70.76.Source →
Rare Side Effect of Cancer Treatment in Older PatientMelanomaobservationalSource →
Fatal Lung Disease after Lung Cancer TreatmentLung CancerobservationalSource →
Combining TM5614 and Nivolumab to Treat Advanced MelanomaMelanomaphase-3Source →
Long-term remission in lung cancer patient treated with nivolumabLung CancerobservationalThe patient remained in continuous remission with a progression-free survival exceeding 82 months and an overall survival exceeding 84 months.Source →
Combination Therapy for Metastatic Melanoma Shows Promise in Real-World StudyMelanomaobservationalThe response rate was 54% (39/72) and, after 13.6 months of median follow-up, a longer median progression-free survival [17.03 months (95% CI 4.8-18.6)].Source →
Immunotherapy Response Predicted by Low Tumor Mutation Burden and PD-L1 ExpressionMelanomaobservationalSource →
Blood Transfusions May Affect Lung Cancer Treatment OutcomesLung CancerobservationalMedian progression-free survival was 5.93 months, and median overall survival was 8.23 months.Source →
Cost-Effectiveness of Lung Cancer Treatment QuestionedLung Cancerphase-3Nivolumab plus bevacizumab and chemotherapy yielded an additional 0.90 QALYs with the marginal cost of $231,948.33.Source →
New Study Explores Using Nivolumab to Treat Malignant AscitesPancreatic Cancerphase-2Seven patients (77.8%) showed a clinical response.Source →
Melanoma Study Examines Vaccine Combination with ImmunotherapyMelanomaphase-2Objective response rates were 59.7% and 59.2% in the two treatment arms.Source →
Combining Nivolumab with Chemotherapy for Advanced Ovarian CancerOvarian Cancerphase-2Fifteen of the 20 evaluable patients had complete gross resection at ICS, and 7 of 20 achieved an optimal pathologic chemotherapy response score of 3.Source →
Immune therapy may trigger severe colitis in some patientsMelanomaobservationalSource →
Combination Treatment Shows Promise for Rare Gynecological CancersOvarian Cancerphase-2The overall objective response rate was 54% (95% CI, 35-71), with 3 (12%) complete responses and 12 (42%) partial responses.Source →
Study Examines Combination Therapy for Advanced Liver CancerColorectal Cancerphase-2Source →
Cost-effectiveness of dual immunotherapy for lung cancerLung Cancerphase-3Nivolumab plus ipilimumab provided an incremental gain of 1.11 and 0.96 QALYs over chemotherapy in the USA and China, respectively.Source →
Comparing Two Ways to Give Cancer TreatmentMelanomaphase-2Source →
Long-term Survival and Response to Immunotherapy in Melanoma PatientsMelanomaphase-2At 4 years from the start of treatment, 80% of patients remained event-free, including 95% of patients who achieved a major pathologic response.Source →
Combining RP1 and Nivolumab May Help Some Melanoma PatientsMelanomaphase-2The confirmed objective response rate was 32.9% (95% CI, 25.2% to 41.3%; 15.0% complete response).Source →
Rare Side Effect of Cancer Treatment: Tongue DiscolorationOvarian CancerobservationalSource →
TIL Therapy for Melanoma Patients May Benefit from IFNα SupportMelanomaphase-2Disease control was obtained in 11.1% of the patients treated without IFNα and in 41.7% of the patients treated with IFNα.Source →
Combination Therapy Improves Survival in Advanced Melanoma PatientsMelanomapreclinicalThe 4-year progression-free survival rate was 30.6% for nivolumab plus relatlimab versus 23.6% for nivolumab alone.Source →
Combination Therapy Shows Promise for Metastatic Uveal MelanomaMelanomaobservationalSource →
Nivolumab Fails to Improve Remission in Acute Myeloid LeukemiaLeukemiaphase-2The median progression-free survival was 13.2 months in the Nivo arm and 10.9 months in the Obs arm.Source →
Color Vision Loss in Melanoma Patient Treated with Nivolumab-RelatlimabMelanomaobservationalSource →
Nivolumab Treatment in Melanoma Patients: Immune and Nutritional Status Linked to SurvivalMelanomaobservationalPatients with high HALP scores had significantly longer progression-free survival (PFS: median 5.8 vs 3.1 months) and overall survival (OS: median 54.9 vs 14.4 months) compared to those with low HALP scores.Source →
Combining Telaglenastat and Nivolumab in Cancer TreatmentMelanomaphase-1/2The overall response rate was 8.4% in the response-assessable analysis set.Source →
Rare Side Effects of Cancer TreatmentMelanomaobservationalSource →
Nivolumab Effectiveness in Non-Small Cell Lung CancerLung CancerobservationalThe 36-month OS rate was 19.7% (95% confidence interval [CI] 17.5-22.0); the 12-month investigator-assessed best ORR in the overall population was 20.4%.Source →
Rare Side Effect of Cancer TreatmentMelanomaobservationalSource →
Brazilian Study Examines Cost of New Melanoma TreatmentsMelanomaobservationalSource →
Inflammatory Markers and Metastases Predict Nivolumab Response in Lung CancerLung CancerobservationalThe median overall survival was 21.2 months (95% CI: 17.4-25.0).Source →
Combination Therapy for Lung Cancer: A Meta-AnalysisLung Cancermeta-analysisNon-small cell lung cancer patients who received combination therapy had better progression-free survival (HR = 0.82, 95% CI 0.71; 0.93, P < 0.01).Source →
Researchers Test New Cancer Treatment in Rare Ovarian CancersOvarian Cancerphase-2The overall response rate was 25% in granulosa cell tumors, with 50% of patients experiencing clinical benefit.Source →
Relatlimab/Nivolumab Combination Therapy for Advanced MelanomaMelanomareviewSource →
Combining Entinostat and Nivolumab in Pancreatic CancerPancreatic Cancerphase-2The objective response rate was 11% (95% CI, 2.4%-29.2%) with a median response duration of 10.2 months.Source →
Long-term Outcomes for Melanoma Patients Treated with Nivolumab and IpilimumabMelanomaphase-3OS was longer with NIVO + IPI versus NIVO monotherapy (hazard ratio, 0.78 [95% CI, 0.67 to 0.91]), with 6-year OS rates of 52% versus 41%, respectively.Source →
Melanoma patients' quality of life during immunotherapy treatmentMelanomaobservationalSource →
Melanoma Patients' Long-Term Survival Rates After TreatmentMelanomaphase-3Estimated cure rates were 48.3% with nivolumab, 38.2% with ipilimumab, and 29.2% with placebo.Source →
Long-term Outcomes with Nivolumab and Ipilimumab in Advanced MelanomaMelanomaphase-3Median overall survival was 71.9 months with nivolumab plus ipilimumab, 36.9 months with nivolumab, and 19.9 months with ipilimumab.Source →
Study Compares Cancer Treatments for Rare Melanoma in Japanese PatientsMelanomaobservationalObjective response rates did not differ significantly between the NIVO+IPI and PD-1 groups (40.0% vs 27.7%).Source →
Researchers Study Effectiveness of Cancer Treatment with Adaptive DosingMelanomaphase-2The overall response rate was 47% (95% CI, 35%-59%) with a median follow-up of 34 months among survivors.Source →
Melanoma Treatment Comparison Study Finds Similar EfficacyMelanomaphase-3Nivolumab plus relatlimab demonstrated similar progression-free survival (hazard ratio, 1.08 [95% CI, 0.88 to 1.33]) and overall survival (HR, 0.94 [95% CI, 0.75 to 1.19]) to nivolumab plus ipilimumab.Source →
Combination Therapy Shows Promise in Lung Cancer TreatmentLung Cancerphase-2The estimated mean 6-month progression-free survival rate was 68.9% (high-MET group) and 50.9% (low-MET group).Source →
Woman's Rare Brain Inflammation Linked to Cancer TreatmentLung CancerobservationalSource →
Nivolumab Monotherapy and Salvage Immunotherapy in Advanced Kidney CancerMelanomaphase-2The 36-month mean time on protocol therapy was 11.5 months, and the 36-month mean TFS for the whole population was 9.4 months.Source →
Nivolumab Shows Promise in Treating Rare CancerLung CancerobservationalThe response rate was 8%, disease control rate was 37%, median progression-free survival was 5.7 months, and median overall survival was 11.1 months.Source →
New Insights into Cancer Treatment for ChildrenMelanomaphase-2Source →
Nivolumab treatment helps patient with advanced melanoma and liver failureMelanomaobservationalSource →
Combining Vaccine and Immunotherapy in Early Prostate CancerProstate Cancerphase-221% of patients had a PSA decline >50%.Source →
Nivolumab Not Cost-Effective for Relapsed Mesothelioma in ChinaLung Cancerphase-3Patients receiving nivolumab gained 0.65 quality-adjusted life-years (QALYs) compared to 0.43 QALYs for those receiving a placebo.Source →
Combining Nivolumab and Chemotherapy in Lung Cancer TreatmentLung Cancerphase-3Median OS was 18.8 months with nivolumab plus chemotherapy versus 15.6 months with chemotherapy in patients with nonsquamous NSCLC.Source →
Immunotherapy Shows Promise for Advanced Colorectal CancerColorectal Cancerphase-2Source →
New Lung Cancer Treatment Combination Shows Mixed ResultsLung Cancerphase-3The clinical benefit rate was 75.5% for sitra + nivo and 64.5% for docetaxel.Source →

This information is provided for general education only and is not medical advice. Always consult a qualified healthcare professional before making treatment decisions.