Study study type PathologyT1T0Patientssample sizesROB Results

mOC - L1 - all population metastatic/advanced OC (mOC) - 1st line (L1) mOC - L1 - all population

versus placebo plus SoC
atezolizumab plus SoC
IMagyn-050 (all population), 2021
  NCT03038100
RCTmOC - L1 - all populationatezolizumab plus paclitaxel carboplatin and bevacizumalbplaceb plus paclitaxel carboplatin and bevacizumalbpatients with stage III or stage IV epithelial ovarian, fallopian tube, or primaryperitoneal cancer with either macroscopic residual disease or who will undergo neoadjuvant chemotherapy followed by interval surgery651 / 650low
inconclusive
  • inconclusive 4 % decrease in deaths (OS) (PE)
  • inconclusive 8 % decrease in progression or deaths (PFS) (PE)

mOC - L1 - PDL1 positive metastatic/advanced OC (mOC) - 1st line (L1) mOC - L1 - PDL1 positive

versus placebo plus SoC
atezolizumab plus SoC
IMagyn-050 (PDL1 >1%), 2021
  NCT03038100
RCTmOC - L1 - PDL1 positiveatezolizumab plus paclitaxel carboplatin and bevacizumalbplaceb plus paclitaxel carboplatin and bevacizumalbpatients with stage III or stage IV epithelial ovarian, fallopian tube, or primaryperitoneal cancer with either macroscopic residual disease or who will undergo neoadjuvant therapy followed by interval surgery, PDL1 positive population391 / 393low
suggested
  • inconclusive 2 % decrease in deaths (OS) (PE)
  • suggested 20 % decrease in progression or deaths (PFS) (PE)

metastatic/advanced OC (mOC) - 2nd line (L2) metastatic/advanced OC (mOC) - 2nd line (L2)

versus nivolumab alone
nivolumab plus ipilimumab
NRG GY003, 2020
  NCT02498600
RCTmetastatic/advanced OC (mOC) - 2nd line (L2)nivolumab plus ipilimumabnivolumabpatients with recurrent or persistent ovarian,primary peritoneal, or fallopian tube carcinoma of all histologic types except mucinous adenocarcinoma andcarcinosarcoma with history of primary platinum-basedchemotherapy with a maximum of three prior cytotoxicregimens and with at least one regimen for recurrentdisease containing a platinum or a taxane49 / 51some concern
inconclusive
  • suggested 47 % decrease in progression or deaths (PFS)
  • suggested 2.3-fold increase in objective responses (ORR) (PE)
  • statistically significant 1.3-fold increase in TRAE (grade 3-4)
versus pegylated liposomal doxorubicin
avelumab alone
JAVELIN ovarian 200 (A vs doxorubicin), 2021
  NCT02580058
RCTmetastatic/advanced OC (mOC) - 2nd line (L2)avelumabPegylated liposomal doxorubicinPatients with platinum-resistant/refractory epithelial ovarian, fallopian tube, or peritoneal cancer, unselected for PD-L1 expression (ovarian cancer) a maximum of three previous lines for platinum-sensitive disease (most recent line containing platinum) with no previous systemic therapy for platinum-resistant disease188 / 190some concern
inconclusive
  • inconclusive 14 % increase in deaths (OS) (PE)
  • statistically significant 68 % increase in progression or deaths (PFS) (PE)
avelumab plus pegylated liposomal doxorubicin
JAVELIN ovarian 200 (A/doxorubicin vs doxorubicin), 2021
  NCT02580058
RCTmetastatic/advanced OC (mOC) - 2nd line (L2)avelumab plus PLDPegylated liposomal doxorubicinPatients with platinum-resistant/refractory epithelial ovarian, fallopian tube, or peritoneal cancer, unselected for PD-L1 expression (ovarian cancer) a maximum of three previous lines for platinum-sensitive disease (most recent line containing platinum) with no previous systemic therapy for platinum-resistant disease188 / 190some concern
inconclusive
  • inconclusive 11 % decrease in deaths (OS) (PE)
  • inconclusive 22 % decrease in progression or deaths (PFS) (PE)