Study study type PathologyT1T0Patientssample sizesROB Results

ovarian cancer (OC) ovarian cancer (OC)

versus bevacizumab plus carboplatin and paclitaxel
atezolizumab plus bevacizumab plus carboplatin plus paclitaxel
AGO-OVAR 2.29/ENGOT-ov34, 2024
  NCT03353831
RCTovarian cancer (OC)atezolizumabSocrecurrent ovarian, fallopian tube, or primary peritoneal cancer with 1st or 2nd relapse within 6 months after completing platinum-based chemotherapy or 3rd relapse285 / 289NA
inconclusive
  • inconclusive 17 % decrease in deaths (OS) (PE)
  • inconclusive 13 % decrease in progression or deaths (PFS) (PE)

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

versus bevacizumab plus carboplatin and paclitaxel
atezolizumab plus bevacizumab plus carboplatin plus paclitaxel
AGO-OVAR 2.29/ENGOT-ov34, 2024
  NCT03353831
RCTovarian cancer (OC)atezolizumabSocrecurrent ovarian, fallopian tube, or primary peritoneal cancer with 1st or 2nd relapse within 6 months after completing platinum-based chemotherapy or 3rd relapse285 / 289NA
inconclusive
  • inconclusive 17 % decrease in deaths (OS) (PE)
  • inconclusive 13 % decrease in progression or deaths (PFS) (PE)

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 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)

metastatic/advanced OC (mOC) - maintenance (M) metastatic/advanced OC (mOC) - maintenance (M)

versus rucaparib
nivolumab based treatment
ATHENA-COMBO (GOG-3020/ENGOT-ov45), 2021
  NCT03522246
RCTmetastatic/advanced OC (mOC) - maintenance (M)combination of rucaparib (Rubraca®) andnivolumab as maintenance treatmentrucaparib alonewomen with newly diagnosed ovarian cancer who responded to their first-line chemotherapy.-/-NA
no results
    no results
from press release May 31 2024 : The primary endpoint of investigator-assessed progression-free survival (PFS) comparing the combination of rucaparib and nivolumab with rucaparib monotherapy was not met in the intent-to-treat (ITT) population