Histological confirmation of ovarian cancer or tube cancer or primary peritoneal carcinoma stage figo iii
Item
histologically confirmed ovarian cancer or tube cancer or primary peritoneal carcinoma stage figo iii
boolean
C0449575 (UMLS CUI [1,1])
C0029925 (UMLS CUI [1,2])
C0474956 (UMLS CUI [1,3])
C0449575 (UMLS CUI [2,1])
C0153579 (UMLS CUI [2,2])
C0474956 (UMLS CUI [2,3])
C0449575 (UMLS CUI [3,1])
C1514428 (UMLS CUI [3,2])
C0474956 (UMLS CUI [3,3])
primary optimal debulking surgery
Item
primary optimal debulking surgery
boolean
C1708063 (UMLS CUI [1,1])
C1706406 (UMLS CUI [1,2])
postoperative gross residual tumor ≤ 1cm
Item
postoperative gross residual tumor ≤ 1cm ( r0, r1 oder r2 < 1cm situation)
boolean
C0475286 (UMLS CUI [1,1])
C0475440 (UMLS CUI [1,2])
adjuvant chemotherapy with platin and taxane
Item
adjuvant chemotherapy with platin and taxane
boolean
C0085533 (UMLS CUI [1,1])
C3536920 (UMLS CUI [1,2])
C0085533 (UMLS CUI [2,1])
C3541958 (UMLS CUI [2,2])
complete remission after chemotherapy
Item
complete remission after chemotherapy
boolean
C0677874 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
Karnofsky performance score
Item
karnofsky performance score > 60
boolean
C0206065 (UMLS CUI [1])
Age
Item
patients >18 years of age
boolean
C0001779 (UMLS CUI [1])
Written informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
stage figo i or ii
Item
stage figo i or ii
boolean
C0474956 (UMLS CUI [1])
stage iii with postoperative gross residual tumor > 1cm
Item
stage iii with postoperative gross residual tumor > 1cm
boolean
C0474956 (UMLS CUI [1,1])
C0475286 (UMLS CUI [1,2])
stage figo iv
Item
stage figo iv
boolean
C0474956 (UMLS CUI [1])
Recurrence situation
Item
recurrence situation
boolean
C0034897 (UMLS CUI [1])
delayed wound healing post laparotomy
Item
delayed wound healing post laparotomy
boolean
C0151692 (UMLS CUI [1,1])
C0023038 (UMLS CUI [1,2])
Leucopenia <2000/ml before radiotherapy
Item
leucopenia <2000/ml before radiotherapy
boolean
C0023530 (UMLS CUI [1])
Thrombocytopenia <75000/ml before radiotherapy
Item
thrombocytopenia <75000/ml before radiotherapy
boolean
C0040034 (UMLS CUI [1])
clinically active renal, hepatic, cardiac, metabolic, respiratory, coagulation or hematopoietic disease
Item
clinically active renal, hepatic, cardiac, metabolic, respiratory, coagulation or hematopoietic disease
boolean
C0022658 (UMLS CUI [1])
C0023895 (UMLS CUI [2])
C0018799 (UMLS CUI [3])
C0025517 (UMLS CUI [4])
C0035204 (UMLS CUI [5])
C0005779 (UMLS CUI [6])
C1292123 (UMLS CUI [7])
status post pelvic or abdominal radiotherapy
Item
status post pelvic or abdominal radiotherapy
boolean
C0231290 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
C0030797 (UMLS CUI [1,3])
C0231290 (UMLS CUI [2,1])
C1522449 (UMLS CUI [2,2])
C0000726 (UMLS CUI [2,3])
History of other cancer disease in the past 5 years exluding cervical cancer in situ, basal cell carcinoma, squamous cell carcinoma of the skin
Item
status post other cancer disease in the past 5 years (cervical cancer in situ, basal cell carcinoma, squamous cell carcinoma of the skin are excluded)
boolean
C2735087 (UMLS CUI [1])
C2828389 (UMLS CUI [2,1])
C0851140 (UMLS CUI [2,2])
C2828389 (UMLS CUI [3,1])
C0007117 (UMLS CUI [3,2])
C2828389 (UMLS CUI [4,1])
C0553723 (UMLS CUI [4,2])
Participation in another clinical trial
Item
participation in another clinical trial
boolean
C2348568 (UMLS CUI [1])