TY - JOUR
T1 - Aggressive chemosurgical debulking in patients with advanced ovarian cancer
AU - Ng, Laura W.
AU - Rubin, Stephen C.
AU - Hoskins, William J.
AU - Jones, Walter B.
AU - Hakes, Thomas B.
AU - Markman, Maurie
AU - Reichman, Bonnie
AU - Almadrones, Lois
AU - Lewis, John L.
PY - 1990/9
Y1 - 1990/9
N2 - From July 1986 to June 1989, 43 evaluable patients with advanced ovarian cancer were treated on protocol with initial cytoreductive surgery, two courses of high-intensity intravenous Cytoxan (1000 mg/m2) and cisplatin (120-200 mg/m2) chemotherapy, and repeat debulking laparotomy in an effort to maximize response to a subsequent four cycles of intraperitoneal platinum-based chemotherapy. Two patients were stage IIIA, 2 stage IIIB, 28 stage IIIC, and 11 stage IV. Five tumors were grade 1, 9 grade 2, and 29 grade 3. Thirty-eight (88%) patients had bulky tumor (5-25 cm) found at first laparotomy; 25 of these had >1-cm residual after initial debulking. Following two cycles of intensive intravenous chemotherapy 18 of these 25 had >1-cm disease found at second laparotomy; 12 of 18 underwent secondary cytoreduction to <1 cm. Thus, 30 of these 38 (79%) patients entered the intraperitoneal phase of the protocol with <1-cm disease. Four patients had 2- to 5-cm tumor at initial laparotomy; two of four were debulked to <1-cm residual. All four were found to have <1-cm disease at second laparotomy. This combination regimen was well tolerated. There was one treatment-related death. In sum, 42 of 43 patients had tumor >2 cm at staging laparotomy and 38 (88%) had large, bulky disease (5-25 cm); 34 of 43 (79%) entered the intraperitoneal phase of the protocol with optimal (<1-cm) disease. Aggressive chemosurgical cytoreduction in patients with bulky advanced ovarian cancer can leave a large proportion of patients with minimal residual disease and maximize their chances of responding to subsequent intraperitoneal chemotherapy.
AB - From July 1986 to June 1989, 43 evaluable patients with advanced ovarian cancer were treated on protocol with initial cytoreductive surgery, two courses of high-intensity intravenous Cytoxan (1000 mg/m2) and cisplatin (120-200 mg/m2) chemotherapy, and repeat debulking laparotomy in an effort to maximize response to a subsequent four cycles of intraperitoneal platinum-based chemotherapy. Two patients were stage IIIA, 2 stage IIIB, 28 stage IIIC, and 11 stage IV. Five tumors were grade 1, 9 grade 2, and 29 grade 3. Thirty-eight (88%) patients had bulky tumor (5-25 cm) found at first laparotomy; 25 of these had >1-cm residual after initial debulking. Following two cycles of intensive intravenous chemotherapy 18 of these 25 had >1-cm disease found at second laparotomy; 12 of 18 underwent secondary cytoreduction to <1 cm. Thus, 30 of these 38 (79%) patients entered the intraperitoneal phase of the protocol with <1-cm disease. Four patients had 2- to 5-cm tumor at initial laparotomy; two of four were debulked to <1-cm residual. All four were found to have <1-cm disease at second laparotomy. This combination regimen was well tolerated. There was one treatment-related death. In sum, 42 of 43 patients had tumor >2 cm at staging laparotomy and 38 (88%) had large, bulky disease (5-25 cm); 34 of 43 (79%) entered the intraperitoneal phase of the protocol with optimal (<1-cm) disease. Aggressive chemosurgical cytoreduction in patients with bulky advanced ovarian cancer can leave a large proportion of patients with minimal residual disease and maximize their chances of responding to subsequent intraperitoneal chemotherapy.
KW - Cisplatin/therapeutic use
KW - Combined Modality Therapy
KW - Cyclophosphamide/therapeutic use
KW - Female
KW - Humans
KW - Injections, Intravenous
KW - Ovarian Neoplasms/drug therapy
KW - Prognosis
UR - https://www.scopus.com/pages/publications/0025152104
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:A1990EE33000012&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.1016/0090-8258(90)90073-T
DO - 10.1016/0090-8258(90)90073-T
M3 - Article
C2 - 2227548
SN - 0090-8258
VL - 38
SP - 358
EP - 363
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 3
ER -