TY - JOUR
T1 - Responses to second-line cisplatin-based intraperitoneal therapy in ovarian cancer
T2 - Influence of a prior response to intravenous cisplatin
AU - Markman, Maurie
AU - Reichman, Bonnie
AU - Hakes, Thomas
AU - Jones, Walter
AU - Lewis, John L.
AU - Rubin, Stephen
AU - Almadrones, Lois
AU - Hoskins, William
PY - 1991/10
Y1 - 1991/10
N2 - Phase II trials of second-line intraperitoneal (IP) cisplatin-based therapy in patients with ovarian cancer have demonstrated the ability of this approach to produce objective antitumor responses, including surgically defined complete responses (CRs), in individuals with persistent small-volume disease after front-line cisplatin-based intravenous (IV) treatment. To examine the influence of a prior response to systemic cisplatin on the activity of second-line IP cisplatin, we retrospectively analyzed two phase II trials of cisplatin-based IP therapy in persistent/recurrent ovarian cancer conducted at our institution. Of the 89 assessable patients on the two trials, 52 (58%) had previously responded to IV cisplatin. The overall response and CR rates to second-line IP cisplatin-based therapy in this previously responding population were 56% and 33%, respectively, compared with overall response and CR rates in the 37 nonresponders to IV cisplatin of 11% and 3%, respectively (P < .001; χ2, 1 df). In the 36 patients responding to systemic cisplatin and whose largest tumor mass measured less than 1 cm at IP cisplatin initiation, a 42% CR rate was observed, compared with a 7% CR rate in the 14 patients with the same bulk of disease who had previously failed to respond to systemic cisplatin (P < .025). We conclude that a prior response to systemic cisplatin strongly influences the antineoplastic activity of second-line IP cisplatin in ovarian cancer.
AB - Phase II trials of second-line intraperitoneal (IP) cisplatin-based therapy in patients with ovarian cancer have demonstrated the ability of this approach to produce objective antitumor responses, including surgically defined complete responses (CRs), in individuals with persistent small-volume disease after front-line cisplatin-based intravenous (IV) treatment. To examine the influence of a prior response to systemic cisplatin on the activity of second-line IP cisplatin, we retrospectively analyzed two phase II trials of cisplatin-based IP therapy in persistent/recurrent ovarian cancer conducted at our institution. Of the 89 assessable patients on the two trials, 52 (58%) had previously responded to IV cisplatin. The overall response and CR rates to second-line IP cisplatin-based therapy in this previously responding population were 56% and 33%, respectively, compared with overall response and CR rates in the 37 nonresponders to IV cisplatin of 11% and 3%, respectively (P < .001; χ2, 1 df). In the 36 patients responding to systemic cisplatin and whose largest tumor mass measured less than 1 cm at IP cisplatin initiation, a 42% CR rate was observed, compared with a 7% CR rate in the 14 patients with the same bulk of disease who had previously failed to respond to systemic cisplatin (P < .025). We conclude that a prior response to systemic cisplatin strongly influences the antineoplastic activity of second-line IP cisplatin in ovarian cancer.
KW - Antineoplastic Combined Chemotherapy Protocols/therapeutic use
KW - Cisplatin/administration & dosage
KW - Cytarabine/administration & dosage
KW - Drug Evaluation
KW - Etoposide/administration & dosage
KW - Female
KW - Humans
KW - Infusions, Intravenous
KW - Infusions, Parenteral
KW - Neoplasm Recurrence, Local/drug therapy
KW - Ovarian Neoplasms/drug therapy
KW - Retrospective Studies
UR - http://www.scopus.com/inward/record.url?scp=0026018186&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:A1991GH45600013&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.1200/JCO.1991.9.10.1801
DO - 10.1200/JCO.1991.9.10.1801
M3 - Article
C2 - 1919630
SN - 0732-183X
VL - 9
SP - 1801
EP - 1805
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 10
ER -