TY - JOUR
T1 - Phase II study of weekly paclitaxel/carboplatin in combination with prophylactic G-CSF in the treatment of gynecologic cancers
T2 - A study in 108 patients by the Belgian Gynaecological Oncology Group
AU - Vergote, Ignace
AU - Debruyne, Philip
AU - Kridelka, Frédéric
AU - Berteloot, Patrick
AU - Amant, Frédéric
AU - Honhon, Brigitte
AU - Lybaert, Willem
AU - Leunen, Karin
AU - Geldhof, Kurt
AU - Verhoeven, Didier
AU - Forget, Frédéric
AU - Vuylsteke, Peter
AU - D'Hondt, Lionel
AU - Huizing, Manon
AU - Van Den Bulck, Heidi
AU - Laenen, Annouschka
N1 - Publisher Copyright:
© 2015 Elsevier Inc. All rights reserved.
PY - 2015/8/1
Y1 - 2015/8/1
N2 - Objective To investigate the addition of prophylactic G-CSF to each weekly paclitaxel/carboplatin course in patients with recurrent platinum-resistant ovarian (OC), or recurrent or advanced endometrial (EC) or cervical carcinoma (CC). Methods 108 patients were enrolled i.e. 36 in each cohort. Eighteen courses of paclitaxel (60 mg/m2) and carboplatin (AUC 2.7) were administered weekly. G-CSF (filgrastim) was given to all patients on day 5 (and if needed on day 6). Results For patients with OC, 91% had platinum-resistant and 9% platinum-refractory disease. Median number of prior chemotherapy lines was 3 for OC, 1 for EC, and 1 for CC. Grade 3-4 neutropenia was observed in 34% of patients (95% CI: 26%-44%, P < 0,0001) (OC 29%, EC 36%, CC 38%). This is lower compared to historical data in all cohorts (84%). Confirmed sepsis was observed in 5%, grade 3-4 thrombocytopenia in 41%, grade 2-3 peripheral neuropathy in 17% of patients. In 71% of patients dose was delayed. Dose reduction was necessary for carboplatin in 47% and paclitaxel in 18% of patients. ORR was 51% (OC 48%, EC 45%, CC 58%). Median (95% CI) PFS and OS was 7.1 (5.1-8.1) and 12.7 (10.2-16.3) months, respectively (OC 7 and 13, EC 6 and 19, CC 6 and 14). Conclusion Weekly paclitaxel/carboplatin with G-CSF is an effective treatment with acceptable toxicity in patients with platinum-resistant or platinum-refractory OC, advanced or recurrent EC and CC. The incidence of grade 3-4 neutropenia is lower with the addition of weekly G-CSF compared with earlier studies without routine use of prophylactic G-CSF.
AB - Objective To investigate the addition of prophylactic G-CSF to each weekly paclitaxel/carboplatin course in patients with recurrent platinum-resistant ovarian (OC), or recurrent or advanced endometrial (EC) or cervical carcinoma (CC). Methods 108 patients were enrolled i.e. 36 in each cohort. Eighteen courses of paclitaxel (60 mg/m2) and carboplatin (AUC 2.7) were administered weekly. G-CSF (filgrastim) was given to all patients on day 5 (and if needed on day 6). Results For patients with OC, 91% had platinum-resistant and 9% platinum-refractory disease. Median number of prior chemotherapy lines was 3 for OC, 1 for EC, and 1 for CC. Grade 3-4 neutropenia was observed in 34% of patients (95% CI: 26%-44%, P < 0,0001) (OC 29%, EC 36%, CC 38%). This is lower compared to historical data in all cohorts (84%). Confirmed sepsis was observed in 5%, grade 3-4 thrombocytopenia in 41%, grade 2-3 peripheral neuropathy in 17% of patients. In 71% of patients dose was delayed. Dose reduction was necessary for carboplatin in 47% and paclitaxel in 18% of patients. ORR was 51% (OC 48%, EC 45%, CC 58%). Median (95% CI) PFS and OS was 7.1 (5.1-8.1) and 12.7 (10.2-16.3) months, respectively (OC 7 and 13, EC 6 and 19, CC 6 and 14). Conclusion Weekly paclitaxel/carboplatin with G-CSF is an effective treatment with acceptable toxicity in patients with platinum-resistant or platinum-refractory OC, advanced or recurrent EC and CC. The incidence of grade 3-4 neutropenia is lower with the addition of weekly G-CSF compared with earlier studies without routine use of prophylactic G-CSF.
KW - Carboplatin
KW - Cervical cancer
KW - Endometrial cancer
KW - G-CSF
KW - Ovarian cancer
KW - Paclitaxel
UR - http://www.scopus.com/inward/record.url?scp=84938213042&partnerID=8YFLogxK
U2 - 10.1016/j.ygyno.2015.05.042
DO - 10.1016/j.ygyno.2015.05.042
M3 - Article
C2 - 26049123
AN - SCOPUS:84938213042
SN - 0090-8258
VL - 138
SP - 278
EP - 284
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 2
ER -