TY - JOUR
T1 - Carcinoma of an unknown primary site
T2 - A chemotherapy strategy based on histological differentiation - Results of a prospective study
AU - Saghatchian, M.
AU - Fizazi, K.
AU - Borel, C.
AU - Ducreux, M.
AU - Ruffié, P.
AU - Le Chevalier, T.
AU - Théodore, C.
PY - 2001/6/5
Y1 - 2001/6/5
N2 - Background: To evaluate the efficacy and toxicity of a chemotherapy strategy based on histological differentiation, for patients with carcinoma of unknown primary site. Patients and methods: Forty-eight patients were prospectively included in the trial. Thirty patients with poorly-differentiated carcinoma or poorly-differentiated adenocarcinoma (group A) received a combination of cisplatin and etoposide. Patients with a responsive or stable disease after two cycles received the same regimen plus bleomycin, ifosfamide and G-CSF. Eighteen patients with well- or moderately-differentiated carcinoma (group B) received cisplatin, continuous infusion 5-fluorouracil (5-FU) and α-interferon. Treatment was maintained in case of response or stable disease for up to six cycles. Results: The overall response rate (RR) for the entire group is 43% (95% confidence interval (CI): 35.9% 50.1%): seven CR and five PR in group A (RR = 40%) and six CR and two PR in group B (RR = 44%). Grade 4 leucopenia was observed in 22 (46%) patients and sepsis in 3 (6%). Median survival is 9.4 months (range 5 13.7 months) and 16.1 months (range 11.8 20.3 months),respectively. Conclusions: This chemotherapy strategy is one way to achieve high response rates, particularly for patients with well- or moderately-differentiated adenocarcinoma usually considered poorly chemosensitive.
AB - Background: To evaluate the efficacy and toxicity of a chemotherapy strategy based on histological differentiation, for patients with carcinoma of unknown primary site. Patients and methods: Forty-eight patients were prospectively included in the trial. Thirty patients with poorly-differentiated carcinoma or poorly-differentiated adenocarcinoma (group A) received a combination of cisplatin and etoposide. Patients with a responsive or stable disease after two cycles received the same regimen plus bleomycin, ifosfamide and G-CSF. Eighteen patients with well- or moderately-differentiated carcinoma (group B) received cisplatin, continuous infusion 5-fluorouracil (5-FU) and α-interferon. Treatment was maintained in case of response or stable disease for up to six cycles. Results: The overall response rate (RR) for the entire group is 43% (95% confidence interval (CI): 35.9% 50.1%): seven CR and five PR in group A (RR = 40%) and six CR and two PR in group B (RR = 44%). Grade 4 leucopenia was observed in 22 (46%) patients and sepsis in 3 (6%). Median survival is 9.4 months (range 5 13.7 months) and 16.1 months (range 11.8 20.3 months),respectively. Conclusions: This chemotherapy strategy is one way to achieve high response rates, particularly for patients with well- or moderately-differentiated adenocarcinoma usually considered poorly chemosensitive.
KW - Cisplatin
KW - Continous infusion 5-FU
KW - Etoposide
KW - Histological differentiation
KW - Unknown primary carcinoma
UR - http://www.scopus.com/inward/record.url?scp=0035007859&partnerID=8YFLogxK
U2 - 10.1023/A:1011129429499
DO - 10.1023/A:1011129429499
M3 - Article
C2 - 11398889
AN - SCOPUS:0035007859
SN - 0923-7534
VL - 12
SP - 535
EP - 540
JO - Annals of Oncology
JF - Annals of Oncology
IS - 4
ER -