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1.
Acta Oncol ; 57(6): 807-812, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29265948

ABSTRACT

BACKGROUND: Biliary tract cancer (BTC) is an uncommon cancer with an unfavorable prognosis. Since 2010, the standard of care for patients with unresectable BTC is palliative treatment with gemcitabine plus cisplatin, based on the landmark phase III ABC-02 trial. This current study aims to evaluate the efficacy and safety of gemcitabine and cisplatin in patients with unresectable cholangiocarcinoma and gallbladder cancer in daily practice that meet the criteria for the ABC-02 trial in comparison to patients who did not. METHODS: Patients diagnosed with unresectable BTC between 2010 and 2015 with an indication for gemcitabine and cisplatin were included. We divided these patients into three groups: (I) patients who received chemotherapy and met the criteria of the ABC-02 trial, (II) patients who received chemotherapy and did not meet these criteria and (III) patients who had an indication for chemotherapy, but received best supportive care without chemotherapy. Primary outcome was overall survival (OS) and secondary outcome was progression-free survival (PFS). RESULTS: We collected data of 208 patients, of which 138 (66.3%) patients received first line chemotherapy with gemcitabine and cisplatin. Median OS of 69 patients in group I, 63 patients in group II and 65 patients in group III was 9.6 months (95%CI = 6.7-12.5), 9.5 months (95%CI = 7.7-11.3) and 7.6 months (95%CI = 5.0-10.2), respectively. Median PFS was 6.0 months (95%CI = 4.4-7.6) in group I and 5.1 months (95%CI = 3.7-6.5) in group II. Toxicity and number of dose reductions (p = .974) were comparable between the two chemotherapy groups. CONCLUSION: First-line gemcitabine and cisplatin is an effective and safe treatment for patients with unresectable BTC who do not meet the eligibility criteria for the ABC-02 trial. Median OS, PFS and treatment side effects were comparable between the patients who received chemotherapy (group I vs. group II).


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Biliary Tract Neoplasms/drug therapy , Cholangiocarcinoma/drug therapy , Gallbladder Neoplasms/drug therapy , Palliative Care/methods , Adult , Aged , Aged, 80 and over , Biliary Tract Neoplasms/mortality , Cholangiocarcinoma/mortality , Cisplatin/administration & dosage , Cisplatin/adverse effects , Deoxycytidine/administration & dosage , Deoxycytidine/adverse effects , Deoxycytidine/analogs & derivatives , Disease-Free Survival , Female , Gallbladder Neoplasms/mortality , Humans , Kaplan-Meier Estimate , Male , Middle Aged , Treatment Outcome , Gemcitabine
2.
Cancer Invest ; 24(6): 562-6, 2006 Oct.
Article in English | MEDLINE | ID: mdl-16982459

ABSTRACT

Absorption of a physiological dose of ferrous iron was studied in 18 patients with solid malignancy receiving epoetin therapy for mild chemotherapy-associated anemia. The historical control group consisted of 25 iron replete volunteers (iron absorption 20 +/- 11% in males and 26 +/- 13% in females) and 21 patients with uncomplicated iron deficiency (iron absorption 71 +/- 19%). Iron absorption was increased in the majority of the cancer patients (iron absorption 59 +/- 35%). There were no significant differences in iron absorption between cancer patients who were iron replete or iron deficient according to current clinical practice guidelines (iron deficiency: transferrin saturation < 20% and/or serum ferritin < 100 ng/mL). Red cell iron incorporation was not disturbed in the majority (89%) of patients.


Subject(s)
Anemia/drug therapy , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Erythropoietin/therapeutic use , Hematinics/therapeutic use , Intestinal Absorption , Iron/metabolism , Neoplasms/metabolism , Adult , Aged , Anemia/chemically induced , Anemia/metabolism , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Epoetin Alfa , Female , Hemoglobins/metabolism , Humans , Male , Middle Aged , Neoplasms/drug therapy , Organoplatinum Compounds/administration & dosage , Recombinant Proteins
3.
J Neurooncol ; 70(1): 87-90, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15527113

ABSTRACT

Carcinomatous meningitis is extremely rare in cervical cancer. The diagnosis of carcinomatous meningitis is a difficult one when clinical symptoms are limited and radiographic imaging is normal. Demonstration of malignant cells in the cerebrospinal fluid remains the gold standard to establish the diagnosis. For patients without bulky disease who can be treated with radiotherapy, standard treatment for carcinomatous meningitis is chemotherapy, which may be administered intrathecally. Despite the poor prognosis, treatment may result in effective palliation. We describe a 54-year-old patient who was diagnosed with carcinomatous meningitis in the course of metastatic cervical cancer and who responded to administration of intrathecal methotrexate.


Subject(s)
Meningeal Neoplasms/pathology , Uterine Neoplasms/pathology , Antimetabolites, Antineoplastic/therapeutic use , Female , Humans , Meningeal Neoplasms/drug therapy , Methotrexate/therapeutic use , Middle Aged , Uterine Neoplasms/complications
4.
Anticancer Res ; 23(3C): 3093-6, 2003.
Article in English | MEDLINE | ID: mdl-12926168

ABSTRACT

Testicular germ cell tumours are rarely diagnosed in the elderly. In view of the high cure rate of these tumours, even in elderly patients treatment with chemotherapy and/or radiotherapy should be considered. In this report we describe two older patients with metastatic testicular seminoma. Both were treated with chemotherapy with curative intention. Described are the problems related to treatment with chemotherapy in these elderly.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Seminoma/drug therapy , Testicular Neoplasms/drug therapy , Aged , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Humans , Male , Neoplasm Metastasis , Seminoma/pathology , Testicular Neoplasms/pathology
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