Phase I study of weekly nedaplatin and concurrent pelvic radiotherapy as adjuvant therapy after radical surgery for cervical cancer

International Journal of Gynecological Cancer

Volumn 18, Issue 5, 2008, Pages 1037-1041

  Kodama, J ^a   Takemoto, M ^a   Seki, N ^a   Nakamura, K ^a   Hongo, A ^a   Kanazawa, S ^a   Hiramatsu, Y ^a  

^a OKAYAMA UNIVERSITY   (Japan)

Author keywords

Cervical cancer; Chemoradiation; Nedaplatin; Phase I study

Indexed keywords

NEDAPLATIN;

ADULT; ANEMIA; ARTICLE; CANCER CHEMOTHERAPY; CANCER RADIOTHERAPY; CANCER STAGING; CLINICAL ARTICLE; CLINICAL TRIAL; CONTROLLED STUDY; CREATININE BLOOD LEVEL; DIARRHEA; DOSE RESPONSE; DRUG DOSE ESCALATION; DRUG EFFICACY; FEMALE; HUMAN; HYSTERECTOMY; LEUKOPENIA; LIVER TOXICITY; LYMPHOCYTOSIS; MULTIPLE CYCLE TREATMENT; NAUSEA; NEUTROPENIA; PHASE 1 CLINICAL TRIAL; PRIORITY JOURNAL; PROCTITIS; PYELONEPHRITIS; SIDE EFFECT; SKIN TOXICITY; THROMBOCYTOPENIA; TREATMENT OUTCOME; UTERINE CERVIX CANCER; VOMITING;

ADULT; ANTINEOPLASTIC AGENTS; DOSE-RESPONSE RELATIONSHIP, DRUG; FEMALE; HUMANS; MIDDLE AGED; NEOPLASM STAGING; ORGANOPLATINUM COMPOUNDS; RADIOTHERAPY, ADJUVANT; TIME FACTORS; UTERINE CERVICAL NEOPLASMS;

EID: 51749083267     PISSN: 1048891X     EISSN: 15251438     Source Type: Journal    
DOI: 10.1111/j.1525-1438.2007.01141.x     Document Type: Article

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