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NCT01081262 · OUTCOME

Participants With Grade 1 or Higher Non-serious Adverse Effects Assessed by CTCAE Version 4.0

Carboplatin and Paclitaxel or Oxaliplatin and Capecitabine With or Without Bevacizumab as First-Line Therapy in Treating Patients With Newly Diagnosed Stage II-IV or Recurrent Stage I Epithelial Ovarian or Fallopian Tube Cancer · Source last updated 2026-08-28

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
COUNT_OF_PARTICIPANTS
Unit
Participants
Interval / dispersion
Not reported
Time frame
Every cycle while on treatment, up to 5 years

What was measured

Grade 1 or higher non-serious adverse events were graded by CTC AE v 4.

Analysis population: Eligible and treated patients

Groups in this outcome

Arm I (Carboplatin and Paclitaxel)

Patients receive carboplatin IV over 30-60 minutes on day 1 and paclitaxel IV over 3 hours on day 1. Treatment repeats every 3 weeks for 6 courses in the absence of disease progression or unacceptable toxicity. Carboplatin: Given IV Laboratory Biomarker Analysis: Correlative studies Paclitaxel: Given IV Quality-of-Life Assessment: Ancillary studies

Arm II (Oxaliplatin and Capecitabine)

Patients receive oxaliplatin IV over 2-6 hours on day 1 and capecitabine PO BID on days 1-14. Treatment repeats every 3 weeks for 6 courses in the absence of disease progression or unacceptable toxicity. Capecitabine: Given PO Laboratory Biomarker Analysis: Correlative studies Oxaliplatin: Given IV Quality-of-Life Assessment: Ancillary studies

Arm III (Carboplatin, Paclitaxel, Bevacizumab)

Patients receive carboplatin and paclitaxel IV as in arm I and bevacizumab IV over 30-90 minutes on day 1. Treatment repeats every 3 weeks for 6 courses in the absence of disease progression or unacceptable toxicity. Patients then receive bevacizumab IV over 30-90 minutes alone on day 1. Treatment repeats every 3 weeks for 12 courses in the absence of disease progression or unacceptable toxicity. Bevacizumab: Given IV Carboplatin: Given IV Laboratory Biomarker Analysis: Correlative studies Paclitaxel: Given IV Quality-of-Life Assessment: Ancillary studies

Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)

Patients receive oxaliplatin and capecitabine as in arm II, and bevacizumab as in arm III. Bevacizumab: Given IV Capecitabine: Given PO Laboratory Biomarker Analysis: Correlative studies Oxaliplatin: Given IV Quality-of-Life Assessment: Ancillary studies

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
Arm I (Carboplatin and Paclitaxel)13
Arm II (Oxaliplatin and Capecitabine)13
Arm III (Carboplatin, Paclitaxel, Bevacizumab)13
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)11

Reported measurements

Abnormal lab values
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)8Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)10Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)10Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)10Not reportedNot reportedNot reportedNot reported
Allergic reaction
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)3Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)1Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)4Not reportedNot reportedNot reportedNot reported
Allergic rhinitis
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)0Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)1Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)1Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)1Not reportedNot reportedNot reportedNot reported
Alopecia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)11Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)1Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)9Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)5Not reportedNot reportedNot reportedNot reported
Anemia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)12Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)7Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)4Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)6Not reportedNot reportedNot reportedNot reported
Bleeding
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)1Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)1Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)3Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)5Not reportedNot reportedNot reportedNot reported
Cold-like symptoms
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)2Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)3Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)7Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)6Not reportedNot reportedNot reportedNot reported
Constipation
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)3Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)4Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)7Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)9Not reportedNot reportedNot reportedNot reported
Diarrhea
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)5Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)6Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)5Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)8Not reportedNot reportedNot reportedNot reported
dyspnea
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)2Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)1Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)3Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Edema Limbs
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)0Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)1Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Fatigue
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)10Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)10Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)8Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)11Not reportedNot reportedNot reportedNot reported
Fever
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)3Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)0Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)2Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)1Not reportedNot reportedNot reportedNot reported
Hand/Foot Syndrome
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)1Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)0Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)7Not reportedNot reportedNot reportedNot reported
Headache
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)3Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)4Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)5Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)4Not reportedNot reportedNot reportedNot reported
Hypertension
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)3Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)8Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)9Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)10Not reportedNot reportedNot reportedNot reported
Hypomagnesemia
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)1Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)0Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)2Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Infection
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)4Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)0Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)3Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)3Not reportedNot reportedNot reportedNot reported
Laryngeal Spasm
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)0Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)4Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Low Lymphocytes
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)1Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)1Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)2Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Low Mood
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)1Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)2Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)1Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)1Not reportedNot reportedNot reportedNot reported
Low Neutrophils
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)7Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)5Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)4Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)7Not reportedNot reportedNot reportedNot reported
Low platelets
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)8Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)3Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)5Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)7Not reportedNot reportedNot reportedNot reported
Low white Blood Cells
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)5Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)5Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)4Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)6Not reportedNot reportedNot reportedNot reported
Mucositis
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)1Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)1Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)1Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)3Not reportedNot reportedNot reportedNot reported
Nausea/Vomiting
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)8Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)8Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)9Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)9Not reportedNot reportedNot reportedNot reported
Oral Problems
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)3Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)2Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)4Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)9Not reportedNot reportedNot reportedNot reported
Other
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)4Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)4Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)7Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)7Not reportedNot reportedNot reportedNot reported
Other GI Problems
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)8Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)6Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)7Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)6Not reportedNot reportedNot reportedNot reported
Pain
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)9Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)6Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)7Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)7Not reportedNot reportedNot reportedNot reported
Peripheral/Sensory Neuropathy
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)11Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)11Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)8Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)10Not reportedNot reportedNot reportedNot reported
Pneumothorax
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)0Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)1Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Raised CA19-9
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)0Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)0Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)2Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Raised Blood Counts
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)1Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)1Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)1Not reportedNot reportedNot reportedNot reported
Rash
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)4Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)2Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)3Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)4Not reportedNot reportedNot reportedNot reported
Stomatitis
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)0Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)2Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)1Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)0Not reportedNot reportedNot reportedNot reported
Taste Alteration
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)3Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)2Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)1Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)2Not reportedNot reportedNot reportedNot reported
Urinary Problems
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)1Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)0Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)1Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)2Not reportedNot reportedNot reportedNot reported
Vaginal Bleeding
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)0Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)1Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)1Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)2Not reportedNot reportedNot reportedNot reported
Weight Gain
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)0Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)1Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)1Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)2Not reportedNot reportedNot reportedNot reported
Weight Loss
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (Carboplatin and Paclitaxel)2Not reportedNot reportedNot reportedNot reported
Arm II (Oxaliplatin and Capecitabine)3Not reportedNot reportedNot reportedNot reported
Arm III (Carboplatin, Paclitaxel, Bevacizumab)4Not reportedNot reportedNot reportedNot reported
Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)5Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        8
      2. group Id
        OG001
        value
        10
      3. group Id
        OG002
        value
        10
      4. group Id
        OG003
        value
        10
    title
    Abnormal lab values
  2. categories
    1. measurements
      1. group Id
        OG000
        value
        3
      2. group Id
        OG001
        value
        1
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        4
    title
    Allergic reaction
  3. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        1
      3. group Id
        OG002
        value
        1
      4. group Id
        OG003
        value
        1
    title
    Allergic rhinitis
  4. categories
    1. measurements
      1. group Id
        OG000
        value
        11
      2. group Id
        OG001
        value
        1
      3. group Id
        OG002
        value
        9
      4. group Id
        OG003
        value
        5
    title
    Alopecia
  5. categories
    1. measurements
      1. group Id
        OG000
        value
        12
      2. group Id
        OG001
        value
        7
      3. group Id
        OG002
        value
        4
      4. group Id
        OG003
        value
        6
    title
    Anemia
  6. categories
    1. measurements
      1. group Id
        OG000
        value
        1
      2. group Id
        OG001
        value
        1
      3. group Id
        OG002
        value
        3
      4. group Id
        OG003
        value
        5
    title
    Bleeding
  7. categories
    1. measurements
      1. group Id
        OG000
        value
        2
      2. group Id
        OG001
        value
        3
      3. group Id
        OG002
        value
        7
      4. group Id
        OG003
        value
        6
    title
    Cold-like symptoms
  8. categories
    1. measurements
      1. group Id
        OG000
        value
        3
      2. group Id
        OG001
        value
        4
      3. group Id
        OG002
        value
        7
      4. group Id
        OG003
        value
        9
    title
    Constipation
  9. categories
    1. measurements
      1. group Id
        OG000
        value
        5
      2. group Id
        OG001
        value
        6
      3. group Id
        OG002
        value
        5
      4. group Id
        OG003
        value
        8
    title
    Diarrhea
  10. categories
    1. measurements
      1. group Id
        OG000
        value
        2
      2. group Id
        OG001
        value
        1
      3. group Id
        OG002
        value
        3
      4. group Id
        OG003
        value
        0
    title
    dyspnea
  11. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        1
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        0
    title
    Edema Limbs
  12. categories
    1. measurements
      1. group Id
        OG000
        value
        10
      2. group Id
        OG001
        value
        10
      3. group Id
        OG002
        value
        8
      4. group Id
        OG003
        value
        11
    title
    Fatigue
denoms
  1. counts
    1. group Id
      OG000
      value
      13
    2. group Id
      OG001
      value
      13
    3. group Id
      OG002
      value
      13
    4. group Id
      OG003
      value
      11
    units
    Participants
description
Grade 1 or higher non-serious adverse events were graded by CTC AE v 4.
groups
  1. description
    Patients receive carboplatin IV over 30-60 minutes on day 1 and paclitaxel IV over 3 hours on day 1. Treatment repeats every 3 weeks for 6 courses in the absence of disease progression or unacceptable toxicity. Carboplatin: Given IV Laboratory Biomarker Analysis: Correlative studies Paclitaxel: Given IV Quality-of-Life Assessment: Ancillary studies
    id
    OG000
    title
    Arm I (Carboplatin and Paclitaxel)
  2. description
    Patients receive oxaliplatin IV over 2-6 hours on day 1 and capecitabine PO BID on days 1-14. Treatment repeats every 3 weeks for 6 courses in the absence of disease progression or unacceptable toxicity. Capecitabine: Given PO Laboratory Biomarker Analysis: Correlative studies Oxaliplatin: Given IV Quality-of-Life Assessment: Ancillary studies
    id
    OG001
    title
    Arm II (Oxaliplatin and Capecitabine)
  3. description
    Patients receive carboplatin and paclitaxel IV as in arm I and bevacizumab IV over 30-90 minutes on day 1. Treatment repeats every 3 weeks for 6 courses in the absence of disease progression or unacceptable toxicity. Patients then receive bevacizumab IV over 30-90 minutes alone on day 1. Treatment repeats every 3 weeks for 12 courses in the absence of disease progression or unacceptable toxicity. Bevacizumab: Given IV Carboplatin: Given IV Laboratory Biomarker Analysis: Correlative studies Paclitaxel: Given IV Quality-of-Life Assessment: Ancillary studies
    id
    OG002
    title
    Arm III (Carboplatin, Paclitaxel, Bevacizumab)
  4. description
    Patients receive oxaliplatin and capecitabine as in arm II, and bevacizumab as in arm III. Bevacizumab: Given IV Capecitabine: Given PO Laboratory Biomarker Analysis: Correlative studies Oxaliplatin: Given IV Quality-of-Life Assessment: Ancillary studies
    id
    OG003
    title
    Arm IV (Oxaliplatin, Capecitabine, Bevacizumab)
param Type
COUNT_OF_PARTICIPANTS
population Description
Eligible and treated patients
reporting Status
POSTED
time Frame
Every cycle while on treatment, up to 5 years
title
Participants With Grade 1 or Higher Non-serious Adverse Effects Assessed by CTCAE Version 4.0
type
SECONDARY
unit Of Measure
Participants

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice