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. 2013 Nov 12;10(2):e29–e36. doi: 10.1200/JOP.2013.001121

Table 2.

PCPs (n = 981) and Oncologists (n = 1,125) Reporting Awareness of LEs for Each Chemotherapy Agent*

LE Doxorubicin
Cyclophosphamide
Paclitaxel
Oxaliplatin
Fluorouacil
PCPs (%) Oncologists (%) P PCPs (%) Oncologists (%) P PCPs (%) Oncologists (%) P PCPs (%) Oncologists (%) P PCPs (%) Oncologists (%) P
Peripheral neuropathy 8 1 < .001 17 3 < .001 27 97 < .001 22 97 < .001 13 8 < .001
Pulmonary fibrosis 8 1 < .001 13 21 < .001 6 5 NS 9 5 < .001 2 2 NS
Cardiac dysfunction 55 95 < .001 7 8 NS 6 5 NS 1 0 NS 7 22 < .001
Premature menopause 7 67 < .001 15 71 < .001 13 31 < .001 2 15 < .001 3 15 < .001
Secondary malignancies 5 48 < .001 17 62 < .001 3 4 NS 2 4 .008 6 4 .03
Do not know 36 0.5 < .001 51 6 < .001 56 1 < .001 71 2 < .001 66 27 < .001

NOTE. For doxorubicin, main LE is cardiac dysfunction; for paclitaxel and oxaliplatin, main LE is peripheral neuropathy; for cyclophosphamide, main LEs are premature menopause and secondary malignancies (indicated by bold font).

Abbreviations: LE, late or long-term effect; PCP, primary care provider.

*

Total of 96 respondents (4%) skipped section (PCPs, n = 91; oncologists, n = 5).