Table 2.
Adverse Events | IP/IV arm (N = 106)a | IV arm (N = 107)b | P valuec |
---|---|---|---|
No. (%) | |||
Leukopenia | 57 (53.8) | 38 (35.2) | 0.006 |
Neutropenia | 70 (66.0) | 64 (59.3) | 0.305 |
anaemia | 25 (23.6) | 6 (5.6) | <0.001 |
Platelet count < 50*10^9 | 13 (12.3) | 8 (7.5) | 0.241 |
Gastrointestinal event | 11 (10.4) | 2 (1.9) | 0.010 |
Infection | 12 (11.3) | 5 (4.7) | 0.073 |
Thromboembolic event (Grade 5) | 1 (0.9)d | 0 (0) | 0.498 |
a 3 patients in IP group did not receive IV chemotherapy.
b 1 patients did not receive any protocol-based therapy. 1 patient only received 3 cycles of IV therapy after cytoreduction and the data of adverse events were missed.
cP values were calculated by χ2-test (grades 0, 1, and 2 vs. grades 3 and 4).
d 1 patient died of mesenteric venous thrombosis after completing 4 cycles of IP therapy and 4 cycles of IV therapy. In the intraperitoneal chemotherapy group, other 3 patients encountered grade 2 thromboembolic events (deep venous thrombosis of the lower extremities). And in the intravenous chemotherapy group, 1 patient encountered a grade 2 thromboembolic event (Upper-extremity deep vein thrombosis), which was PICC line-associated thrombosis31