Abstract | BACKGROUND: METHODS: RESULTS: Sixteen patients were enrolled in a 3-year pre-planned registration period. This study was prematurely closed due to poor patient accrual. The ORR and disease control rate were 6.7% (95% CI, 0.2-32.0) and 53.3% (95% CI, 26.6-78.7). The median PFS and overall survival (OS) were 2.4 months (95% CI, 0.0-5.2) and 9.7 months (95% CI, 8.2-11.2), respectively. The most frequently reported grades 3-4 adverse events were neutropenia (40%), anemia (27%), anorexia (33%), and fatigue (33%). CONCLUSION:
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Authors | Yasuyuki Kawamoto, Satoshi Yuki, Takashi Meguro, Kazuteru Hatanaka, Minoru Uebayashi, Michio Nakamura, Hiroyuki Okuda, Ichiro Iwanaga, Takashi Kato, Shintaro Nakano, Atsushi Sato, Kazuaki Harada, Koji Oba, Yuh Sakata, Naoya Sakamoto, Yoshito Komatsu |
Journal | The oncologist
(Oncologist)
Vol. 27
Issue 5
Pg. 340-e374
(05 06 2022)
ISSN: 1549-490X [Electronic] England |
PMID | 35303078
(Publication Type: Clinical Trial, Phase II, Journal Article)
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Copyright | © The Author(s) 2022. Published by Oxford University Press. |
Chemical References |
- Irinotecan
- Receptor, ErbB-2
- Trastuzumab
|
Topics |
- Antineoplastic Combined Chemotherapy Protocols
(adverse effects)
- Breast Neoplasms
(drug therapy)
- Female
- Humans
- Irinotecan
(therapeutic use)
- Receptor, ErbB-2
(metabolism)
- Stomach Neoplasms
(drug therapy, genetics)
- Survival Rate
- Trastuzumab
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