Our Experience with Atezolizumab plus Bevacizumab for Unresectable Hepatocellular Carcinoma
We report our experience with atezolizumab plus bevacizumab for unresectable hepatocellular carcinoma.
METHODS: Fourteen patients with unresectable hepatocellular carcinoma treated with atezolizumab plus bevacizumab at our department were retrospectively evaluated for antitumor efficacy and adverse events.
RESULTS: Age ranged from 66-91 years(median 77.5 years), 11 males and 3 females, number of doses ranged from 2-26(median 13), and observation period ranged from 31-790 days (median 427 days). Antitumor efficacy was CR in 3 patients, PR in 3, SD in 6, and PD in 2. One patient with PD died 650 days after the start of treatment, but the others are still alive. Adverse events included proteinuria in 9 patients who discontinued bevacizumab, hypothyroidism requiring levothyroxine sodium hydrate in 7 patients, dermatitis in 2 patients, and colitis requiring hospitalization in 2 patients.
DISCUSSION: Despite the small number of cases, a high antitumor effect was observed with a CR rate of 21%. Although proteinuria and hypothyroidism were observed relatively frequently as adverse events, they were easily controlled and did not pose a major clinical problem.
Medienart: |
Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:50 |
---|---|
Enthalten in: |
Gan to kagaku ryoho. Cancer & chemotherapy - 50(2023), 13 vom: 02. Dez., Seite 1513-1515 |
Sprache: |
Japanisch |
---|
Beteiligte Personen: |
Shimizu, Junzo [VerfasserIn] |
---|
Themen: |
2S9ZZM9Q9V |
---|
Anmerkungen: |
Date Completed 05.02.2024 Date Revised 05.02.2024 published: Print Citation Status MEDLINE |
---|
Förderinstitution / Projekttitel: |
|
---|
PPN (Katalog-ID): |
NLM367926865 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM367926865 | ||
003 | DE-627 | ||
005 | 20240205232122.0 | ||
007 | tu | ||
008 | 240202s2023 xx ||||| 00| ||jpn c | ||
028 | 5 | 2 | |a pubmed24n1281.xml |
035 | |a (DE-627)NLM367926865 | ||
035 | |a (NLM)38303325 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a jpn | ||
100 | 1 | |a Shimizu, Junzo |e verfasserin |4 aut | |
245 | 1 | 0 | |a Our Experience with Atezolizumab plus Bevacizumab for Unresectable Hepatocellular Carcinoma |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ohne Hilfsmittel zu benutzen |b n |2 rdamedia | ||
338 | |a Band |b nc |2 rdacarrier | ||
500 | |a Date Completed 05.02.2024 | ||
500 | |a Date Revised 05.02.2024 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a We report our experience with atezolizumab plus bevacizumab for unresectable hepatocellular carcinoma | ||
520 | |a METHODS: Fourteen patients with unresectable hepatocellular carcinoma treated with atezolizumab plus bevacizumab at our department were retrospectively evaluated for antitumor efficacy and adverse events | ||
520 | |a RESULTS: Age ranged from 66-91 years(median 77.5 years), 11 males and 3 females, number of doses ranged from 2-26(median 13), and observation period ranged from 31-790 days (median 427 days). Antitumor efficacy was CR in 3 patients, PR in 3, SD in 6, and PD in 2. One patient with PD died 650 days after the start of treatment, but the others are still alive. Adverse events included proteinuria in 9 patients who discontinued bevacizumab, hypothyroidism requiring levothyroxine sodium hydrate in 7 patients, dermatitis in 2 patients, and colitis requiring hospitalization in 2 patients | ||
520 | |a DISCUSSION: Despite the small number of cases, a high antitumor effect was observed with a CR rate of 21%. Although proteinuria and hypothyroidism were observed relatively frequently as adverse events, they were easily controlled and did not pose a major clinical problem | ||
650 | 4 | |a English Abstract | |
650 | 4 | |a Journal Article | |
650 | 7 | |a Bevacizumab |2 NLM | |
650 | 7 | |a 2S9ZZM9Q9V |2 NLM | |
650 | 7 | |a atezolizumab |2 NLM | |
650 | 7 | |a 52CMI0WC3Y |2 NLM | |
650 | 7 | |a Antibodies, Monoclonal, Humanized |2 NLM | |
700 | 1 | |a Yamashita, Masafumi |e verfasserin |4 aut | |
700 | 1 | |a Odagiri, Kazuki |e verfasserin |4 aut | |
700 | 1 | |a Takeyama, Hiroshi |e verfasserin |4 aut | |
700 | 1 | |a Yanagimoto, Yoshitomo |e verfasserin |4 aut | |
700 | 1 | |a Suzuki, Yozo |e verfasserin |4 aut | |
700 | 1 | |a Ikenaga, Masakazu |e verfasserin |4 aut | |
700 | 1 | |a Kawase, Tomono |e verfasserin |4 aut | |
700 | 1 | |a Imamura, Hiroshi |e verfasserin |4 aut | |
700 | 1 | |a Dono, Keizo |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Gan to kagaku ryoho. Cancer & chemotherapy |d 1993 |g 50(2023), 13 vom: 02. Dez., Seite 1513-1515 |w (DE-627)NLM012601861 |x 0385-0684 |7 nnns |
773 | 1 | 8 | |g volume:50 |g year:2023 |g number:13 |g day:02 |g month:12 |g pages:1513-1515 |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 50 |j 2023 |e 13 |b 02 |c 12 |h 1513-1515 |