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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1130579 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
# `1 ^3 |3 O7 sNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
0 ]4 h# r- ~1 `2 ?* t5 J+ Author Affiliations
1 J5 b  f- Y7 s& ^% ~4 J$ G. v5 a, t8 p, f: G8 U+ t0 C; u
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
, ~+ n- o2 E6 G  h6 \- ]2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
, q% y3 K- b; |: p: O* v3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
1 ?, J2 G) T3 ~( `8 a3 o7 H4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
( A) q9 C" x* t3 ~% J9 x4 d5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan % @8 o3 Z! S, s( R4 V- \2 q
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 1 q0 F5 p% [2 F5 ~
7Kinki University School of Medicine, Osaka 589-8511, Japan . s- J5 R; O8 L% f- Q9 r
8Izumi Municipal Hospital, Osaka 594-0071, Japan 7 v# S; }! `8 n* S9 _: S, V
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
" j3 R$ a( V) |Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp ; S) w' `4 e* e4 r1 v, r
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. 4 ]" c+ u) p% `7 z9 s0 y, o

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type , w7 N- l$ p- \9 E: U) i; t

6 t( l$ K; x; L2 E$ h: v, |/ g- iAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato / f  k2 _( k9 ~. M, o9 V  g

8 ~9 ~( y, s( p4 o8 X9 C  DAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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Published online on: Thursday, December 1, 2011
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" `) A9 `4 E. f6 `7 ?Doi: 10.3892/ol.2011.507 2 c& {* N9 H0 n
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Pages: 405-410
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! K5 ~. l4 f! k: `Abstract:
9 W4 c8 Y1 e; i! s* Q" j# iS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.  y1 Y  ]/ W# v6 |; I* R8 H. O

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population" S. T' n0 O) s! q- b
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
( t1 l# @, m8 m0 ?, x% o7 |+ Author Affiliations# o$ b, y* L, y! f
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
5 g4 R& N) X$ C0 O* H+ e2Department of Thoracic Surgery, Kyoto University, Kyoto 6 ^1 _& c: c4 W8 Q
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
1 l/ u) c5 v* ~8 O; h# E&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp 2 [( M. X4 z; o# n
Received September 3, 2010. 4 F7 Z; ^# X9 {1 Y' H
Revision received November 11, 2010.
- W* Z) |5 n( C7 ~3 _0 GAccepted November 17, 2010.
& x' L- j! c- x; B4 oAbstract/ C0 m; x9 A3 g) N" `  _5 a4 D5 m
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
4 F) e- T# c2 cPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. # e1 a: [% ?# k: G( {5 u
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
) ^: [4 o+ }/ P2 J& k1 }6 @: H4 p6 wConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。& z& E5 h8 n+ i) r* [6 ^( o
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?! d6 t+ o# A( M  b. `
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
7 y5 L/ a. ~$ _6 Jhttp://clinicaltrials.gov/ct2/show/NCT01523587# k6 @1 E2 {; ]1 ^: @1 F4 O
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC$ \/ }9 `0 ]; V% D& H) B
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。" V4 L9 p7 g/ Q9 M) V% D+ g# t$ e
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
7 Z. P2 a7 y& c% G4 a- `9 B从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
3 x& @- ^0 n* w& I1 t至今为止,未出 ...

6 z$ h( O$ c5 ^1 [没有副作用是第一追求,效果显著是第二追求。$ t0 ^0 ]6 y6 M( J% P! d
不错。

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