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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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1398300 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
; q2 e. o3 A, U) c& k( o0 p: {# oNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
# ~; z& {( W% d+ Author Affiliations
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) N; w( i( [/ k4 W6 d1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
6 p0 Q. N" X2 s" p, j% J2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan / T, N* x: R2 U3 {1 A( c7 h
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 8 A/ F* A3 h; m9 _. k
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
0 |# }! T$ {2 t5 f5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ' I% E( u, r! c6 n$ |
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
; L2 |! g% m* R6 h/ i; ?7Kinki University School of Medicine, Osaka 589-8511, Japan - `# x; ^- F8 P. F8 k( Z: f
8Izumi Municipal Hospital, Osaka 594-0071, Japan % ]  W2 H* k: d  p$ U) A) r
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 1 M7 Q( Q0 E7 `% n: V( n, z
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
9 h" [' [0 Q) u2 C# J1 @# qAbstractBackground: 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. + j4 N5 V5 h$ j+ g  e! E" i
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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 - S. E0 s& L* h# |$ |- K( T
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ( H) ]  N8 Z. }- ^3 y' P% P( o

& W6 G, g3 @1 S' LAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  6 i+ E( f- A' f
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Published online on: Thursday, December 1, 2011 4 l+ O/ m* m  B$ \5 ]
0 s7 C$ L) N5 B0 Z$ r* u7 a
Doi: 10.3892/ol.2011.507
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Pages: 405-410   R) a0 p1 C+ q. x( p8 V
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Abstract:- J2 ^, ]& x4 a8 i
S-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.# B3 a; [" n% l. ~8 {: }

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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
9 k7 p7 g- j% s& h. rF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 # M- F" e" ~2 x8 C* l) a
+ Author Affiliations- Q8 F5 |8 y5 i
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ' w# @3 e( q$ `2 F2 e7 X
2Department of Thoracic Surgery, Kyoto University, Kyoto
0 T" T+ p, J( J% @7 S1 g5 u3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
+ D' a+ P& i0 U" g: r3 ~6 d, J: P&#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
( @: e; Z" R+ N! S) o5 W2 vReceived September 3, 2010.
# a; P  L9 w- {, V. g# @+ Y  KRevision received November 11, 2010.
+ P2 T& g) k3 L2 J# F1 IAccepted November 17, 2010. - I; ?. M% ]- M2 E  N9 s
Abstract
8 J" t) K/ X$ I5 s: K* g1 w+ q4 T' }5 }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. ) R& X2 E! t" C/ ~
Patients 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. & u+ C' R( ?% N/ }
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.
$ }5 V  D; C7 b' |3 b2 O5 \' xConclusion: 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。, w. _% X- L) ?' H3 H+ L1 g) A
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?+ Y% g9 L5 ]4 F. J' c1 l
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
& g; ?+ D6 n) U2 Zhttp://clinicaltrials.gov/ct2/show/NCT015235875 f& j: M1 L- [
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
! v( h2 m$ D, ]* F0 G0 Q3 Ehttp://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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* L' P$ {7 D% }4 O5 Y+ Z( r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。0 D% o9 q2 X9 w# x& {- W1 \# ]7 Z
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
6 ]% M/ B7 i9 P* G. s- Z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。; \4 U4 D+ S, N* ?* g0 i% v
至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。
4 ]5 Y; T1 _3 E$ z. p9 v: e* `不错。

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