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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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1461000 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; l. N1 @; S6 `3 v
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 , T# \) C1 V/ M- S: m) f! Q
+ Author Affiliations& Y9 C' ?" h1 Y, m

# }% E) @* y& I$ }, ~& n9 h1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
( B% J. U+ r# \/ ~( p2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
, ~$ \' k  ]+ ]# q3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
8 j+ Y; h. o! y) e) k$ z* M% c$ c6 {4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 4 C5 V* r+ x9 A+ ]% y2 `
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 5 g7 w3 |% B$ E, W3 q
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 2 g; B& g& J. J5 x
7Kinki University School of Medicine, Osaka 589-8511, Japan
4 h% A  d3 Z2 U4 [" z1 j) V0 g* U8Izumi Municipal Hospital, Osaka 594-0071, Japan
7 g  w. c/ I/ R! i& b9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan " L% ~7 Y' q0 r( l8 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 / _5 c7 e  M" J1 d$ [) `2 h5 o) M4 N
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. 7 E& g3 p) ?: A$ p
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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 # l2 c9 F8 U1 n7 O) N4 a! k9 e6 e" M
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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
8 A7 M3 l7 r! Z
! e8 \/ \+ N: u+ t, n# ?9 qAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
6 Y9 z& B3 n. r2 B, j( V$ J" |( Z) Z, |) g6 {( k7 E
Published online on: Thursday, December 1, 2011
  j. z% {7 r) l; P% Y! c0 ?
' N% x  R+ C1 F! r1 E) h* d. EDoi: 10.3892/ol.2011.507 7 V6 i) m8 z& I) e. N" ~

0 n; E' X$ q$ C0 ?& w& E& _5 z7 yPages: 405-410
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( c* n7 R7 F6 i4 qAbstract:
/ q7 B7 n9 t. q/ C- lS-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.
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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
$ M/ e8 m9 `3 o6 Z# DF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3   }0 _# e' w1 t1 y. U/ i% B
+ Author Affiliations. D! L# W% ^8 }
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu # T% z1 ~: g& p9 @3 z7 `5 x9 r
2Department of Thoracic Surgery, Kyoto University, Kyoto
# J) F: q& N6 C9 p3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 9 {7 M+ p0 H; u
&#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" {* s3 u: B% f6 O# qReceived September 3, 2010. 6 C7 ]" f7 Y% W# F( B: m7 U6 L
Revision received November 11, 2010.
) h( s3 |+ l4 B9 n& m7 XAccepted November 17, 2010. - c. v, `9 p7 k3 ^) R; t4 m: c$ q& l
Abstract- o4 n/ e2 o# ^* s
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.
" e+ c. K& T7 v) v1 Z( FPatients 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.
6 o, D, [. Y6 o& @0 ]- HResults: 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.
0 b# z% q# F- `* g/ qConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 0 T* `* d5 l5 u" a- T
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。
1 {, y* B3 r' p' B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?% b& [: l' r) h
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
) q6 {7 g$ h+ X# Y; j# Phttp://clinicaltrials.gov/ct2/show/NCT01523587
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! i* u0 ~4 H0 t5 S. xBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC! d, N- F# d4 R2 w
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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& O% K8 c! i( b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。
8 l4 D) k' }$ N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
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没有副作用是第一追求,效果显著是第二追求。5 B" e0 f" h" G
不错。

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