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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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1209976 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, A* a! j6 k# A, }8 M5 l# ^
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
% d6 Z" R, }2 @# W+ Author Affiliations1 h8 [) s' O% w( ^' g

$ z1 ~% B( x. b' }1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
- U% q5 R9 _" a) r2 h2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 0 p3 D4 x0 N. P. G
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
: f2 Z. j) Q: i/ a1 _# Y4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 1 P: N) t) S/ r% i" S
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ' A# S+ l# e: ^# ~
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
& l; B( ~$ J( N8 B7Kinki University School of Medicine, Osaka 589-8511, Japan
$ j- e! w- c- S, Z: @6 T% M7 X3 U8Izumi Municipal Hospital, Osaka 594-0071, Japan - w7 ~" G$ b2 x# ^* o4 V8 @
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
& }6 N) x1 N! j# uCorrespondence 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
. w4 ^9 W, V/ R0 n, q" V/ I9 f$ GAbstractBackground: 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.
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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 , F" Q1 [3 v1 C# O1 P' O

9 m& y; b8 Y5 i7 pAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ' B, N5 V) t; m( L
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Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  : V- K% [, o5 S0 x+ @. b/ x
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Published online on: Thursday, December 1, 2011 6 |% o$ O+ ~6 ?+ m

5 G# F- ~: ]7 S/ O0 R/ f) h  zDoi: 10.3892/ol.2011.507 + L# z" N, X- c* z/ P
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Pages: 405-410 / p; k) X* l! M+ X
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Abstract:9 d0 R9 r# ^4 Q% B: g
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.
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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 population3 W) `5 J2 P5 y( {
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
" j7 H- q, L4 I0 i8 U! W+ Author Affiliations
" X/ `; G' \6 S7 ]5 o7 a, K1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
3 T# u9 e/ D: r$ Y: n2Department of Thoracic Surgery, Kyoto University, Kyoto
) K* B9 K, b  b* p" p3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan , f5 }+ g0 f1 @; B" J
&#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 $ M! N* B! v1 z8 n4 o0 o6 R) b
Received September 3, 2010.
$ \& x$ Z, Q6 y& F/ s0 fRevision received November 11, 2010. % \& k+ T( U5 X' |# n- a
Accepted November 17, 2010. 9 e1 s0 L! G+ K
Abstract% o1 X6 m  X0 k$ j( F3 v0 O# 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 o: v8 A$ z) ~1 R' KPatients 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. 4 D$ q4 G1 _* b* t/ {4 s
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. / J5 H3 c. {2 [
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. , v1 c! G, p; d. ~5 R$ _
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。
5 J4 v& t) x- o5 @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?0 J- x5 Y, u, }% t1 u; ]: z
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- U" J4 s' a3 C. T6 ?/ N6 y. V
http://clinicaltrials.gov/ct2/show/NCT015235877 N8 N5 q$ \2 V! ?

9 E" W6 u/ b3 `! X3 ^- u7 {4 G! XBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC' D# Y  Y& r8 @& O4 \1 Q  e9 [: R7 `
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 * M% W7 ^' y/ I2 E& w
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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。
% U: r7 H4 ~+ i% E1 X* I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
% c8 J9 S5 A, E2 O2 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。
( L. i* f, R9 y6 x3 k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。
8 }: r. r: K7 a  ~  V6 j不错。

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