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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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1350110 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
! v! P, i& i0 D9 E" W7 ONOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 & h3 ]6 w- l+ z
+ Author Affiliations& n0 Q/ e( v, g6 [

: j* T5 s! h9 i* w1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan + X. Z2 z$ ]5 F$ f9 W. y
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ; {- F3 E/ S6 J& n  E
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ' w: q2 ^, T8 W- Z0 ^& k7 V
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
: n. k+ }, g3 w5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ; k1 [$ O- z6 c" z5 s, s. A
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan / x! b! T  v% J# K- {" |
7Kinki University School of Medicine, Osaka 589-8511, Japan ) H7 X# S  h% x2 x9 ?
8Izumi Municipal Hospital, Osaka 594-0071, Japan
9 m4 I- j) u/ ^9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan , q4 V& w4 c) L6 M0 b/ c
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 ' b; p- d+ N  a$ i, ?3 w
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. - l" j. ]7 g# ]% 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 , T3 B, U# Q; B/ B
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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 7 W# D+ }* f" p1 g8 w# P( s

- M* B- T" o1 a3 M! K8 i- x/ fAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
! C- W: t1 w0 [5 a: r( v* B% v+ Q) [! U! u1 c1 o4 f
Published online on: Thursday, December 1, 2011 ) k: w+ C! b9 [$ M

5 R  Y9 n) l0 r1 r3 y9 i* nDoi: 10.3892/ol.2011.507
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. S' f: u( a- i: ?0 f% L/ PPages: 405-410 + E# y. Z6 u  D' S/ T6 q
2 i' C" K: B9 {
Abstract:
9 ~, m6 w8 e# L9 b% US-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
- ^4 g  r0 m% m3 JF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
+ J5 c3 h+ v3 J& M+ Author Affiliations9 e- o) q2 j9 @; s* b0 r  S
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu   Q2 |  S' q9 c$ _$ M9 ?0 u+ J
2Department of Thoracic Surgery, Kyoto University, Kyoto
! T7 F" Z+ Y: P8 Y: g3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
: _4 F; ^- ~2 t6 |5 E! d2 z+ N  i&#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
" _- }* p3 R% W& _6 WReceived September 3, 2010.
: `0 X8 U9 U6 v, yRevision received November 11, 2010.
5 E" h" I& w/ W( V$ eAccepted November 17, 2010.
7 ]8 i' Y+ U* o% LAbstract9 I! D& u3 k* X' A. I
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.
2 J, D3 L3 c% O2 H1 T5 u& i7 a) bPatients 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.
0 i4 Q# {$ B: B0 G% t$ XResults: 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.
# E  g" G( \# f8 j. f+ n- h4 cConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 4 ~% W% G7 m) D
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。
) z0 b! J7 B  {% C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?
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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 O# D6 H/ M% u1 |0 s9 ohttp://clinicaltrials.gov/ct2/show/NCT015235879 B7 }+ T% h2 }: g) S) n) X: C2 [

0 U3 K8 F) m6 h. W. G( ?BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC9 L; m) c0 r, {" ^  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 3 T5 Y7 G" X) M; S1 B

& W; c, M( b( Y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。
3 l1 P& E4 U8 L) x" w; F, j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

9 b+ B, }7 Q3 s# X* H& w9 N1 p1 f没有副作用是第一追求,效果显著是第二追求。2 P; H1 }( q' U" T* R8 `8 Y; k% |
不错。

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