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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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1288244 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
/ I! ~" [  D4 O% G% k* {6 uNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
/ k/ B' V6 U0 U" A# y) x3 |  i1 R" ~+ Author Affiliations: }+ F0 W3 y" \$ i7 N9 x9 ^0 U% \

1 H4 M' t: T* C" a1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ' n* l2 l0 b. x1 h
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
8 O- n: x8 U7 y7 n3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan . z  `# E+ B) M( L, F
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
) V2 P( C8 O6 H! X8 _5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ; Z7 _: ~3 }3 ]; W4 D
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
8 _, w" K& f8 t1 C; z5 a: \2 W7Kinki University School of Medicine, Osaka 589-8511, Japan
9 b+ M0 ?8 Z& m3 d2 a! v8Izumi Municipal Hospital, Osaka 594-0071, Japan " R5 Q# ?" [4 a8 ]4 a: p" @' O
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan : n0 j5 t5 h( H4 U& k/ U; Z9 J
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 + `( L5 ]6 k# \0 j! q
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.
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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 " ^3 I8 a2 Y) n

& ^0 S& `  P! Y, R! E6 IAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
* {  E9 `# W/ }- {; i  ^; E3 k) u
Affiliations: 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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" m# v/ i% I& _$ f6 D3 TPublished online on: Thursday, December 1, 2011 2 j. G" V/ s) H9 S+ B1 t9 d

3 _9 Z0 |; L! D9 j% j7 D9 UDoi: 10.3892/ol.2011.507 5 w* H& I3 p' b+ Q

- z5 h6 U$ B+ R# r9 mPages: 405-410 ' g9 S- b2 Q5 I$ b* t

, l% ]9 o- a8 x, D' }7 ~' hAbstract:
6 n1 P" V3 o/ R. a' z5 vS-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./ r9 x3 c; ~# S% n4 g4 `. q2 }
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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 population1 _0 M7 |+ f- z' l( x2 J$ k/ g
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 8 I/ A6 B) b7 G8 ?
+ Author Affiliations
8 d1 \  P) C4 B; R" o7 w3 Y7 ~1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
$ L1 I. d! {4 n) x* J& r2Department of Thoracic Surgery, Kyoto University, Kyoto : A4 R9 X- c& k( m7 z+ g
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 4 y* X; W4 U8 {% B* f0 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
0 e% M5 k% G% o% R  x# uReceived September 3, 2010. : C+ P4 `2 Q% P+ q6 L! z" o
Revision received November 11, 2010.
& m" T7 e3 i1 i( I9 Q3 lAccepted November 17, 2010. : F# T, E9 }4 b, e, v, g, ]% r
Abstract* r5 d) _0 o0 L0 t3 z5 K
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. - W$ ?7 Q2 a* L8 E" d  _
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. / b+ t. Q$ x) k3 f, ^* y4 A
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. ( p# k' d7 k" o
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 2 _: ^+ B" [8 B8 V7 L
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。
! x* ~4 v/ V. T1 D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. z; f7 n# U& o
http://clinicaltrials.gov/ct2/show/NCT015235878 x& O. {- ~8 |! s

6 A+ R$ j* m7 m; a# r0 \; DBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
/ o1 A5 r# }3 {, f7 ^: Uhttp://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 + Y, h! E8 b/ B

# ^& z3 ~/ W6 h5 C0 ?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。
& ~9 g- x" \6 u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 $ n/ I& R9 D/ V+ `6 q( K) b* c: i
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。/ ]! B: ~4 l1 a4 B) a5 Z4 v3 i
至今为止,未出 ...
! ^8 K3 n0 U+ q1 p  x9 J
没有副作用是第一追求,效果显著是第二追求。
; c  C9 {' {+ V  P" M! c) @8 L( b不错。

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