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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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1089325 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
' X, X- z+ T8 K* v2 l9 C, KNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
4 f! q1 S1 Z$ R4 W+ Author Affiliations! j" R$ h; ?# u- L
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan . d3 }, L9 K/ o# t: d3 k
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
! F2 J6 v6 ^* X6 w1 n) n3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan * Z5 y5 l  h( ^: E- h- F
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
0 r8 a: \7 C8 ^5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
6 P$ p; N. F( [7 s* F- L6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
5 b9 y4 k2 i; H. P" y7Kinki University School of Medicine, Osaka 589-8511, Japan
3 {! y) Y+ Y  p! G- b1 @. Z7 m4 r8Izumi Municipal Hospital, Osaka 594-0071, Japan
" ]$ j& x: t+ k; _& U9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
* y3 ~  j4 U: k1 b- o" eCorrespondence 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 & c+ W+ U9 Y& H& r6 [) _
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 ! Z1 P4 Q, p" ?9 z. W0 v; u
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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
# B8 f+ V: S4 s& F6 _. x6 V
3 d9 ]( l3 e$ x" |Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan    V6 C0 _$ \  y; L% g

' W) x8 v" G" \/ K5 `% `Published online on: Thursday, December 1, 2011 - D% I  ^( i2 a/ p' D7 X) F- l5 G
2 O" a1 n$ z( s; T
Doi: 10.3892/ol.2011.507
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Pages: 405-410 ' J$ h$ R3 X7 f3 R- ]2 k* M

- X0 ?  g, o9 D" z# }! f9 uAbstract:
4 z& W  K+ j6 q$ T! h, Z% Y( wS-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.% G; j0 ^* n9 T& j* V

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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
2 `: W0 Z+ w7 |4 M4 p% h+ [' WF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
; [5 z$ b% C% J  v: t/ H7 q$ M+ Author Affiliations
; W0 c9 ?8 T, S5 d# H( S3 P1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu # i/ F/ {; _3 j0 R+ K8 N
2Department of Thoracic Surgery, Kyoto University, Kyoto 9 t  p& t5 G" G" ?9 l- D
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
7 J( n& s" ?& w6 O, x# t8 O: F&#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 . l7 l  C$ W4 R& D
Received September 3, 2010.
1 R$ Z6 ]* P. a, n9 t7 s8 V3 }Revision received November 11, 2010.
# |5 d: J! c4 FAccepted November 17, 2010. " k" i6 y4 y" i+ w
Abstract; @1 |) Z3 l& a6 H2 q7 w
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 s- W$ N" \+ pPatients 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. " h3 m# f1 o% ?1 q! 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.
9 b* e; ]7 Q  gConclusion: 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。- F: t9 ]( p; [2 |$ J' U. x( U0 _
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?! r. [: t. g4 h/ y) n
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 Chemotherapy1 k( `/ |* v" z" ?3 \
http://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC  A: I# n  N/ Q+ {7 T" C& J
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 $ i) F( y  i9 }

3 T, C* Q9 E6 K$ H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。+ b) g, K) G3 t! Y; j5 H, Y' M* 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* x  Z. F- r, ^1 N- ~: s+ o$ d
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。
' D; L$ j# ~! z1 x! t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。5 v. K5 Z4 N- w
不错。

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